Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA.
Department of Biological Sciences, Northern Arizona University, Flagstaff, AZ 86011, USA.
Genetics. 2021 Feb 9;217(2). doi: 10.1093/genetics/iyaa030.
People with NR5A1 mutations experience testicular dysgenesis, ovotestes, or adrenal insufficiency, but we do not completely understand the origin of this phenotypic diversity. NR5A1 is expressed in gonadal soma precursor cells before expression of the sex-determining gene SRY. Many fish have two co-orthologs of NR5A1 that likely partitioned ancestral gene subfunctions between them. To explore ancestral roles of NR5A1, we knocked out nr5a1a and nr5a1b in zebrafish. Single-cell RNA-seq identified nr5a1a-expressing cells that co-expressed genes for steroid biosynthesis and the chemokine receptor Cxcl12a in 1-day postfertilization (dpf) embryos, as does the mammalian adrenal-gonadal (interrenal-gonadal) primordium. In 2dpf embryos, nr5a1a was expressed stronger in the interrenal-gonadal primordium than in the early hypothalamus but nr5a1b showed the reverse. Adult Leydig cells expressed both ohnologs and granulosa cells expressed nr5a1a stronger than nr5a1b. Mutants for nr5a1a lacked the interrenal, formed incompletely differentiated testes, had no Leydig cells, and grew far larger than normal fish. Mutants for nr5a1b formed a disorganized interrenal and their gonads completely disappeared. All homozygous mutant genotypes lacked secondary sex characteristics, including male breeding tubercles and female sex papillae, and had exceedingly low levels of estradiol, 11-ketotestosterone, and cortisol. RNA-seq showed that at 21dpf, some animals were developing as females and others were not, independent of nr5a1 genotype. By 35dpf, all mutant genotypes greatly under-expressed ovary-biased genes. Because adult nr5a1a mutants form gonads but lack an interrenal and conversely, adult nr5a1b mutants lack a gonad but have an interrenal, the adrenal, and gonadal functions of the ancestral nr5a1 gene partitioned between ohnologs after the teleost genome duplication, likely owing to reciprocal loss of ancestral tissue-specific regulatory elements. Identifying such elements could provide hints to otherwise unexplained cases of Differences in Sex Development.
患有 NR5A1 突变的人会出现睾丸发育不良、卵巢睾、或肾上腺功能不全,但我们不完全了解这种表型多样性的起源。NR5A1 在表达性别决定基因 SRY 之前,在性腺体祖细胞中表达。许多鱼类有两个 NR5A1 的共同直系同源物,它们可能在它们之间分配了祖先基因的亚功能。为了探索 NR5A1 的祖先作用,我们在斑马鱼中敲除了 nr5a1a 和 nr5a1b。单细胞 RNA-seq 鉴定出在 1 天孵化后(dpf)胚胎中与类固醇生物合成和趋化因子受体 Cxcl12a 共表达的 nr5a1a 表达细胞,如哺乳动物的肾上腺-性腺(肾上腺-性腺)原基。在 2dpf 胚胎中,nr5a1a 在肾上腺-性腺原基中的表达强于早期下丘脑,但 nr5a1b 则相反。成年 Leydig 细胞表达两个同源物,颗粒细胞表达 nr5a1a 强于 nr5a1b。nr5a1a 突变体缺乏肾上腺,形成不完全分化的睾丸,没有 Leydig 细胞,并且比正常鱼类生长得大得多。nr5a1b 突变体形成一个组织紊乱的肾上腺,它们的性腺完全消失。所有纯合突变基因型均缺乏第二性征,包括雄性繁殖结节和雌性性乳头,并且雌二醇、11-酮睾酮和皮质醇水平极低。RNA-seq 显示,在 21dpf 时,一些动物发育为雌性,而另一些动物则没有,与 nr5a1 基因型无关。到 35dpf 时,所有突变基因型的卵巢偏向基因表达大大降低。由于成年 nr5a1a 突变体形成性腺但缺乏肾上腺,而相反,成年 nr5a1b 突变体缺乏性腺但具有肾上腺、性腺,因此在硬骨鱼基因组加倍后,祖先 nr5a1 基因的肾上腺和性腺功能在同源物之间分配,可能是由于祖先组织特异性调节元件的相互缺失。鉴定这些元件可以为其他未解释的性别发育差异提供线索。