Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences (CAFS), Qingdao 266071, China; Laboratory for Marine Fisheries Science and Food Production Processes, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao 266237, China.
Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences (CAFS), Qingdao 266071, China; Laboratory for Marine Fisheries Science and Food Production Processes, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao 266237, China.
Comp Biochem Physiol Part D Genomics Proteomics. 2021 Dec;40:100919. doi: 10.1016/j.cbd.2021.100919. Epub 2021 Sep 30.
Sex differentiation in aquatic fish is important both for theoretical study and practical production, as growth dimorphism frequently appears in different sexes, especially in marine fish. The deciphered genome, identification of the male-determining gene dmrt1 and established genotypic sex screening method make Chinese tongue sole (Cynoglossus semilaevis) an ideal model to study sex differentiation in fish. In this study, comparative gonadal transcriptomic analyses were conducted for genetic females and males at 48, 68, and 108 days post hatching (dph), representing pre-, during- and post-gonadal differentiation stages, although the gonad is not completely differentiated and isolable in 48 and 68 dph individuals, while it is in 108 dph individuals. Altogether, 28 libraries were constructed, and a mean of 46.64 M clean reads was obtained. Differentially expressed gene (DEG) analysis revealed that 179 genes had similar expression patterns in males and females in all three stages. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis suggested that the enriched pathways included ubiquitin-mediated proteolysis, lysosomes, and RNA degradation. Moreover, weighted gene coexpression network analyses (WGCNA) identified 14 modules, one of which was closely correlated with female differentiation, exhibiting female-biased expression in all three stages (48, 68, 108 dph). An illustrated core gene interaction network of this module identified 50 genes, most of which are on W chromosomes. Six genes, including two ubiquitin conjugating enzymes, were selected for further investigation, and their female-biased expression was confirmed in even earlier stages, at 10 and 30 dph. These data facilitate our understanding of sex differentiation in fish and provide a genomic rationale for screening candidate genes (preferentially W-linked genes) that could be involved in the female differentiation process.
鱼类的性别分化在理论研究和实际生产中都很重要,因为不同性别的生长二态性经常出现,尤其是在海洋鱼类中。已破译的基因组、雄性决定基因 dmrt1 的鉴定以及建立的基因型性别筛选方法,使中国舌鳎(Cynoglossus semilaevis)成为研究鱼类性别分化的理想模型。在这项研究中,对孵化后 48、68 和 108 天(dph)的遗传雌性和雄性的性腺转录组进行了比较分析,分别代表性腺分化前、中、后期,尽管在 48 和 68 dph 个体中,性腺尚未完全分化和可分离,而在 108 dph 个体中则是可分离的。总共构建了 28 个文库,平均获得了 46.64 M 清洁读取量。差异表达基因(DEG)分析显示,在所有三个阶段,179 个基因在雄性和雌性中具有相似的表达模式。京都基因与基因组百科全书(KEGG)分析表明,富集的途径包括泛素介导的蛋白水解、溶酶体和 RNA 降解。此外,加权基因共表达网络分析(WGCNA)鉴定了 14 个模块,其中一个与雌性分化密切相关,在所有三个阶段(48、68、108 dph)均表现出雌性偏倚表达。该模块的一个有插图的核心基因相互作用网络确定了 50 个基因,其中大多数位于 W 染色体上。选择了包括两个泛素连接酶在内的 6 个基因进行进一步研究,证实它们在更早的阶段(10 和 30 dph)也表现出雌性偏倚表达。这些数据有助于我们了解鱼类的性别分化,并为筛选可能参与雌性分化过程的候选基因(优先为 W 连锁基因)提供基因组依据。