The silver-lipped pearl oyster(Pinctada maxima)is the largest and most commercially valuable pearl-producing oyster,renowned for its ability to generate large,lustrous pearls.This species is a sequential hermaphrodite...The silver-lipped pearl oyster(Pinctada maxima)is the largest and most commercially valuable pearl-producing oyster,renowned for its ability to generate large,lustrous pearls.This species is a sequential hermaphrodite,with pearl production displaying notable sexual dimorphism.Consequently,understanding the molecular mechanisms governing sex determination and differentiation is crucial for advancing breeding strategies in the pearl oyster industry.To elucidate these mechanisms,this study conducted integrative transcriptomic analyses of P.maxima gonadal tissues using isoform sequencing(Isoseq)and RNA sequencing(RNA-seq).Comparative analysis of ovarian and testicular tissues identified 2768 differentially expressed genes(DEGs).Gene coexpression network analysis delineated four key modules,including three sex-specific modules and one shared module.Key genes implicated in sex determination and maintenance were identified,including FOXL2,NANOS1,andβ-catenin,important for ovarian maintenance,and DMRT,SOX30,FEM1,and FOXJ1,crucial for testicular maintenance.These genes,widely studied in other taxa,were confirmed as hub genes in the sex-related modules of P.maxima.Interestingly,genes within the shared module were significantly enriched in the spliceosome pathway.Alternative splicing analysis highlighted its extensive role in gonadal tissues,with more pronounced activity observed in the testis compared to the ovary.Nearly half(47.83%,375)of the identified genes undergoing differential alternative splicing(DASGs)also exhibited differential transcript usage(DTUGs),while only 17%of DTUGs overlapped with DEGs.Genes associated with sex differentiation,such as DMRT,β-catenin,and U2AF2,displayed sex-specific and/or sex-biased isoforms.These findings offer novel insights into the molecular basis of sex differentiation in P.maxima,which could inform the development of targeted breeding strategies aimed at sex control,thereby enhancing pearl quality and yield in aquaculture.This study offers a robust molecular foundation for advancing breeding programs and optimizing production in the pearl oyster industry.展开更多
采用聚丙烯酰胺凝胶垂直板电泳(PAGE)技术,对11株Ei meria maxima和1株E.tenella的孢子化卵囊,进行了乳酸脱氢酶(LDH)、葡萄糖磷酸异构酶(GPI)、葡萄糖-6-磷酸脱氢酶(G6PD)、葡萄糖磷酸变位酶(PGM)和苹果酸脱氢酶(MDH)的同工酶分析。试...采用聚丙烯酰胺凝胶垂直板电泳(PAGE)技术,对11株Ei meria maxima和1株E.tenella的孢子化卵囊,进行了乳酸脱氢酶(LDH)、葡萄糖磷酸异构酶(GPI)、葡萄糖-6-磷酸脱氢酶(G6PD)、葡萄糖磷酸变位酶(PGM)和苹果酸脱氢酶(MDH)的同工酶分析。试验结果显示,E.maxima和E.tenella在LDH、GPI、G6PD、PGM和MDH的酶谱上有明显差异,而在11株E.maxima之间无差异,表明E.maxima的酶变异相当保守。展开更多
基金supported by the Hainan Province Science and Technology Talent Innovation Project(KJRC2023A02)Project of Sanya Yazhouwan Science and Technology City Management Foundation(SKJC-KJ-2019KY01)Sanya Science and Technology Special Fund(2022KJCX91)。
文摘The silver-lipped pearl oyster(Pinctada maxima)is the largest and most commercially valuable pearl-producing oyster,renowned for its ability to generate large,lustrous pearls.This species is a sequential hermaphrodite,with pearl production displaying notable sexual dimorphism.Consequently,understanding the molecular mechanisms governing sex determination and differentiation is crucial for advancing breeding strategies in the pearl oyster industry.To elucidate these mechanisms,this study conducted integrative transcriptomic analyses of P.maxima gonadal tissues using isoform sequencing(Isoseq)and RNA sequencing(RNA-seq).Comparative analysis of ovarian and testicular tissues identified 2768 differentially expressed genes(DEGs).Gene coexpression network analysis delineated four key modules,including three sex-specific modules and one shared module.Key genes implicated in sex determination and maintenance were identified,including FOXL2,NANOS1,andβ-catenin,important for ovarian maintenance,and DMRT,SOX30,FEM1,and FOXJ1,crucial for testicular maintenance.These genes,widely studied in other taxa,were confirmed as hub genes in the sex-related modules of P.maxima.Interestingly,genes within the shared module were significantly enriched in the spliceosome pathway.Alternative splicing analysis highlighted its extensive role in gonadal tissues,with more pronounced activity observed in the testis compared to the ovary.Nearly half(47.83%,375)of the identified genes undergoing differential alternative splicing(DASGs)also exhibited differential transcript usage(DTUGs),while only 17%of DTUGs overlapped with DEGs.Genes associated with sex differentiation,such as DMRT,β-catenin,and U2AF2,displayed sex-specific and/or sex-biased isoforms.These findings offer novel insights into the molecular basis of sex differentiation in P.maxima,which could inform the development of targeted breeding strategies aimed at sex control,thereby enhancing pearl quality and yield in aquaculture.This study offers a robust molecular foundation for advancing breeding programs and optimizing production in the pearl oyster industry.
文摘采用聚丙烯酰胺凝胶垂直板电泳(PAGE)技术,对11株Ei meria maxima和1株E.tenella的孢子化卵囊,进行了乳酸脱氢酶(LDH)、葡萄糖磷酸异构酶(GPI)、葡萄糖-6-磷酸脱氢酶(G6PD)、葡萄糖磷酸变位酶(PGM)和苹果酸脱氢酶(MDH)的同工酶分析。试验结果显示,E.maxima和E.tenella在LDH、GPI、G6PD、PGM和MDH的酶谱上有明显差异,而在11株E.maxima之间无差异,表明E.maxima的酶变异相当保守。
