The Homeobox Transcription Factor RHOX10 Drives Mouse Spermatogonial Stem Cell Establishment
Author(s) -
H. C. Song,
Anilkumar Bettegowda,
Blue B. Lake,
A ZHAO,
David Skarbrevik,
Eric Babajanian,
Meena Sukhwani,
Eleen Y. Shum,
Mimi H. Phan,
TerraDawn M. Plank,
Marcy E. Richardson,
Madhuvanthi Ramaiah,
Vaishnavi Sridhar,
Dirk G. de Rooij,
Kyle E. Orwig,
Kun Zhang,
Miles Wilkinson
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.08.090
Subject(s) - homeobox , homeobox a1 , biology , transcription factor , hnf1b , stem cell , homeobox protein nkx 2.5 , phenotype , microbiology and biotechnology , gene , genetics
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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