Department of Biology, Johns Hopkins University, Baltimore, Maryland, United States of America.
PLoS Genet. 2019 Jul 22;15(7):e1007617. doi: 10.1371/journal.pgen.1007617. eCollection 2019 Jul.
For sexually reproducing organisms, production of male or female gametes depends on specifying the correct sexual identity in the germline. In D. melanogaster, Sex lethal (Sxl) is the key gene that controls sex determination in both the soma and the germline, but how it does so in the germline is unknown, other than that it is different than in the soma. We conducted an RNA expression profiling experiment to identify direct and indirect germline targets of Sxl specifically in the undifferentiated germline. We find that, in these cells, Sxl loss does not lead to a global masculinization observed at the whole-genome level. In contrast, Sxl appears to affect a discrete set of genes required in the male germline, such as Phf7. We also identify Tudor domain containing protein 5-like (Tdrd5l) as a target for Sxl regulation that is important for male germline identity. Tdrd5l is repressed by Sxl in female germ cells, but is highly expressed in male germ cells where it promotes proper male fertility and germline differentiation. Additionally, Tdrd5l localizes to cytoplasmic granules with some characteristics of RNA Processing (P-) Bodies, suggesting that it promotes male identity in the germline by regulating post-transcriptional gene expression.
对于有性繁殖的生物来说,雄性或雌性配子的产生取决于生殖细胞中正确的性别身份指定。在黑腹果蝇中,性致死(Sxl)是控制躯体和生殖细胞性别决定的关键基因,但它在生殖细胞中是如何做到这一点的,除了与躯体不同之外,我们一无所知。我们进行了一项 RNA 表达谱实验,以鉴定 Sxl 在未分化生殖细胞中直接和间接的生殖细胞靶标。我们发现,在这些细胞中,Sxl 的缺失不会导致在全基因组水平上观察到的全局性雄性化。相比之下,Sxl 似乎影响了一组离散的雄性生殖细胞所必需的基因,如 Phf7。我们还鉴定出 Tudor 结构域蛋白 5 样(Tdrd5l)作为 Sxl 调控的靶标,这对于雄性生殖细胞身份至关重要。Tdrd5l 在雌性生殖细胞中被 Sxl 抑制,但在雄性生殖细胞中高度表达,它促进了正常的雄性生育力和生殖细胞分化。此外,Tdrd5l 定位于具有某些 RNA 处理(P)体特征的细胞质颗粒中,表明它通过调节转录后基因表达来促进生殖细胞中的雄性身份。