State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Science, Hunan Normal University, Changsha, China; INRAE, LPGP, 35000 Rennes, France.
INRAE, LPGP, 35000 Rennes, France; Department of Ecology and Evolution, University of Lausanne, Switzerland.
Gene. 2023 Jan 20;850:146933. doi: 10.1016/j.gene.2022.146933. Epub 2022 Sep 30.
Channel catfish is an important species for aquaculture that exhibits a sexually dimorphic growth in favor of males. Genetic sexing and development of sex markers are crucial for the early identification of sex and of particular genotypes (YY males) for the production of all-male population in channel catfish aquaculture. In this study, we sequenced genomic DNA from pools of males and pools of females to better characterize the sex determining region (SDR) of channel catfish and to develop sex-specific markers for genetic sexing. Performing comparative analyses on male and female pooled genomic reads, we identified a large SDR (∼8.3 Mb) in the middle of channel catfish linkage group 4 (LG04). This non-recombining SDR contains a high-density of male-specific (Y chromosome) fixed single nucleotide polymorphisms (SNPs) along with ∼ 185 kb male-specific insertions or deletions. This SDR contains 95 annotated protein-encoding genes, including the recently reported putative channel catfish master sex determining (MSD) gene, breast cancer anti-estrogen resistance protein 1 (bcar1), located at one edge of the SDR. No sex-specific SNPs and/or indels were found in the coding sequence of bcar1, but one male-specific SNP was identified in its first intron. Based on this genomic information, we developed a PCR-based sex-specific genetic test. Genotyping results confirmed strong linkage between phenotypic sexes and the identified SDR in channel catfish. Our results confirm, using a Pool-Seq approach, that channel catfish is male heterogametic (XX-XY) with a large SDR on the LG04 sex chromosome. Furthermore, our genotyping primers can be used to identify XX, XY, and YY fish that will facilitate future research on sex determination and aquaculture applications in channel catfish.
斑点叉尾鮰是一种重要的水产养殖物种,表现出有利于雄性的性二型生长。遗传性别鉴定和性标记的发展对于早期识别性别和特定基因型(YY 雄性)至关重要,这些特定基因型可用于生产斑点叉尾鮰水产养殖中的全雄种群。在本研究中,我们对雄性和雌性群体的基因组 DNA 进行了测序,以更好地描述斑点叉尾鮰的性别决定区域 (SDR),并开发用于遗传性别鉴定的性别特异性标记。通过对雄性和雌性群体基因组读段进行比较分析,我们在斑点叉尾鮰连锁群 4 (LG04) 的中间位置鉴定出一个大的 SDR(约 8.3 Mb)。这个非重组的 SDR 包含高密度的雄性特异性(Y 染色体)固定单核苷酸多态性 (SNP),以及约 185 kb 的雄性特异性插入或缺失。这个 SDR 包含 95 个注释的蛋白质编码基因,包括最近报道的假定斑点叉尾鮰主性别决定(MSD)基因乳腺癌抗雌激素耐药蛋白 1 (bcar1),位于 SDR 的一个边缘。在 bcar1 的编码序列中没有发现性别特异性 SNP 和/或插入缺失,但在其第一个内含子中发现了一个雄性特异性 SNP。基于这些基因组信息,我们开发了一种基于 PCR 的性别特异性遗传测试。基因分型结果证实了斑点叉尾鮰表型性别与鉴定的 SDR 之间存在强烈的连锁关系。我们的研究结果通过 Pool-Seq 方法证实,斑点叉尾鮰是雄性异型(XX-XY),LG04 性染色体上有一个大的 SDR。此外,我们的基因分型引物可用于鉴定 XX、XY 和 YY 鱼,这将有助于未来对斑点叉尾鮰性别决定和水产养殖应用的研究。