ArticleCell death and differentiation2026
SMC1A is required for fate determinations of human spermatogonial stem cells and male fertility by interacting with YBX1 and stabilizing HMGA2 mRNA via an m
Article in Cell death and differentiation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
13 authors.
Funding
Abstract
Spermatogonial stem cells (SSCs) are required for initiating and maintaining normal spermatogenesis, and notably, they have significant applications in both reproductive and regenerative medicine owing to their great plasticity with de-differentiation and trans-differentiation potentials. Nevertheless, molecular mechanisms regulating human SSC fate determinations and male fertility remain elusive. Here we report for the first time that structural maintenance of chromosomes 1A (SMC1A) interacts with RNA-binding protein YBX1 to control fate decisions of human SSCs and an association exists between SMC1A dysfunction with male infertility. SMC1A/YBX1 complex stabilizes high mobility group AT-hook 2 (HMGA2) mRNA in an m
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Registered trials
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