Department of Biology, College of Arts and Sciences, Tennessee Technological University, Cookeville, TN, 38505, USA.
Mar Biotechnol (NY). 2024 Nov 23;27(1):6. doi: 10.1007/s10126-024-10387-9.
Sex determination is a fascinating area of research. To date, more than 20 master sex determination (SD) genes have been reported from vertebrate animals. With channel catfish (Ictalurus punctatus), much work has been conducted to determine its master SD gene, ranging from genetic linkage mapping, genome-wide association (GWA) analysis, genome sequencing, comparative genome analysis, epigenomic analysis, transcriptome analysis, and functional studies. Here in this mini review, we provide positional, expression, regulatory, and functional evidence supporting hydin (hydrocephalus-inducing protein or HYDIN axonemal central pair apparatus protein-like) as a master SD gene in channel catfish. Hydin is located within the sex determination region (SDR) within a mapped 8.9-Mb non-recombinational segment on chromosome 4 of channel catfish. It is highly expressed in genetic males, but not in genetic females. The alleles of X and Y are highly differentially methylated with the X chromosome being hypermethylated and the Y chromosome hypomethylated. The hypomethylated Y allele of hydin is expressed while the hypermethylated X allele is not expressed. Such allelic expression fits well with the XY sex determination system of channel catfish. Functional analysis using a methylation blocker, 5-aza-dC, demonstrated that demethylation, especially within the SDR, is accompanied with increased expression of hydin, which led to sex reversal of genetic females into phenotypic males. These evidences support the candidacy of hydin as a master SD gene in channel catfish. Future knockout and analysis of affected genes after hydin knockout should provide insights into how hydin functions as a master SD gene.
性别决定是一个引人入胜的研究领域。迄今为止,已经从脊椎动物中报道了超过 20 个主要性别决定(SD)基因。对于斑点叉尾鮰(Ictalurus punctatus),已经进行了大量工作来确定其主要 SD 基因,包括遗传连锁作图、全基因组关联(GWA)分析、基因组测序、比较基因组分析、表观基因组分析、转录组分析和功能研究。在这篇迷你综述中,我们提供了位置、表达、调控和功能证据,支持 hydin(脑积水诱导蛋白或 HYDIN 轴丝中央对装置蛋白样)作为斑点叉尾鮰的主要 SD 基因。Hydin 位于斑点叉尾鮰第 4 号染色体上 8.9Mb 非重组片段的性别决定区域(SDR)内。它在遗传雄性中高度表达,但在遗传雌性中不表达。X 和 Y 染色体的等位基因高度甲基化差异,X 染色体高度甲基化,Y 染色体低甲基化。hydin 的低甲基化 Y 等位基因表达,而高甲基化的 X 等位基因不表达。这种等位基因表达与斑点叉尾鮰的 XY 性别决定系统非常吻合。使用甲基化抑制剂 5-氮杂胞苷(5-aza-dC)进行功能分析表明,去甲基化,特别是在 SDR 内,伴随着 hydin 表达的增加,导致遗传雌性转变为表型雄性。这些证据支持 hydin 作为斑点叉尾鮰主要 SD 基因的候选性。在 hydin 敲除后进行 knock-out 和受影响基因的分析,应该可以深入了解 hydin 如何作为主要 SD 基因发挥作用。