同源盒
同源框A1
生物
转录因子
干细胞
HNF1B型
同源框蛋白Nkx-2.5
细胞生物学
基因
遗传学
作者
H. C. Song,Anilkumar Bettegowda,Blue B. Lake,Adrienne H. Zhao,David Skarbrevik,Eric Babajanian,Meena Sukhwani,Eleen Y. Shum,Mimi H. Phan,Terra-Dawn M. Plank,Marcy E. Richardson,Madhuvanthi Ramaiah,V. Sridhar,Dirk G. de Rooij,Kyle E. Orwig,Kun Zhang,Miles Wilkinson
出处
期刊:Cell Reports
[Elsevier]
日期:2016-09-01
卷期号:17 (1): 149-164
被引量:49
标识
DOI:10.1016/j.celrep.2016.08.090
摘要
The developmental origins of most adult stem cells are poorly understood. Here, we report the identification of a transcription factor—RHOX10—critical for the initial establishment of spermatogonial stem cells (SSCs). Conditional loss of the entire 33-gene X-linked homeobox gene cluster that includes Rhox10 causes progressive spermatogenic decline, a phenotype indistinguishable from that caused by loss of only Rhox10. We demonstrate that this phenotype results from dramatically reduced SSC generation. By using a battery of approaches, including single-cell-RNA sequencing (scRNA-seq) analysis, we show that Rhox10 drives SSC generation by promoting pro-spermatogonia differentiation. Rhox10 also regulates batteries of migration genes and promotes the migration of pro-spermatogonia into the SSC niche. The identification of an X-linked homeobox gene that drives the initial generation of SSCs has implications for the evolution of X-linked gene clusters and sheds light on regulatory mechanisms influencing adult stem cell generation in general.
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