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Cloning and characterization of rec8 gene in orange-spotted grouper (Epinephelus coioides) and Dmrt1 regulation of rec8 promoter activity.
Wang, Qing; Lin, Fangmei; He, Qi; Huang, Qifeng; Duan, Xuzhuo; Liu, Xiaochun; Xiao, Shiqiang; Yang, Huirong; Zhao, HuiHong.
Afiliación
  • Wang Q; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
  • Lin F; Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou, 510642, People's Republic of China.
  • He Q; Joint Laboratory of Guangdong Province and Hong Kong Region on Marine Bioresource Conservation and Exploitation, Guangzhou, 510642, People's Republic of China.
  • Huang Q; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
  • Duan X; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
  • Liu X; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
  • Xiao S; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
  • Yang H; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
  • Zhao H; College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
Fish Physiol Biochem ; 47(2): 393-407, 2021 Apr.
Article en En | MEDLINE | ID: mdl-33547601
Meiosis is a specialized type of cell division critical for gamete production during sexual reproduction in eukaryotes. The meiotic recombination protein Rec8 has been identified as an important factor in germ cell meiotic initiation in vertebrates; however, its equivalent role in teleosts is poorly characterized. In this study, we cloned and sequenced the rec8 gene from orange-spotted grouper (Epinephelus coioides). The cDNA sequence consisted of 2244 base pairs (bp), including a 5' untranslated region (UTR) of 198 bp and a 3'UTR of 284 bp. The open reading frame of grouper rec8 was 1752 bp, encoding 584 amino acids. Expression levels of rec8 were higher in the ovary, intersex gonad, and testis. A neighbor-joining phylogenetic tree based on the deduced amino acid sequence indicated a common origin for grouper and other teleost rec8 molecules. Immunohistochemistry using a polyclonal anti-Rec8 antibody localized the protein in the oogonia and primary oocytes in the ovary and in spermatogonia and spermatocytes in the intersex gonad and testis, suggesting that Rec8 may play an important role in the meiotic division and the development of grouper germ cells. In addition, we found that the transcription factor Dmrt1 increased rec8 promoter activity through the second binding site, based on dual-luciferase assays. Together, these results suggest that Rec8 plays a crucial role in meiosis and may be regulated by Dmrt1 to affect meiosis in groupers.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Perciformes / Clonación Molecular / Proteínas de Ciclo Celular Tipo de estudio: Prognostic_studies Idioma: En Revista: Fish Physiol Biochem Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Perciformes / Clonación Molecular / Proteínas de Ciclo Celular Tipo de estudio: Prognostic_studies Idioma: En Revista: Fish Physiol Biochem Año: 2021 Tipo del documento: Article