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导致不育的单倍不足现象揭示了 TRIM28/KAP1 在精原细胞中的必要性。

Infertility-Causing Haploinsufficiency Reveals TRIM28/KAP1 Requirement in Spermatogonia.

机构信息

Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A(∗)STAR), Singapore 138673, Singapore; NUS Graduate School for Integrative Sciences and Engineering (NGS), National University of Singapore, Singapore 119077, Singapore.

Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A(∗)STAR), Singapore 138673, Singapore.

出版信息

Stem Cell Reports. 2020 May 12;14(5):818-827. doi: 10.1016/j.stemcr.2020.03.013. Epub 2020 Apr 16.

Abstract

Spermatogenesis relies on exquisite stem cell homeostasis, the carefully balanced self-renewal and differentiation of spermatogonial stem cells (SSCs). Disturbing this equilibrium will likely manifest through sub- or infertility, a global health issue with often idiopathic presentation. In this respect, disease phenotypes caused by haploinsufficiency of otherwise vital developmental genes are of particular interest. Here, we show that mice heterozygous for Trim28, an essential epigenetic regulator, suffer gradual testicular degeneration. Contrary to previous reports we detect Trim28 expression in spermatogonia, albeit at low levels. Further reduction through Trim28 heterozygosity increases the propensity of SSCs to differentiate at the cost of self-renewal.

摘要

精子发生依赖于精细的干细胞稳态,精原干细胞(SSC)的自我更新和分化的精细平衡。干扰这种平衡可能表现为亚不育或不育,这是一个具有常见特发性表现的全球健康问题。在这方面,由其他至关重要的发育基因的单倍不足引起的疾病表型特别有趣。在这里,我们表明,Trim28 缺失的杂合子小鼠(一种必需的表观遗传调节剂)会逐渐发生睾丸退化。与之前的报道相反,我们在精原细胞中检测到 Trim28 的表达,尽管水平较低。通过 Trim28 杂合性进一步降低会增加 SSC 分化的倾向,而自我更新的代价增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b46/7220855/ebece249f805/fx1.jpg

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