247 results on '"Katsuma S"'
Search Results
2. Interspecies linkage analysis of mo, a Bombyx mori locus associated with mosaicism and gynandromorphism
- Author
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Fujii, T., Abe, H., Yamamoto, K., Katsuma, S., and Shimada, T.
- Published
- 2011
- Full Text
- View/download PDF
3. Functional characterization of chitinase from Cydia pomonella granulovirus
- Author
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Daimon, T., Katsuma, S., Kang, W. K., and Shimada, T.
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- 2007
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4. Reduced cysteine protease activity of the hemolymph of Bombyx mori larvae infected with fp25K-inactivated Bombyx mori nucleopolyhedrovirus results in the reduced postmortem host degradation
- Author
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Katsuma, S., Tanaka, S., Shimada, T., and Kobayashi, M.
- Published
- 2004
- Full Text
- View/download PDF
5. Genomic analysis of a mouse model of immunoglobulin A nephropathy reveals an enhanced PDGF–EDG5 cascade
- Author
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Katsuma, S, Shiojima, S, Hirasawa, A, Suzuki, Y, Takagaki, K, Murai, M, Kaminishi, Y, Hada, Y, Koba, M, Muso, E, Miyawaki, S, Ohgi, T, Yano, J, and Tsujimoto, G
- Published
- 2001
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6. Molecular characterization of baculovirus Bombyx mori nucleopolyhedrovirus polyhedron mutants
- Author
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Katsuma, S., Noguchi, Y., Shimada, T., Nagata, M., Kobayashi, M., and Maeda, S.
- Published
- 1999
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- View/download PDF
7. Electrochemical Characterization of Ti and Ti Base Alloys under Simulated Body Fluid Environment
- Author
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Fujimoto, Shinji, primary, Kusu, H., additional, Katsuma, S., additional, Sakamoto, Masashi, additional, and Tang, Y.C., additional
- Published
- 2006
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8. CenH3-independent kinetochore assembly in Lepidoptera requires CENP-T
- Author
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Cortes-Silva, N, primary, Ulmer, J, additional, Kiuchi, T, additional, Hsieh, E, additional, Cornilleau, G, additional, Ladid, I, additional, Dingli, F, additional, Loew, D, additional, Katsuma, S, additional, and Drinnenberg, IA, additional
- Published
- 2019
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- View/download PDF
9. Mapping and recombination analysis of two moth colour mutations, Black moth and Wild wing spot, in the silkworm Bombyx mori
- Author
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Ito, K, primary, Katsuma, S, additional, Kuwazaki, S, additional, Jouraku, A, additional, Fujimoto, T, additional, Sahara, K, additional, Yasukochi, Y, additional, Yamamoto, K, additional, Tabunoki, H, additional, Yokoyama, T, additional, Kadono-Okuda, K, additional, and Shimada, T, additional
- Published
- 2015
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10. Identification and functional analysis of a Masculinizer orthologue in Trilocha varians (Lepidoptera: Bombycidae)
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Lee, J., primary, Kiuchi, T., additional, Kawamoto, M., additional, Shimada, T., additional, and Katsuma, S., additional
- Published
- 2015
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11. Identification and characterization of the fusion transcript, composed of the apterous homolog and a putative protein phosphatase gene, generated by 1.5-Mb interstitial deletion in the vestigial (Vg) mutant of Bombyx mori
- Author
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Fujii, T., primary, Abe, H., additional, Katsuma, S., additional, and Shimada, T., additional
- Published
- 2011
- Full Text
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12. Role of the ubiquitin-proteasome system in Bombyx mori nucleopolyhedrovirus infection
- Author
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Katsuma, S., primary, Tsuchida, A., additional, Matsuda-Imai, N., additional, Kang, W., additional, and Shimada, T., additional
- Published
- 2010
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13. Mass identification of transcriptional units expressed from the Bombyx mori nucleopolyhedrovirus genome
- Author
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Katsuma, S., primary, Kang, W., additional, Shin-i, T., additional, Ohishi, K., additional, Kadota, K., additional, Kohara, Y., additional, and Shimada, T., additional
- Published
- 2010
- Full Text
- View/download PDF
14. Transgenic analysis of the BmBLOS2 gene that governs the translucency of the larval integument of the silkworm, Bombyx mori
- Author
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Fujii, T., primary, Daimon, T., additional, Uchino, K., additional, Banno, Y., additional, Katsuma, S., additional, Sezutsu, H., additional, Tamura, T., additional, and Shimada, T., additional
- Published
- 2010
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15. N-linked glycans located in the pro-region of Bombyx mori nucleopolyhedrovirus V-CATH are essential for the proper folding of V-CATH and V-CHIA
- Author
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Katsuma, S., primary, Nakanishi, T., additional, Daimon, T., additional, and Shimada, T., additional
- Published
- 2009
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16. Impact of punctual mutations in the cap gene of Junonia coenia densovirus (JcDNV) on virus assembly and infectivity to Ld 652 cells and Spodoptera littoralis larvae
- Author
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Iatrou, Kostas, Couble, Pierre, Abd-Alla, A., Jousset, F-X., Cousserans, F., Bergoin, M., Abe, H., Fujii, T., Mita, K., Ajimura, M., Shimada, T., Sahara, K., Tamura, T., Altstein, M., Hariton, A., Davidovitch, M., Ben-Aziz, O., Barat-Houari, M., Hilliou, F., Jousset, F.-X., Sofer, L., Deleury, E., Rocher, J., Ravallec, M., Galibert, L., Feyereisen, R., Fournier, P., Volkoff, A-N., Baxter, Simon W., Chamberlain, Nicola, Papa, Riccardo, Humphray, Sean J., ffrench-Constant, Richard H., McMillan, W. Owen, Jiggins, Chris D., Behere, G.T., Russell, D., Batterham, P., Tay, W. T., Beldade, P., Rudd, S., Gruber, J.D., Long, A.D., Breugelmans, B., Simonet, G., de Velde, S. Van, Soest, S. Van, Smagghe, G., Broeck, J. Vanden, Clark, R., Brown, S., Heckel, D., Jiggins, C. D., Collins, S., Vogler, A. P, Chamberlain, N., Baxter, S., Jiggins, C., ffrench-Constant, R.H., Chortyk, O., Friz, J., Thompson, C., Kumar, P., Tice, C., Vertin, B., Palli, R., Kumar, M., Meyer, A., Meteyer, T., Smith, H., Cress, D., Li, B., Hormann, R., Collinge, Derek, Gordon, Karl, Behm, Carolyn, Whyard, Steve, Alençon, d', Audant, E., Bernard-Samain, P., Bidegainberry, S., Brehélin, V., Brun-Barale, M., Cousserans, A., Duvic, C., Escoubas, B., Feyereisen, J-M., Fournier, R., Gagneur, Ph., Gordon, C., Gimenez, K., Heckel, S., Hotelier, D., Hilliou, Th., Mita, F., Negre, K., Sabourault, V., Suraporn, C., Volkoff, S., Weissenbach, N., Maria, De Simone Anna, Angela, Sorrentino, Francesca, Di Cara, Polito, Lino, Anna, Digilio F., Drezen, J-M, Bezier, A., Lesobre, J., Huguet, E., Dupuy, C., Eleftherianos, I., Millichap, P. J., Felföldi, G., Gökcen, F., Waterfield, N., Clarke, D. J., ffrench-Constant, R. H., Reynolds, S. E., Elias, M., Joron, M., Willmott, K., Kaiser, V., Silva-Brandão, K. L., Freitas, A.V.L., Arias Mejía, C., Gomez Pineres, L.M., Brower, A.V.Z., Escoubas, J.-M., Girard, P.-A., Volkoff, N., Boublik, Y., D'Alençon, E., Taillez, P., Brehélin, M., Venekei, I., Fischer, H. M., Wheat, C. W., Wittstock, U., Heckel, D. G., Vogel, H., Freitak, D., Katsuma, S., Futahashi, R., Fujiwara, H., Garel, Annie, Briolay, Jérôme, Brouilly, Patrick, Royer, Corinne, Sasanuma, Shun-ichi, Sasanuma, Motoe, Keime, Céline, Gandrillon, Olivier, Chavancy, Gérard, Mita, Kasuei, Geber, M., Faye, I., Terenius, O., Goldsmith, M., Proestou, D., Carter, D., Nicholson, E., Wu, C., Zhang, H., Gopinathan, K. P., Parthasarathy, R., Dhawan, S., Gordon, K., Colebatch, G., Campbell, P.M., Horne, I., East, P.D., Hughes, T.M., Marcus, J.M., Serbielle, C., Douris, V., Lalmanach, G., Iatrou, K., Iga, Masatoshi, Sekimoto, Takayuki, Elmogy, Mohamed, Iwami, Masafumi, Sakurai, Sho, Jacquin-Joly, E., Merlin, C., Malpel, S., Pelletier, J., Brigaud, I., François, M-C., Maïbèche, M., Jarvis, D.L., Aumiller, J.J., Geisler, C., Hensley, J., Hollister, J.R., Shi, X., Jiggins, Chris D, Joron, Mathieu, Mallet, James, Jostova, P., Svatos, A., Pichova, Iva, Kadono-Okuda, K., Ito, K., Nohata, J., Yamamoto, K., Sasanuma, M., Sasanuma, S., Eguchi, R., Hara, W., Kiyokawa, I., Kobayashi, I., Uchino, K., Sezutsu, H., Kanda, T., Miura, T., Ohashi, T., Katayama, K., Kourti, A., Gkouvitsas, T., Kusakabe, T., Mon, H., Takahashi, M., Lee, J.M., Kawaguchi, Y., Labropoulou, V., Stefanou, D., Magkrioti, C., Andronopoulou, E., Swevers, L., Lapointe, R., Tanaka, K., Barney, W., Whitfield, J., Banks, J., Béliveau, C., Stoltz, D., Webb, B.A., Cusson, M., Lee, Siu Fai, Heckel, David G., Li, Yi, Guarino, Linda A., Li, Muwang, Li, Minhui, Guo, Qiuhong, Miao, Xuexia, Hou, Chengxiang, Lin, Hongxuan, Huang, Yongping, Li, Lan, Zheng, Sichun, Ladd, Tim, Zhang, Dayu, Buhlers, Deborah, Krell, Peter J., Arif, Basil M., Retnakaran, Arthur, Feng, Qili, Doucet, Daniel, Machado, Ednildo, Swevers, Luc, Makhijani, Kalpana, Bharathi, V, Kannan, Ramakrishnan, Shashidhara, L S, Mauchamp, Bernard, Jalabert, Audrey, Rocha, Martine Da, Grenier, Anne-Marie, Labas, Valérie, Vinh, Joëlle, Mita, Kazuei, Kadono-Okuda, Keiko, Miao, Yungen, Yue, Wanfu, Li, Xinghua, Wu, Xiaofeng, Miller, T.A., Park, Y., Ren, X., Kasahara, M., Sasaki, S., Nagayasu, Y., Yamada, T., Kanamori, H., Namiki, N., Kitagawa, M., Yamashita, H., Yasukochi, Y., Rvikumar, G., Shimomura, M., Nagamura, Y., Shin-I, T., Morishita, S., Sasaki, T., Sugahara, R., Monteiro, Antónia, Chen, Bin, Ramos, Diane, Kamal, Firdous, Glaser, Gary, Stockslager, Steven, Nieberding, C., Schneider, V., Vos, H. De, Lassance, J.M., Lofstedt, C., Brakefield, P.M., Nighorn, A., Papanicolaou, A., Blaxter, M.L., Jiggins, C.D., Papantonis, A., Sourmeli, S., Lecanidou, R., Rocha, M. Da, Royer, C., Pennacchio, F., Falabella, P., Varricchio, P., Malva, C., Pohl, Nelida, Sison-Mangus, Marilou, Briscoe, Adriana D., Saenko, S.V., Satish, V., Shukla, J.N., Nagaraju, J., Frank, Scholz, Tine, Lesch, Susann, Beez, Traute, Holthusen, Ines, Anderl, Geuenich, Silvia, Tina, Trenczek, Kojima, K., Niimi, T., Hatakeyama, M., Shiotsuki, Takahiro, Tan, An-Jiang, Tamura, Toshiki, Simpson, Robert, Newcomb, Richard, Beuning, Lesley, Yauk, Yah-Khing, Crowhurst, Ross, Gatehouse, Heather, Gatehouse, Laurence, Markwick, Ngaire, Chagne, Dave, Gleave, Andrew, Christeller, John, Strand, M. R., Soin, T., Loocke, K. Van, Wheelock, C., Harada, T., Akamatsu, M., Nakagawa, Y., Truman, JW, Hiruma, K, Allee, JP, MacWhinnie, SGB, Champlin, D, Riddiford, LM, Turnbull, M.W., Vitkova, M., Kubickova, S., Marec, F., Kroymann, J., Mithöfer, A., Boland, W., Vogt, R.G., Franco, M-d., Bohbot, J, Fernandez, K., Kobres, P., Hanna, J., Poppy, J., Webb, Bruce A., Gill, Torrence A., Fath-Goodin, Angelika, Kroemer, Jeremy, Wedde, M., Altincicek, B., Vilcinskas, A., Wee, Choon Wei, Robin, Charles, Heckel, David G, Wheat, Christopher W., Labandeira, Conrad, Andolfatto, P., Feng, Q., Simpson, R., Vogel, Heiko, Williams, A. K., Xia, Qingyou, Zhou, Zeyang, Lu, Cheng, Xiang, Zhonghuai, Zhang, Liang, Yamamoto, Kimiko, Narukawa, Junko, Nohata, Junko, Suetsugu, Yoshitaka, Minami, Hiroshi, Shimomura, Michihiko, Yukuhiro, K., Itoh, M., Banno, Y., Kômoto, N., Kosegawa, E., Hirokawa, M., Tatematsu, K., Nishimura, M., Maekawa, H., Kawanishi, Y., Nakajima, Y., and Krell, Peter J
- Subjects
Article - Published
- 2007
17. Mapping and recombination analysis of two moth colour mutations, Black moth and Wild wing spot, in the silkworm Bombyx mori
- Author
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Ito, K, Katsuma, S, Kuwazaki, S, Jouraku, A, Fujimoto, T, Sahara, K, Yasukochi, Y, Yamamoto, K, Tabunoki, H, Yokoyama, T, Kadono-Okuda, K, and Shimada, T
- Abstract
Many lepidopteran insects exhibit body colour variations, where the high phenotypic diversity observed in the wings and bodies of adults provides opportunities for studying adaptive morphological evolution. In the silkworm Bombyx mori, two genes responsible for moth colour mutation, Bm and Ws, have been mapped to 0.0 and 14.7 cM of the B. mori genetic linkage group 17; however, these genes have not been identified at the molecular level. We performed positional cloning of both genes to elucidate the molecular mechanisms that underlie the moth wing- and body-colour patterns in B. mori. We successfully narrowed down Bm and Ws to ~2-Mb-long and 100-kb-long regions on the same scaffold Bm_scaf33. Gene prediction analysis of this region identified 77 candidate genes in the Bm region, whereas there were no candidate genes in the Ws region. Fluorescence in-situ hybridisation analysis in Bm mutant detected chromosome inversion, which explains why there are no recombination in the corresponding region. The comparative genomic analysis demonstrated that the candidate regions of both genes shared synteny with a region associated with wing- and body-colour variations in other lepidopteran species including Biston betularia and Heliconius butterflies. These results suggest that the genes responsible for wing and body colour in B. mori may be associated with similar genes in other Lepidoptera.
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- 2016
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18. Characterization of the 25K FP gene of the baculovirus Bombyx mori nucleopolyhedrovirus: implications for post-mortem host degradation.
- Author
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Katsuma, S, primary, Noguchi, Y, additional, Zhou, C L, additional, Kobayashi, M, additional, and Maeda, S, additional
- Published
- 1999
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19. Reduced cysteine protease activity of the hemolymph ofBombyx morilarvae infected withfp25K-inactivatedBombyx morinucleopolyhedrovirus results in the reduced postmortem host degradation.
- Author
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Katsuma, S., Tanaka, S., Shimada, T., and Kobayashi, M.
- Subjects
BACULOVIRUSES ,CYSTEINE proteinases ,SILKWORMS ,GENE expression ,HEMOLYMPH ,VIROLOGY - Abstract
We previously reported that the FP25K gene (fp25K) product of the baculovirusBombyx morinucleopolyhedrovirus (BmNPV) is involved in postmortem host degradation. Here, we investigated the mechanism by which reduced postmortem host degradation is caused after the infection offp25K-mutated BmNPVs. Firstly, we investigated gene expression levels ofvcathandchiAboth of which products are involved in postmortem host degradation. We found that transcriptional levels of these genes infp25K-mutated BmNPV-infected BmN cells were comparable to those in cells infected with wild-type (wt) BmNPV. Next, we examined the cysteine protease activity infp25K-mutated BmNPV-infected BmN cells. Although the cysteine protease activity in BmN cells infected withfp25K-mutated BmNPVs was comparable to that of wt BmNPV-infected cells, the released activity in the culture medium is dramatically reduced in that of cells infected withfp25Kmutants. We also found that the cysteine protease activity in the hemolymph offp25K-mutated BmNPV-infectedB. morilarvae is drastically reduced compared to that of wt BmNPV-infected larvae. These results show that the release of cysteine protease into the hemolymph ofB. morilarvae infected withfp25K-mutated BmNPVs is reduced and, as a consequence, postmortem host degradation of infected insects is lessened. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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20. Altered expression of testis-specific genes, piRNAs, and transposons in the silkworm ovary masculinized by a W chromosome mutation
- Author
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Hara Kahori, Fujii Tsuguru, Suzuki Yutaka, Sugano Sumio, Shimada Toru, Katsuma Susumu, and Kawaoka Shinpei
- Subjects
Biotechnology ,TP248.13-248.65 ,Genetics ,QH426-470 - Abstract
Abstract Background In the silkworm, Bombyx mori, femaleness is strongly controlled by the female-specific W chromosome. Originally, it was presumed that the W chromosome encodes female-determining gene(s), accordingly called Fem. However, to date, neither Fem nor any protein-coding gene has been identified from the W chromosome. Instead, the W chromosome is occupied with numerous transposon-related sequences. Interestingly, the silkworm W chromosome is a source of female-enriched PIWI-interacting RNAs (piRNAs). piRNAs are small RNAs of 23-30 nucleotides in length, which are required for controlling transposon activity in animal gonads. A recent study has identified a novel mutant silkworm line called KG, whose mutation in the W chromosome causes severe female masculinization. However, the molecular nature of KG line has not been well characterized yet. Results Here we molecularly characterize the KG line. Genomic PCR analyses using currently available W chromosome-specific PCR markers indicated that no large deletion existed in the KG W chromosome. Genetic analyses demonstrated that sib-crosses within the KG line suppressed masculinization. Masculinization reactivated when crossing KG females with wild type males. Importantly, the KG ovaries exhibited a significantly abnormal transcriptome. First, the KG ovaries misexpressed testis-specific genes. Second, a set of female-enriched piRNAs was downregulated in the KG ovaries. Third, several transposons were overexpressed in the KG ovaries. Conclusions Collectively, the mutation in the KG W chromosome causes broadly altered expression of testis-specific genes, piRNAs, and transposons. To our knowledge, this is the first study that describes a W chromosome mutant with such an intriguing phenotype.
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- 2012
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21. A case report and literature review: A 19-year-old with endometrial carcinoma treated with medroxyprogesterone acetate. Importance of the medical interview and endometrial examination.
- Author
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Katsuma S, Ariyoshi K, Nio A, Taguchi K, and Sonoda K
- Abstract
A 19-year-old woman had stage IA endometrial carcinoma treated with medroxyprogesterone acetate and experienced a recurrence. This patient's experience illustrates the importance of a thorough history and endometrial assessment in younger patients., Competing Interests: The authors declare no conflicts of interest., (© 2024 The Author(s). Clinical Case Reports published by John Wiley & Sons Ltd.)
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- 2024
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22. Codon Optimization-based Whole-gene Scanning Identifies Hidden Nucleotides Essential for Bombyx mori Nucleopolyhedrovirus polyhedrin Hyperexpression.
- Author
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Katsuma S and Matsuda-Imai N
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- Animals, Nucleotides genetics, Nucleotides metabolism, Promoter Regions, Genetic, Viral Structural Proteins genetics, Viral Structural Proteins metabolism, Codon genetics, Gene Expression Regulation, Viral, Cell Line, Nucleopolyhedroviruses genetics, Occlusion Body Matrix Proteins genetics, Bombyx virology, Bombyx genetics
- Abstract
During the late stage of infection, alphabaculoviruses produce many occlusion bodies (OBs) in the nuclei of the insect host's cells through the hyperexpression of polyhedrin (POLH), a major OB component encoded by polh. The strong polh promoter has been used to develop a baculovirus expression vector system for recombinant protein expression in cultured insect cells and larvae. However, the relationship between POLH accumulation and the polh coding sequence remains largely unelucidated. This study aimed to assess the importance of polh codon usage and/or nucleotide sequences in POLH accumulation by generating a baculovirus Bombyx mori nucleopolyhedrovirus (BmNPV) expressing mutant polh (co-polh) optimized according to the codon preference of its host insect. Although the deduced amino acid sequence of CO-POLH was the same as that of wild-type POLH, POLH accumulation was significantly lower in cells infected with the co-polh mutant. This reduction was due to decreased polh mRNA levels rather than translational repression. Analysis of mutant viruses with chimeric polh revealed that a 30 base-pair (bp) 5' proximal polh coding region was necessary for maintaining high polh mRNA levels. Sequence comparison of wild-type polh and co-polh identified five nucleotide differences in this region, indicating that these nucleotides were critical for polh hyperexpression. Furthermore, luciferase reporter assays showed that the 30 bp 5' coding region was sufficient for maintaining the polh promoter-driven high level of polh mRNA. Thus, our whole-gene scanning by codon optimization identified important hidden nucleotides for polh hyperexpression in alphabaculoviruses., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2024
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23. Expression of the Wolbachia male-killing factor Oscar impairs dosage compensation in lepidopteran embryos.
- Author
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Fukui T, Kiuchi T, Tomihara K, Muro T, Matsuda-Imai N, and Katsuma S
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- Animals, Male, Insect Proteins genetics, Insect Proteins metabolism, Gene Expression Profiling, Wolbachia genetics, Wolbachia metabolism, Moths genetics, Moths metabolism, Bombyx genetics, Bombyx metabolism
- Abstract
Wolbachia are intracellular bacteria in insects that can manipulate the sexual development and reproduction by male killing or other methods. We have recently identified a Wolbachia protein named Oscar that acts as a male-killing factor for lepidopteran insects. Oscar interacts with the Masculinizer (Masc) protein, which is required for both masculinization and dosage compensation (DC) in lepidopteran insects. Embryonic expression of Oscar inhibits masculinization and causes male killing in two lepidopteran species, Ostrinia furnacalis and Bombyx mori. However, it remains unknown whether Oscar-induced male killing is caused by a failure of DC. Here, we performed a transcriptome analysis of Oscar complementary RNA-injected O. furnacalis and B. mori embryos, and found that Oscar primarily targets the Masc protein, resulting in male killing by interfering with DC in lepidopteran insects., (© 2023 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.)
- Published
- 2024
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24. A seamless connection from the burst sequence to the start codon is essential for polyhedrin hyperexpression in alphabaculoviruses.
- Author
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Katsuma S and Matsuda-Imai N
- Subjects
- Animals, Codon, Initiator genetics, Viral Structural Proteins, Nucleopolyhedroviruses genetics, Bombyx genetics
- Abstract
Alphabaculoviruses produce a large number of occlusion bodies (OBs) in host cells during the late stage of infection. OBs are mainly composed of polyhedrin (POLH), and high-level transcription of the polh gene has been exploited to express foreign proteins in insect cells. While making Bombyx mori nucleopolyhedrovirus (BmNPV) polh mutants using a conventional transfer vector-based method, we noticed that a virus with a short sequence insertion just before the polh start codon produces fewer very small OBs. Detailed analysis of several BmNPV mutants revealed that insertions between the burst sequence and start codon markedly decrease POLH accumulation and polh transcription. We further confirmed this decrease using recombinant viruses expressing a reporter gene driven by the polh promoter. These findings underscore the critical importance of a seamless connection from the burst sequence to the start codon for baculovirus polh hyperexpression., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)
- Published
- 2023
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25. Two Complete Genomes of Male-Killing Wolbachia Infecting Ostrinia Moth Species Illuminate Their Evolutionary Dynamics and Association with Hosts.
- Author
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Muro T, Hikida H, Fujii T, Kiuchi T, and Katsuma S
- Subjects
- Animals, Male, Phylogeny, Sex Ratio, Genomics, Moths genetics, Wolbachia genetics
- Abstract
Wolbachia is an extremely widespread intracellular symbiont which causes reproductive manipulation on various arthropod hosts. Male progenies are killed in Wolbachia-infected lineages of the Japanese Ostrinia moth population. While the mechanism of male killing and the evolutionary interaction between host and symbiont are significant concerns for this system, the absence of Wolbachia genomic information has limited approaches to these issues. We determined the complete genome sequences of wFur and wSca, the male-killing Wolbachia of Ostrinia furnacalis and Ostrinia scapulalis. The two genomes shared an extremely high degree of homology, with over 95% of the predicted protein sequences being identical. A comparison of these two genomes revealed nearly minimal genome evolution, with a strong emphasis on the frequent genome rearrangements and the rapid evolution of ankyrin repeat-containing proteins. Additionally, we determined the mitochondrial genomes of both species' infected lineages and performed phylogenetic analyses to deduce the evolutionary dynamics of Wolbachia infection in the Ostrinia clade. According to the inferred phylogenetic relationship, two possible scenarios were proposed: (1) Wolbachia infection was established in the Ostrinia clade prior to the speciation of related species such as O. furnacalis and O. scapulalis, or (2) Wolbachia infection in these species was introgressively transferred from a currently unidentified relative. Simultaneously, the relatively high homology of mitochondrial genomes suggested recent Wolbachia introgression between infected Ostrinia species. The findings of this study collectively shed light on the host-symbiont interaction from an evolutionary standpoint., (© 2023. The Author(s).)
- Published
- 2023
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26. Non-gonadal somatic piRNA pathways ensure sexual differentiation, larval growth, and wing development in silkworms.
- Author
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Kiuchi T, Shoji K, Izumi N, Tomari Y, and Katsuma S
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- Animals, Larva genetics, Sex Differentiation, Piwi-Interacting RNA, Drosophila, Bombyx genetics
- Abstract
PIWI-interacting RNAs (piRNAs) guide PIWI proteins to target transposons in germline cells, thereby suppressing transposon activity to preserve genome integrity in metazoans' gonadal tissues. Piwi, one of three Drosophila PIWI proteins, is expressed in the nucleus and suppresses transposon activity by forming heterochromatin in an RNA cleavage-independent manner. Recently, Piwi was reported to control cell metabolism in Drosophila fat body, providing an example of piRNAs acting in non-gonadal somatic tissues. However, mutant flies of the other two PIWI proteins, Aubergine (Aub) and Argonaute3 (Ago3), show no apparent phenotype except for infertility, blurring the importance of the piRNA pathway in non-gonadal somatic tissues. The silkworm, Bombyx mori, possesses two PIWI proteins, Siwi (Aub homolog) and BmAgo3 (Ago3 homolog), whereas B. mori does not have a Piwi homolog. Siwi and BmAgo3 are mainly expressed in gonadal tissues and play a role in repressing transposon activity by cleaving transposon RNA in the cytoplasm. Here, we generated Siwi and BmAgo3 loss-of-function mutants of B. mori and found that they both showed delayed larval growth and failed to become adult moths. They also exhibited defects in wing development and sexual differentiation. Transcriptome analysis revealed that loss of somatic piRNA biogenesis pathways results in abnormal expression of not only transposons but also host genes, presumably causing severe growth defects. Our results highlight the roles of non-gonadal somatic piRNAs in B. mori development., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2023 Kiuchi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Published
- 2023
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27. A method for screening the suppressor genes of siRNA and piRNA pathways using cultured silkworm cells.
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Sugiyama H and Katsuma S
- Abstract
The BmN-4 cell line originates from the ovaries of silkworm, Bombyx mori , and possesses endogenous small interfering RNA (siRNA) and PIWI-interacting RNA (piRNA) pathways. BmN-4 cells are latently infected with Bombyx mori latent virus (BmLV), an RNA virus whose replication is strictly controlled by both siRNA and piRNA pathways. Knockdown or knockout of the core factors of these two small RNA pathways increases BmLV RNA amount, which in turn inhibits cell growth. Here, we used the known RNAi suppressor CrPV-1A to assess whether the BmN-4 cell line can be used for screening the suppressors of siRNA and piRNA pathways., Competing Interests: The authors declare that there are no conflicts of interest present., (Copyright: © 2023 by the authors.)
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- 2023
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28. Expression and localization of Bombyx mori nucleopolyhedrovirus GP37.
- Author
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Fujimoto S, Fujimaki K, Suzuki T, Katsuma S, and Iwanaga M
- Subjects
- Animals, Mitochondria, Nucleopolyhedroviruses genetics, Nucleopolyhedroviruses metabolism
- Abstract
Mitochondria play an essential role in intracellular energy metabolism. This study described the involvement of Bombyx mori nucleopolyhedrovirus (BmNPV) GP37 (BmGP37) in host mitochondria. Herein, the proteins associated with host mitochondria isolated from BmNPV-infected or mock-infected cells by two-dimensional gel electrophoresis were compared. One mitochondria-associated protein in virus-infected cells was identified as BmGP37 by liquid chromatography-mass spectrometry analysis. Furthermore, the BmGP37 antibodies were generated, which could react specifically with BmGP37 in the BmNPV-infected BmN cells. Western blot experiments showed that BmGP37 was expressed at 18 h post-infection and was verified as a mitochondria-associated protein. Immunofluorescence analysis demonstrated that BmGP37 localized to the host mitochondria during BmNPV infection. Furthermore, western blot analysis revealed that BmGP37 is a novel component protein of the occlusion-derived virus (ODV) of BmNPV. The present results indicated that BmGP37 is one of the ODV-associated proteins and may have important roles in host mitochondria during BmNPV infection., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
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- 2023
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29. Masculinizer is not post-transcriptionally regulated by female-specific piRNAs during sex determination in the Asian corn borer, Ostrinia furnacalis.
- Author
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Fukui T, Shoji K, Kiuchi T, Suzuki Y, and Katsuma S
- Subjects
- Female, Animals, Male, Piwi-Interacting RNA, Zea mays, Insect Proteins genetics, Insect Proteins metabolism, RNA, Messenger metabolism, RNA, Small Interfering genetics, Moths genetics, Moths metabolism, Bombyx metabolism
- Abstract
Lepidopteran insects are heterogametic in females, although most insect species are heterogametic in males. In a lepidopteran model species, the silkworm Bombyx mori (Bombycoidea), the uppermost sex determinant Feminizer (Fem) has been identified on the female-specific W chromosome. Fem is a precursor of PIWI-interacting small RNA (piRNA). Fem piRNA forms a complex with Siwi, one of the two B. mori PIWI-clade Argonaute proteins. In female embryos, Fem piRNA-Siwi complex cleaves the mRNA of the male-determining gene Masculinizer (Masc), directing the female-determining pathway. In male embryos, Masc activates the male-determining pathway in the absence of Fem piRNA. Recently, W chromosome-derived piRNAs complementary to Masc mRNA have also been identified in the diamondback moth Plutella xylostella (Yponomeutoidea), indicating the convergent evolution of piRNA-dependent sex determination in Lepidoptera. Here, we show that this is not the case in the Asian corn borer, Ostrinia furnacalis (Pyraloidea). Although our previous studies demonstrated that O. furnacalis Masc (OfMasc) has a masculinizing function in the embryonic stage, the expression level of OfMasc was indistinguishable between the sexes at the timing of sex determination. Deep sequencing analysis identified no female-specific small RNAs mapped onto OfMasc mRNA. Embryonic knockdown of two PIWI genes did not affect the expression level of OfMasc in either sex. These results demonstrated that piRNA-dependent reduction of Masc mRNA in female embryos is not a common strategy of sex determination, which suggests the possibility of divergent evolution of sex determinants across the order Lepidoptera., (Copyright © 2023 Elsevier Ltd. All rights reserved.)
- Published
- 2023
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30. Recessive embryonic lethal mutations uncovered in heterozygous condition in silkworm semiconsomic strains.
- Author
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Tomihara K, Tanaka S, Katsuma S, Shimada T, Kobayashi J, and Kiuchi T
- Subjects
- Animals, Mutation, Japan, Bombyx genetics, Bombyx metabolism
- Abstract
In this study, we found two embryonic lethal mutations, t04 lethal (l-t04) and m04 lethal (l-m04), in semiconsomic strains T04 and M04, respectively. In these semiconsomic strains, the entire diploid genome, except for one chromosome 4 of the wild silkworm Bombyx mandarina, is substituted with chromosomes of the domesticated silkworm B. mori, and l-t04 and l-m04 mutations are located on B. mandarina-derived chromosome 4. To clarify the cause of the lethalities and the genes responsible for these mutations, positional cloning and CRISPR/Cas9 mediated knockout screening were performed. Finally, genetic complementation tests identified the mutations responsible for the l-t04 and l-m04 as the Bombyx homolog of imaginal discs arrested (Bmida) and TATA box binding protein-associated factor 5 (BmTaf5), respectively. Lethal stages of each knockout mutant indicated the importance of these genes in B. mori late embryogenesis. The lethal mutations responsible for l-t04 and l-m04 were not found in parental strains or wild B. mandarina collected from 39 distinct locations in Japan, indicating that both mutations were independently introduced during or after the development of the semiconsomic strains. We conclude that the recessive embryonic lethality in the T04 and M04 strains is due to deleterious mutations produced in B. mandarina-derived chromosome 4., (Copyright © 2023 Elsevier Ltd. All rights reserved.)
- Published
- 2023
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31. The piRNA cluster torimochi is an expanding transposon in cultured silkworm cells.
- Author
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Shoji K, Umemura Y, Katsuma S, and Tomari Y
- Subjects
- Animals, Female, RNA, Small Interfering genetics, DNA Transposable Elements, Cells, Cultured, Argonaute Proteins genetics, Germ Cells metabolism, Piwi-Interacting RNA, Bombyx genetics
- Abstract
PIWI proteins and PIWI-interacting RNAs (piRNAs) play a central role in repressing transposable elements in animal germ cells. It is thought that piRNAs are mainly produced from discrete genomic loci named piRNA clusters, which often contain many "dead" transposon remnants from past invasions and have heterochromatic features. In the genome of silkworm ovary-derived cultured cells called BmN4, a well-established model for piRNA research, torimochi was previously annotated as a unique and specialized genomic region that can capture transgenes and produce new piRNAs bearing a trans-silencing activity. However, the sequence identity of torimochi has remained elusive. Here, we carefully characterized torimochi by utilizing the updated silkworm genome sequence and the long-read sequencer MinION. We found that torimochi is in fact a full-length gypsy-like LTR retrotransposon, which is exceptionally active and has massively expanded its copy number in BmN4 cells. Many copies of torimochi in BmN4 cells have features of open chromatin and the ability to produce piRNAs. Therefore, torimochi may represent a young, growing piRNA cluster, which is still "alive" and active in transposition yet capable of trapping other transposable elements to produce de novo piRNAs., Competing Interests: The authors declare that they have no conflict of interest., (Copyright: © 2023 Shoji et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
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- 2023
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32. A Wolbachia factor for male killing in lepidopteran insects.
- Author
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Katsuma S, Hirota K, Matsuda-Imai N, Fukui T, Muro T, Nishino K, Kosako H, Shoji K, Takanashi H, Fujii T, Arimura SI, and Kiuchi T
- Subjects
- Male, Animals, Dosage Compensation, Genetic, Insect Proteins genetics, Insect Proteins metabolism, Wolbachia metabolism, Bombyx genetics, Bombyx metabolism, Moths microbiology
- Abstract
Bacterial symbionts, such as Wolbachia species, can manipulate the sexual development and reproduction of their insect hosts. For example, Wolbachia infection induces male-specific death in the Asian corn borer Ostrinia furnacalis by targeting the host factor Masculinizer (Masc), an essential protein for masculinization and dosage compensation in lepidopteran insects. Here we identify a Wolbachia protein, designated Oscar, which interacts with Masc via its ankyrin repeats. Embryonic expression of Oscar inhibits Masc-induced masculinization and leads to male killing in two lepidopteran insects, O. furnacalis and the silkworm Bombyx mori. Our study identifies a mechanism by which Wolbachia induce male killing of host progeny., (© 2022. The Author(s).)
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- 2022
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33. The two Gtsf paralogs in silkworms orthogonally activate their partner PIWI proteins for target cleavage.
- Author
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Izumi N, Shoji K, Kiuchi T, Katsuma S, and Tomari Y
- Abstract
The PIWI-interacting RNA (piRNA) pathway is a protection mechanism against transposons in animal germ cells. Most PIWI proteins possess piRNA-guided endonuclease activity, which is critical for silencing transposons and producing new piRNAs. Gametocyte-specific factor 1 (Gtsf1), an evolutionarily conserved zinc finger protein, promotes catalysis by PIWI proteins. Many animals have multiple Gtsf1 paralogs; however, their respective roles in the piRNA pathway are not fully understood. Here, we dissected the roles of Gtsf1 and its paralog Gtsf1-like (Gtsf1L) in the silkworm piRNA pathway. We found that Gtsf1 and Gtsf1L preferentially bind the two silkworm PIWI paralogs, Siwi and BmAgo3, respectively, and facilitate the endonuclease activity of each PIWI protein. This orthogonal activation effect was further supported by specific reduction of BmAgo3-bound Masculinizer piRNA and Siwi-bound Feminizer piRNA, the unique piRNA pair required for silkworm feminization, upon depletion of Gtsf1 and Gtsf1L, respectively. Our results indicate that the two Gtsf paralogs in silkworms activate their respective PIWI partners, thereby facilitating the amplification of piRNAs., (Published by Cold Spring Harbor Laboratory Press for the RNA Society.)
- Published
- 2022
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34. Mutations in the polyhedrin NLS affect the assembly and polyhedral shape of alphabaculovirus occlusion bodies.
- Author
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Katsuma S
- Subjects
- Animals, Mutation, Nuclear Localization Signals genetics, Bombyx, Nucleopolyhedroviruses genetics
- Abstract
Alphabaculoviruses produce occlusion bodies (OBs) in the nucleus of the infected cells at the late stage of infection. OBs are mainly composed of a single viral protein called polyhedrin (POLH). Autographa californica multiple nucleopolyhedrovirus (AcMNPV) POLH possesses a monopartite nuclear localization signal sequence (NLS), KRKK, from 32nd to 35th residues. However, the functions of POLH NLS of other alphabaculoviruses remain unknown. Here, POLH NLS mutants of Bombyx mori nucleopolyhedrovirus (BmNPV) were generated and NLS function as well as the relationship between NLS and OB localization or morphology was investigated. Deletion or mutation of BmNPV POLH NLS severely affected POLH and OB intracellular localization. Additionally, viruses in which the arginine residue at the 33rd position of POLH was mutated produced a lower number of OBs, which was presumably due to decreased POLH accumulation in the infected cells. Furthermore, cytoplasmic OBs were morphologically aberrant, even though nuclear OB morphology was normal in the same cell. These results indicate that NLS is required for nuclear localization and efficient accumulation of BmNPV POLH, which heavily affect the number and morphology of OBs., Competing Interests: Declaration of competing interest The author declares that he has no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Published
- 2022
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35. Resistance mechanism of Nid-1, a dominant non-susceptibility gene, against Bombyx mori densovirus 1 infection.
- Author
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Ito K, Sivaprasad V, Katsuma S, Yokoyama T, and Kadono-Okuda K
- Subjects
- Animals, DNA, Viral metabolism, Bombyx, Densovirus genetics, Insect Viruses genetics
- Abstract
Bombyx mori densovirus 1 (BmDV1) is a pathogen that causes flacherie disease in mulberry silkworms (B. mori). The absolute resistance (non-susceptibility) to BmDV1 of certain silkworm strains is determined independently by two genes, nsd-1 and Nid-1. Previously, we investigated the expression of viral transcript in virus-inoculated silkworms carrying different nsd-1 and Nid-1 genotypes, and observed that nsd-1 and Nid-1 expression blocked the early and late steps of BmDV1 infection, respectively. In addition, we found that nsd-1 encoded a Bombyx-specific mucin-like membrane protein only present on the surface of the midgut, where BmDV1 could infect. In this study, we dissected the resistance mechanism by Nid-1 against BmDV1 infection by investigating the sequential changes in the accumulation of viral DNA, transcripts, and proteins derived from BmDV1 in susceptible strain (pxj) and Nid-1-carrying resistant strain (No. 908) after inoculation with BmDV1. Genomic PCR results showed that the BmDV1 DNA was detected immediately after the infection in both strains but rapidly decreased in the Nid-1-carrying strain No. 908 compared with the susceptible strain pxj. RT-PCR results also showed that the BmDV1 transcripts of Nid-1-carrying strain No. 908 were rapidly decreased after the infection. Moreover, BmDV1-derived proteins were not detected in No. 908 throughout the infection. These results suggest that Nid-1 expression might inhibit the accumulation of viral DNA and transcripts. As Nid-1 has not been molecularly characterized, its identification will contribute to the elucidation of the interactions between the silkworm and BmDV1., (Copyright © 2022 Elsevier B.V. All rights reserved.)
- Published
- 2022
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36. Masculinizer-induced dosage compensation is achieved by transcriptional downregulation of both copies of Z-linked genes in the silkworm, Bombyx mori .
- Author
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Tomihara K, Kawamoto M, Suzuki Y, Katsuma S, and Kiuchi T
- Subjects
- Animals, Dosage Compensation, Genetic, Down-Regulation, Female, Insect Proteins genetics, Insect Proteins metabolism, Male, Sex Chromosomes genetics, Sex Chromosomes metabolism, Bombyx genetics, Bombyx metabolism
- Abstract
The evolution of dosage compensation produces similar expression of sex-linked and autosomal genes in the heterogametic sex. The silkworm ( Bombyx mori ), a lepidopteran insect, has a female heterogametic WZ sex determination system. A Z-linked gene, Masculinizer ( Masc ), is the primary determinant of maleness and dosage compensation in B. mori . However, it remains unknown whether one of the two Z chromosomes is inactivated or both Z chromosomes are suppressed in B. mori males. Hence, we performed transcriptome analysis using hybrids between two B. mori strains and analysed allele-specific expression to distinguish these alternatives. Our analysis revealed that genes on both the maternal and paternal Z chromosomes are transcriptionally upregulated in Masc knocked down males. We therefore conclude that both Z chromosomes are transcriptionally downregulated in B. mori males, similar to the system in Caenorhabditis elegans .
- Published
- 2022
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37. Transcriptome analysis in the silkworm Bombyx mori overexpressing piRNA-resistant Masculinizer gene.
- Author
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Tomihara K, Katsuma S, and Kiuchi T
- Subjects
- Animals, Female, Gene Expression Profiling, Humans, Infant, Newborn, Insect Proteins genetics, Insect Proteins metabolism, Male, RNA, Messenger genetics, RNA, Small Interfering genetics, Bombyx metabolism
- Abstract
Dosage compensation is a process that produces a similar expression of sex-linked and autosomal genes. In the silkworm Bombyx mori with a WZ sex-determination system, the expression from the single Z in WZ females matches that of ZZ males due to the suppression of Z-linked genes in males. A primary maleness determinant gene, Masculinizer (Masc), is also required for dosage compensation. In females, silkworm Piwi is complexed with the W chromosome-derived female-specific Feminizer (Fem) PIWI-interacting RNA (piRNA) and cleaves Masc mRNA. When Fem piRNA-resistant Masc cDNA (Masc-R) is overexpressed in both sexes, only female larvae are dead during the larval stage. In this study, transcriptome analysis was performed in neonate larvae to examine the effects of Masc-R overexpression on a global gene expression profile. Z-linked genes were globally repressed in Masc-R-overexpressing females due to force-driven dosage compensation. In contrast, Masc-R overexpression had little effect on the expression of Z-linked genes and the male-specific isoform of B. mori insulin-like growth factor II mRNA-binding protein in males, indicating that excessive Masc expression strengthens neither dosage compensation nor maleness in males. Fourteen genes were differentially expressed between Masc-R-overexpressing and control neonate larvae in both sexes, suggesting Masc functions other than dosage compensation and masculinization., Competing Interests: Declaration of interests The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Published
- 2022
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38. SilkBase: an integrated transcriptomic and genomic database for Bombyx mori and related species.
- Author
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Kawamoto M, Kiuchi T, and Katsuma S
- Subjects
- Animals, Databases, Nucleic Acid, Expressed Sequence Tags, Genome, Genomics, Silk, Transcriptome genetics, Bombyx genetics
- Abstract
We introduce SilkBase as an integrated database for transcriptomic and genomic resources of the domesticated silkworm Bombyx mori and related species. SilkBase is the oldest B. mori database that was originally established as the expressed sequence tag database since 1999. Here, we upgraded the database by including the datasets of the newly assembled B. mori complete genome sequence, predicted gene models, bacterial artificial chromosome (BAC)-end and fosmid-end sequences, complementary DNA (cDNA) reads from 69 libraries, RNA-seq data from 10 libraries, PIWI-interacting RNAs (piRNAs) from 13 libraries, ChIP-seq data of 9 histone modifications and HP1 proteins and transcriptome and/or genome data of four B. mori-related species, i.e. Bombyx mandarina, Trilocha varians, Ernolatia moorei and Samia ricini. Our new integrated genome browser easily provides a snapshot of tissue- and stage-specific gene expression, alternative splicing, production of piRNAs and histone modifications at the gene locus of interest. Moreover, SilkBase is useful for performing comparative studies among five closely related lepidopteran insects. Database URL: https://silkbase.ab.a.u-tokyo.ac.jp., (© The Author(s) 2022. Published by Oxford University Press.)
- Published
- 2022
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39. Functional Characterization of Silkworm PIWI Proteins by Embryonic RNAi.
- Author
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Kiuchi T and Katsuma S
- Subjects
- Animals, Female, Insect Proteins genetics, RNA Interference, RNA, Small Interfering genetics, Sex Chromosomes, Bombyx genetics
- Abstract
The molecular mechanisms of sex-determination systems among insect orders and species are diverse. Therefore, genes involved in sex determination are strong candidates for insect pest management. Even though lepidopterans are major agricultural insect pests that cause widespread economic damage to various crops, their sex-determination systems have not been fully elucidated, even in the silkworm (Bombyx mori), a model lepidopteran insect. In 2014, we found that a female-specific W chromosome-derived PIWI-interacting RNA (piRNA) determines femaleness in silkworms. To analyze the function of two core silkworm piRNA biogenesis pathway genes, Siwi and BmAgo3, in the sex-determination system, we developed a genomic DNA and total RNA extraction strategy for a siRNA-injected single embryo. The siRNA-injected embryo can be molecularly sexed by W chromosome-specific DNA markers. Using complementary DNA (cDNA) reverse transcribed from the sexed RNA, we evaluated the knockdown effect of the PIWI protein-coding genes on a sexual development-related gene, Bombyx mori doublesex., (© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)
- Published
- 2022
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40. Mutations in a β-group of solute carrier gene are responsible for egg and eye coloration of the brown egg 4 (b-4) mutant in the silkworm, Bombyx mori.
- Author
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Tomihara K, Satta K, Matsuzaki S, Yoshitake K, Yamamoto K, Uchiyama H, Yajima S, Futahashi R, Katsuma S, Osanai-Futahashi M, and Kiuchi T
- Subjects
- Amino Acid Sequence, Animals, Base Sequence, Bombyx growth & development, Bombyx metabolism, Insect Proteins chemistry, Insect Proteins metabolism, Larva growth & development, Larva metabolism, Mutation, Ovum chemistry, Phylogeny, Pigmentation genetics, Pigments, Biological analysis, Sequence Alignment, Bombyx genetics, Compound Eye, Arthropod chemistry, Insect Proteins genetics
- Abstract
The brown egg 4 (b-4) is a recessive mutant in the silkworm (Bombyx mori), whose egg and adult compound eyes exhibit a reddish-brown color instead of normal purple and black, respectively. By double digest restriction-site associated DNA sequencing (ddRAD-seq) analysis, we narrowed down a region linked to the b-4 phenotype to approximately 1.1 Mb that contains 69 predicted gene models. RNA-seq analysis in a b-4 strain indicated that one of the candidate genes had a different transcription start site, which generates a short open reading frame. We also found that exon skipping was induced in the same gene due to an insertion of a transposable element in other two b-4 mutant strains. This gene encoded a putative amino acid transporter that belongs to the β-group of solute carrier (SLC) family and is orthologous to Drosophila eye color mutant gene, mahogany (mah). Accordingly, we named this gene Bmmah. We performed CRISPR/Cas9-mediated gene knockout targeting Bmmah. Several adult moths in generation 0 (G
0 ) had totally or partially reddish-brown compound eyes. We also established three Bmmah knockout strains, all of which exhibit reddish-brown eggs and adult compound eyes. Furthermore, eggs from complementation crosses between the b-4 mutants and the Bmmah knockout mutants also exhibited reddish-brown color, which was similar to the b-4 mutant eggs, indicating that Bmmah is responsible for the b-4 phenotypes., (Copyright © 2021. Published by Elsevier Ltd.)- Published
- 2021
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41. H3K4me3 histone modification in baculovirus-infected silkworm cells.
- Author
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Shoji K, Kokusho R, Kawamoto M, Suzuki Y, and Katsuma S
- Subjects
- Animals, Baculoviridae genetics, Baculoviridae pathogenicity, Bombyx virology, Chromatin virology, Gene Expression Regulation genetics, High-Throughput Nucleotide Sequencing, Histone Code genetics, Nucleopolyhedroviruses pathogenicity, Protein Processing, Post-Translational genetics, Bombyx genetics, Chromatin genetics, Histones genetics, Nucleopolyhedroviruses genetics
- Abstract
Baculovirus infection modulates the chromatin states and gene expression of host insect cells. Here we performed chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) of H3 trimethylated at Lys4 (H3K4me3) histone modification in Bombyx mori nucleopolyhedrovirus-infected Bombyx mori cells. The ChIP-seq data revealed the changes of the genome-wide distribution and accumulation of euchromatic histone marks in host insect cells during the progression of baculovirus infection., (© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Published
- 2021
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42. RNase κ promotes robust piRNA production by generating 2',3'-cyclic phosphate-containing precursors.
- Author
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Shigematsu M, Kawamura T, Morichika K, Izumi N, Kiuchi T, Honda S, Pliatsika V, Matsubara R, Rigoutsos I, Katsuma S, Tomari Y, and Kirino Y
- Subjects
- Animals, Base Sequence, Bombyx, Cell Line, Endoribonucleases metabolism, Female, Insect Proteins metabolism, Male, Mice, Inbred C57BL, Mutation, Phosphatidic Acids chemistry, RNA chemistry, RNA metabolism, RNA Interference, RNA, Small Interfering metabolism, RNA-Seq methods, Testis metabolism, Mice, Endoribonucleases genetics, Gene Expression Profiling methods, Insect Proteins genetics, RNA genetics, RNA, Small Interfering genetics
- Abstract
In animal germlines, PIWI proteins and the associated PIWI-interacting RNAs (piRNAs) protect genome integrity by silencing transposons. Here we report the extensive sequence and quantitative correlations between 2',3'-cyclic phosphate-containing RNAs (cP-RNAs), identified using cP-RNA-seq, and piRNAs in the Bombyx germ cell line and mouse testes. The cP-RNAs containing 5'-phosphate (P-cP-RNAs) identified by P-cP-RNA-seq harbor highly consistent 5'-end positions as the piRNAs and are loaded onto PIWI protein, suggesting their direct utilization as piRNA precursors. We identified Bombyx RNase Kappa (BmRNase κ) as a mitochondria-associated endoribonuclease which produces cP-RNAs during piRNA biogenesis. BmRNase κ-depletion elevated transposon levels and disrupted a piRNA-mediated sex determination in Bombyx embryos, indicating the crucial roles of BmRNase κ in piRNA biogenesis and embryonic development. Our results reveal a BmRNase κ-engaged piRNA biogenesis pathway, in which the generation of cP-RNAs promotes robust piRNA production., (© 2021. The Author(s).)
- Published
- 2021
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43. Loss of p24 from the Bombyx mori nucleopolyhedrovirus genome results in the formation of cuboidal occlusion bodies.
- Author
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Kokusho R and Katsuma S
- Subjects
- Amino Acid Substitution, Animals, Bombyx virology, Larva virology, Mutation, Nucleopolyhedroviruses pathogenicity, Genome, Viral, Nucleopolyhedroviruses genetics, Nucleopolyhedroviruses physiology, Occlusion Bodies, Viral genetics, Occlusion Bodies, Viral physiology, Viral Proteins genetics
- Abstract
Some insect viruses produce the occlusion body (OB), a large crystalline particle comprising a viral protein that occludes virions to protect them from harsh environments. The shapes and sizes of OBs are diverse depending on baculovirus species, but the detailed molecular mechanism determining them has yet to be totally clarified yet. Here we generated Bombyx mori nucleopolyhedrovirus (BmNPV) mutants of the p24 gene that encodes a viral capsid protein and found that p24-mutated BmNPVs produced cuboidal OBs with a slightly larger size than typical truncated octahedral OBs produced by wild-type BmNPVs. Meanwhile, p24 disruption has no significant impact on progeny virus production and viral pathogenicity. In addition, we experimentally demonstrated that a single amino acid substitution found in the P24 protein of the BmNPV Cubic isolate caused cuboidal OB production. These results suggest that p24 has a crucial role in generating the typical shape of OBs., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2021
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44. Bombyx mori nucleopolyhedrovirus ptp and egt genes are dispensable for triggering enhanced locomotory activity and climbing behavior in Bombyx mandarina larvae.
- Author
-
Kokusho R and Katsuma S
- Subjects
- Animals, Bombyx growth & development, Bombyx virology, Larva growth & development, Larva physiology, Larva virology, Locomotion, Bombyx physiology, Nucleopolyhedroviruses genetics
- Abstract
Baculoviruses are classic pathogens that alter host behavior to enhance their dispersal and transmission. While viral protein tyrosine phosphatase (ptp) has been considered as a critical factor for inducing enhanced locomotory activity, preceding investigations have reported that viral ecdysteroid UDP-glucosyltransferase (egt) contributes to triggering climbing behavior in some virus and host species. Here we found that both egt and ptp were dispensable for these abnormal behaviors in Bombyx mandarina larvae induced by Bombyx mori nucleopolyhedrovirus, thus implying that there is an unknown core mechanism of baculovirus-induced alteration of host behaviors., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2021
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45. Horizontal Gene Transfer and Gene Duplication of β-Fructofuranosidase Confer Lepidopteran Insects Metabolic Benefits.
- Author
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Dai X, Kiuchi T, Zhou Y, Jia S, Xu Y, Katsuma S, Shimada T, and Wang H
- Subjects
- Animals, Female, Homeostasis, Larva growth & development, Larva metabolism, Lepidoptera enzymology, Male, Sucrase metabolism, Biological Evolution, Gene Duplication, Gene Transfer, Horizontal, Lepidoptera genetics, beta-Fructofuranosidase genetics
- Abstract
Horizontal gene transfer (HGT) is a potentially critical source of material for ecological adaptation and the evolution of novel genetic traits. However, reports on posttransfer duplication in organism genomes are lacking, and the evolutionary advantages conferred on the recipient are generally poorly understood. Sucrase plays an important role in insect physiological growth and development. Here, we performed a comprehensive analysis of the evolution of insect β-fructofuranosidase transferred from bacteria via HGT. We found that posttransfer duplications of β-fructofuranosidase were widespread in Lepidoptera and sporadic occurrences of β-fructofuranosidase were found in Coleoptera and Hymenoptera. β-fructofuranosidase genes often undergo modifications, such as gene duplication, differential gene loss, and changes in mutation rates. Lepidopteran β-fructofuranosidase gene (SUC) clusters showed marked divergence in gene expression patterns and enzymatic properties in Bombyx mori (moth) and Papilio xuthus (butterfly). We generated SUC1 mutations in B. mori using CRISPR/Cas9 to thoroughly examine the physiological function of SUC. BmSUC1 mutant larvae were viable but displayed delayed growth and reduced sucrase activities that included susceptibility to the sugar mimic alkaloid found in high concentrations in mulberry. BmSUC1 served as a critical sucrase and supported metabolic homeostasis in the larval midgut and silk gland, suggesting that gene transfer of β-fructofuranosidase enhanced the digestive and metabolic adaptation of lepidopteran insects. These findings highlight not only the universal function of β-fructofuranosidase with a link to the maintenance of carbohydrate metabolism but also an underexplored function in the silk gland. This study expands our knowledge of posttransfer duplication and subsequent functional diversification in the adaptive evolution and lineage-specific adaptation of organisms., (© The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.)
- Published
- 2021
- Full Text
- View/download PDF
46. High-resolution analysis of baculovirus-induced host manipulation in the domestic silkworm, Bombyx mori - CORRIGENDUM.
- Author
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Hikida H and Katsuma S
- Published
- 2021
- Full Text
- View/download PDF
47. Characterization of nuclear localization signal in Ostrinia furnacalis Masculinizer protein.
- Author
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Hirota K, Matsuda-Imai N, Kiuchi T, and Katsuma S
- Subjects
- Animals, Bombyx genetics, Cell Line, Insect Proteins genetics, Insect Proteins metabolism, Insecta, Moths genetics, Nuclear Localization Signals genetics, Nuclear Localization Signals metabolism
- Abstract
Bombyx mori Masculinizer protein (BmMasc) is essential for both masculinization and dosage compensation in B. mori. We previously identified a bipartite nuclear localization signal (NLS) of BmMasc and two essential residues (lysine at 274 [K274] and arginine at 275 [R275]) implicated in its function. Sequence comparison showed the presence of putative NLSs in lepidopteran Masc proteins, but their functional properties and critical residues are unknown. Here we characterized a putative NLS of Ostrinia furnacalis Masc (OfMasc) using B. mori ovary-derived BmN-4 cell line. Deletion and alanine scanning mutagenesis revealed that a putative NLS is required for nuclear localization of OfMasc. However, mutations at both K227 and R228, which correspond to K274 and R275 of BmMasc, respectively, do not greatly abolish the NLS activity. Additional mutagenesis analysis revealed that triple mutations at K227, R228, and K240 almost completely inhibited OfMasc nuclear localization. These results suggest that lepidopteran Masc proteins possess a common functional NLS, but the critical residues for its activity are different. Moreover, we examined the masculinizing activity of OfMasc derivatives and found that nuclear localization is not required for the masculinizing activity of OfMasc. The results from our studies indicate that lepidopteran Masc proteins function in the cytoplasm to drive masculinizing cascade., (© 2021 Wiley Periodicals LLC.)
- Published
- 2021
- Full Text
- View/download PDF
48. CRISPR/Cas9-mediated mutagenesis of Ago2 and Siwi in silkworm cultured cells.
- Author
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Katsuma S, Shoji K, Suzuki Y, and Kiuchi T
- Subjects
- Animals, Bombyx genetics, CRISPR-Cas Systems, Cell Proliferation, Cells, Cultured, Gene Editing, Insect Proteins genetics, Loss of Function Mutation, RNA, Small Interfering genetics, RNA, Viral genetics, Signal Transduction, Argonaute Proteins genetics, Bombyx cytology, Mutagenesis, Site-Directed methods, Tymoviridae genetics
- Abstract
The BmN-4 cell line, originated from the silkworm Bombyx mori ovary, possesses endogenous small interfering RNA (siRNA) and PIWI-interacting RNA (piRNA) pathways. We performed CRISPR/Cas9-mediated genome editing of Ago2 and Siwi, which are the core factors for siRNA and piRNA pathways, respectively, to understand the importance of the two distinct small RNA pathways in this cell line. We found that approximately half of the alleles contained loss-of-function mutations in both Ago2- and Siwi-mutated cells. The mutated cells grew at a slower rate compared to the control cells, strongly suggesting that the siRNA and piRNA pathways are both crucial for the normal growth of BmN-4 cells. The amounts of piRNAs decreased markedly in the Siwi-mutated cells, but global de-repression of transposable elements was not observed. Although the RNA amount of latently infected RNA virus, Bombyx mori macula-like virus (BmLV), increased in both Ago2- and Siwi-mutated cells, the siRNA and piRNA pathways showed a bias toward targeting BmLV genomic and subgenomic RNA, respectively. These results indicate the common, specific, and crucial roles of the two small RNA pathways in B. mori cultured cells., (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Published
- 2021
- Full Text
- View/download PDF
49. Potential for small RNA production against Bombyx mori latent virus in Bombyx mori ovaries.
- Author
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Katsuma S, Shoji K, Suzuki Y, and Iwanaga M
- Subjects
- Animals, Bombyx growth & development, Bombyx virology, Female, Larva growth & development, Larva immunology, Larva virology, Ovary immunology, Ovary metabolism, Bombyx immunology, Host-Pathogen Interactions immunology, Immunity, Innate, RNA, Small Interfering metabolism, Tymoviridae physiology
- Abstract
Bombyx mori latent virus (BmLV) is a positive, single-stranded insect RNA virus closely related to plant maculaviruses. BmLV was first isolated from Bombyx mori ovary-derived cell line BmN-4, and this virus has already infected most B. mori-derived cultured cell lines. We previously reported that small interfering RNA (siRNA) and PIWI-interacting RNA (piRNA) pathways function cooperatively to maintain the amount of BmLV RNA for normal BmN-4 cell growth. On the other hand, BmLV does not propagate in B. mori larvae. Here we conducted BmLV injection into the larval body cavities of B. mori, and examined BmLV accumulation in larval ovaries where siRNA and piRNA pathways are both active, to investigate whether this in vivo resistance is governed by small RNA pathways. Expression levels of RNA-dependent RNA polymerase, coat protein, and p15 genes in BmLV-injected larval ovaries were extremely low compared with those in B. mori cultured cells, indicating that B. mori larval ovaries are more resistant to BmLV than B. mori cultured cells. We also sequenced small RNAs prepared from BmLV-injected larval ovaries and mapped them onto the BmLV genome. Although their amounts were very small, we were able to detect BmLV-derived small RNAs in the ovaries. According to their length distribution and nucleotide bias, they were likely to be siRNAs and piRNAs. These results suggest that B. mori ovaries can potentially produce small RNAs against BmLV, but the resistance of larval ovaries against BmLV is not dependent on RNA silencing pathways., (© 2020 Wiley Periodicals LLC.)
- Published
- 2021
- Full Text
- View/download PDF
50. Formation of the CenH3-Deficient Holocentromere in Lepidoptera Avoids Active Chromatin.
- Author
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Senaratne AP, Muller H, Fryer KA, Kawamoto M, Katsuma S, and Drinnenberg IA
- Subjects
- Animals, Bombyx metabolism, Cell Line, Centromere genetics, Centromere Protein A genetics, Chromosome Segregation, Insect Proteins genetics, Kinetochores metabolism, Bombyx genetics, Centromere metabolism, Centromere Protein A deficiency, Chromatin metabolism, Insect Proteins deficiency
- Abstract
Despite the essentiality for faithful chromosome segregation, centromere architectures are diverse among eukaryotes
1 , 2 and embody two main configurations: mono- and holocentromeres, referring, respectively, to localized or unrestricted distribution of centromeric activity. Of the two, some holocentromeres offer the curious condition of having arisen independently in multiple insects, most of which have lost the otherwise essential centromere-specifying factor CenH33 (first described as CENP-A in humans).4-7 The loss of CenH3 raises intuitive questions about how holocentromeres are organized and regulated in CenH3-lacking insects. Here, we report the first chromatin-level description of CenH3-deficient holocentromeres by leveraging recently identified centromere components6 , 7 and genomics approaches to map and characterize the holocentromeres of the silk moth Bombyx mori, a representative lepidopteran insect lacking CenH3. This uncovered a robust correlation between the distribution of centromere sites and regions of low chromatin activity along B. mori chromosomes. Transcriptional perturbation experiments recapitulated the exclusion of B. mori centromeres from active chromatin. Based on reciprocal centromere occupancy patterns observed along differentially expressed orthologous genes of Lepidoptera, we further found that holocentromere formation in a manner that is recessive to chromatin dynamics is evolutionarily conserved. Our results help us discuss the plasticity of centromeres in the context of a role for the chromosome-wide chromatin landscape in conferring centromere identity rather than the presence of CenH3. Given the co-occurrence of CenH3 loss and holocentricity in insects,7 we further propose that the evolutionary establishment of holocentromeres in insects was facilitated through the loss of a CenH3-specified centromere., Competing Interests: Declaration of Interests The authors declare no competing interests., (Copyright © 2020 Elsevier Inc. All rights reserved.)- Published
- 2021
- Full Text
- View/download PDF
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