| Literature DB >> 27681428 |
Hye-Won Song1, Anilkumar Bettegowda1, Blue B Lake2, Adrienne H Zhao1, David Skarbrevik1, Eric Babajanian1, Meena Sukhwani3, Eleen Y Shum1, Mimi H Phan1, Terra-Dawn M Plank1, Marcy E Richardson1, Madhuvanthi Ramaiah1, Vaishnavi Sridhar1, Dirk G de Rooij4, Kyle E Orwig3, Kun Zhang2, Miles F Wilkinson5.
Abstract
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.Entities:
Keywords: Rhox; germ cell; germ line stem cell; gonocytes; homeobox; prospermatogonia; spermatogenesis; spermatogonia; spermatogonial stem cells; transcription factor
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Year: 2016 PMID: 27681428 PMCID: PMC5063083 DOI: 10.1016/j.celrep.2016.08.090
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423