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Molecular characterization and functional analyses of a diapause hormone receptor-like gene in parthenogenetic Artemia.
- Source :
-
Peptides [Peptides] 2017 Apr; Vol. 90, pp. 100-110. Date of Electronic Publication: 2017 Feb 04. - Publication Year :
- 2017
-
Abstract
- In arthropods, mature females under certain conditions produce and release encysted gastrula embryos that enter diapause, a state of obligate dormancy. The process is presumably regulated by diapause hormone (DH) and diapause hormone receptor (DHR) that were identified in the silkworm, Bombyx mori and other insects. However, the molecular structure and function of DHR in crustaceans remains unknown. Here, a DHR-like gene from parthenogenetic Artemia (Ar-DHR) was isolated and sequenced. The cDNA sequence consists of 1410bp with a 1260-bp open reading frame encoding a protein consisting of 420 amino acid residues. The results of real-time PCR (qRT-PCR) and Western blot analysis showed that the mRNA and protein of Ar-DHR were mainly expressed at the diapause stage. Furthermore, we found that Ar-DHR was located on the cell membrane of the pre-diapause cyst but in the cytoplasm of the diapause cyst by analysis of immunofluorescence. In vivo knockdown of Ar-DHR by RNA interference (RNAi) and antiserum neutralization consistently inhibited diapause cysts formation. The results indicated that Ar-DHR plays an important role in the induction and maintenance of embryonic diapause in Artemia. Thus, our findings provide an insight into the regulation of diapause formation in Artemia and the function of Ar-DHR.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Amino Acid Sequence genetics
Animals
Bombyx genetics
Bombyx growth & development
Female
Gene Expression Regulation
Insect Proteins genetics
Parthenogenesis genetics
Protein Precursors genetics
RNA Interference
RNA, Messenger genetics
Artemia genetics
Diapause, Insect genetics
Neuropeptides genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5169
- Volume :
- 90
- Database :
- MEDLINE
- Journal :
- Peptides
- Publication Type :
- Academic Journal
- Accession number :
- 28174072
- Full Text :
- https://doi.org/10.1016/j.peptides.2017.01.008