Search

Introduction: Chieh-qua (Benincasa hispida Cogn. var. Chieh-qua How) is a wax gourd variety that is generally susceptible to infection and damage by Fusarium oxysporum during its cultivation. Therefore, analyzing the adaption mechanism of chieh-qua to F. Oxysporum infection is of great significance for cultivating resistant varieties. Methods: Through comparative transcriptome analysis, comparative metabolome analysis, integrated analysis of transcriptome and metabolome and between F. Oxysporum infected samples and control samples of susceptible lines Results: This study found that proteins such as NPR1, TGA and PR1 in plant hormone signal transduction pathway were up-regulated after infection, which may activate a series of plant secondary metabolic synthesis pathways. In addition, the expression of 27 genes in the flavonoid biosynthetic process in resistant lines after infection was significantly higher than that in susceptible lines, indicating that these genes may be involved in fungal resistance. This study also found that alternative splicing of genes may play an important role in responding to F. Oxysporum infection. For example, plant protein kinase genes such as EDR1, SRK2E and KIPK1 were not differentially expressed after F. Oxysporum infection, but the transcripts they produced differ at the transcription level. Finally, through comparative metabolome analysis, this study identified potentially functional substances such as oxalic acid that increased in content after F. Oxysporum infection. Through integrated analysis of transcriptome and metabolome, some differential expressed genes significantly related to differential metabolites were also identified. Discussion: This study provides a basis for understanding and utilizing chieh-qua's infection mechanism of F. Oxysporum through analysis of the transcriptome and metabolome. [ABSTRACT FROM AUTHOR]

Introduction: Flesh color is an essential trait in chieh-qua (Benincasa hispida Cogn. var. Chieh-qua How); however, the inheritance and molecular basis of green flesh trait remain unclear. Methods: In the present study, two F2 populations, derived from 1742 (white flesh) × FJ3211 (green flesh) and J16 (white flesh) × FJ5 (green flesh), were used to identify the green flesh (Cqgf) locus. Results: Genetic analysis revealed that the presence of green flesh was a quantitative trait that closely followed a normal distribution. Combining the results from QTL mapping and BSA-seq analysis, the Cqgf locus was preliminarily determined to be located on chromosome 05 and was narrowed down to a 2.55-Mb interval by linkage analysis. A large J16 × FJ5 F2 population comprising 3,180 individuals was subsequently used to screen the recombinants, and the Cqgf locus was fine-mapped to a region of 329.70 kb that harbors six genes. One of the candidate genes, Bch05G003700 , the zinc-finger transcription factor LOL1 (lsd one like 1 protein; CqLOL1), was the strongest candidate gene for the Cqgf locus according to sequence variation and expression analysis. Additionally, a point mutation (A > C) in CqLOL1 resulted in the substitution of threonine (T) with proline (P) in the amino acid sequence, showing a complete relationship linked with flesh color in a panel of 45 germplasms. Discussion: The study suggests that CqLOL1 promotes the accumulation of chlorophyll content in chieh-qua and lead to green flesh. Our findings establish a theoretical and technical foundation for breeding different flesh color lines and elucidating the underlying mechanisms of flesh color in chieh-qua. [ABSTRACT FROM AUTHOR]

IntroductionChieh-qua (Benincasa hispida Cogn. var. Chieh-qua How) is a wax gourd variety that is generally susceptible to infection and damage by Fusarium oxysporum during its cultivation. Therefore, analyzing the adaption mechanism of chieh-qua to F. Oxysporum infection is of great significance for cultivating resistant varieties.MethodsThrough comparative transcriptome analysis, comparative metabolome analysis, integrated analysis of transcriptome and metabolome and between F. Oxysporum infected samples and control samples of susceptible linesResultsThis study found that proteins such as NPR1, TGA and PR1 in plant hormone signal transduction pathway were up-regulated after infection, which may activate a series of plant secondary metabolic synthesis pathways. In addition, the expression of 27 genes in the flavonoid biosynthetic process in resistant lines after infection was significantly higher than that in susceptible lines, indicating that these genes may be involved in fungal resistance. This study also found that alternative splicing of genes may play an important role in responding to F. Oxysporum infection. For example, plant protein kinase genes such as EDR1, SRK2E and KIPK1 were not differentially expressed after F. Oxysporum infection, but the transcripts they produced differ at the transcription level. Finally, through comparative metabolome analysis, this study identified potentially functional substances such as oxalic acid that increased in content after F. Oxysporum infection. Through integrated analysis of transcriptome and metabolome, some differential expressed genes significantly related to differential metabolites were also identified.DiscussionThis study provides a basis for understanding and utilizing chieh-qua’s infection mechanism of F. Oxysporum through analysis of the transcriptome and metabolome.

IntroductionFlesh color is an essential trait in chieh-qua (Benincasa hispida Cogn. var. Chieh-qua How); however, the inheritance and molecular basis of green flesh trait remain unclear.MethodsIn the present study, two F2 populations, derived from 1742 (white flesh) × FJ3211 (green flesh) and J16 (white flesh) × FJ5 (green flesh), were used to identify the green flesh (Cqgf) locus.ResultsGenetic analysis revealed that the presence of green flesh was a quantitative trait that closely followed a normal distribution. Combining the results from QTL mapping and BSA-seq analysis, the Cqgf locus was preliminarily determined to be located on chromosome 05 and was narrowed down to a 2.55-Mb interval by linkage analysis. A large J16 × FJ5 F2 population comprising 3,180 individuals was subsequently used to screen the recombinants, and the Cqgf locus was fine-mapped to a region of 329.70 kb that harbors six genes. One of the candidate genes, Bch05G003700, the zinc-finger transcription factor LOL1 (lsd one like 1 protein; CqLOL1), was the strongest candidate gene for the Cqgf locus according to sequence variation and expression analysis. Additionally, a point mutation (A > C) in CqLOL1 resulted in the substitution of threonine (T) with proline (P) in the amino acid sequence, showing a complete relationship linked with flesh color in a panel of 45 germplasms.DiscussionThe study suggests that CqLOL1 promotes the accumulation of chlorophyll content in chieh-qua and lead to green flesh. Our findings establish a theoretical and technical foundation for breeding different flesh color lines and elucidating the underlying mechanisms of flesh color in chieh-qua.

Gynoecy demonstrates an earlier production of hybrids and a higher yield and improves the efficiency of hybrid seed production. Therefore, the utilization of gynoecy is beneficial for the genetic breeding of chieh-qua. However, little knowledge of gynoecious-related genes in chieh-qua has been reported until now. Here, we used an F2 population from the cross between the gynoecious line 'A36' and the monoecious line 'SX' for genetic mapping and revealed that chieh-qua gynoecy was regulated by a single recessive gene. We fine-mapped it into a 530-kb region flanked by the markers Indel-3 and KASP145 on Chr.8, which harbors eight candidate genes. One of the candidate genes, Bhi08G000345, encoding networked protein 4 (CqNET4), contained a nonsynonymous SNP resulting in the amino acid substitution of isoleucine (ATA; I) to methionine (ATG; M). CqNET4 was prominently expressed in the female flower, and only three genes related to ethylene synthesis were significantly expressed between 'A36' and 'SX.' The results presented here provide support for the CqNET4 as the most likely candidate gene for chieh-qua gynoecy, which differed from the reported gynoecious genes. [ABSTRACT FROM AUTHOR]

Gynoecy demonstrates an earlier production of hybrids and a higher yield and improves the efficiency of hybrid seed production. Therefore, the utilization of gynoecy is beneficial for the genetic breeding of chieh-qua. However, little knowledge of gynoecious-related genes in chieh-qua has been reported until now. Here, we used an F 2 population from the cross between the gynoecious line 'A36' and the monoecious line 'SX' for genetic mapping and revealed that chieh-qua gynoecy was regulated by a single recessive gene. We fine-mapped it into a 530-kb region flanked by the markers Indel-3 and KASP145 on Chr.8, which harbors eight candidate genes. One of the candidate genes, Bhi08G000345 , encoding networked protein 4 ( CqNET4 ), contained a non-synonymous SNP resulting in the amino acid substitution of isoleucine (ATA; I) to methionine (ATG; M). CqNET4 was prominently expressed in the female flower, and only three genes related to ethylene synthesis were significantly expressed between 'A36' and 'SX.' The results presented here provide support for the CqNET4 as the most likely candidate gene for chieh-qua gynoecy, which differed from the reported gynoecious genes., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Wang, Yang, Liu, Cao, Chen, Liu, Xie, Yan, Jiang and Peng.)