Germline sex determination regulates sex-specific signaling between germline stem cells and their niche

被引:12
作者
Bhaskar, Pradeep Kumar [1 ]
Southard, Sheryl [1 ,2 ]
Baxter, Kelly [1 ]
Van Doren, Mark [1 ]
机构
[1] Johns Hopkins Univ, Dept Biol, 3400 N Charles St, Baltimore, MD 21218 USA
[2] Seraxis Inc, 20271 Goldenrod Lane,Ste 2085, Germantown, MD 20876 USA
关键词
SELF-RENEWAL; DROSOPHILA-MELANOGASTER; DOSAGE COMPENSATION; LETHAL; STAT; GENE; LINE; MAINTENANCE; ACTIVATION; SOMA;
D O I
10.1016/j.celrep.2022.110620
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Establishing germ cell sexual identity is critical for development of male and female germline stem cells (GSCs) and production of sperm or eggs. Germ cells depend on signals from the somatic gonad to determine sex, but in organisms such as flies, mice, and humans, the sex chromosome genotype of the germ cells is also important for germline sexual development. How somatic signals and germ-cell-intrinsic cues combine to regulate germline sex determination is thus a key question. We find that JAK/STAT signaling in the GSC niche promotes male identity in germ cells, in part by activating the chromatin reader Phf7. Further, we find that JAK/STAT signaling is blocked in XX (female) germ cells through the action of the sex determination gene Sex lethal to preserve female identity. Thus, an important function of germline sexual identity is to control how GSCs respond to signals in their niche environment.
引用
收藏
页数:21
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