KDM3A和KDM3B通过对替代分离的调节来维持纯粹的多能性
Caleb M Dillingham1,2,3, Harshini Cormaty1,2,4, Ellen C Morgan1,2
1Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI, 53715, USA.
bioRxiv : the preprint server for biology
|July 3, 2023
概括
基因组脱甲基酶KDM3A和KDM3B通过改变RNA剪接来调节细胞身份,而不仅仅是基因抑制. 这种意想不到的作用通过修改关键发育因素的拼接模式来维持多能性.
科学领域:
- 表观遗传学和基因调控
- 干细胞生物学 干细胞生物学
- 在RNA生物学,RNA生物学.
背景情况:
- 基斯修饰酶对于细胞的识别和转录至关重要.
- 胚胎干细胞 (ESC) 认同依赖于低基因抑制的差异化响应.
- 甲基酶KDM3家族去除压制性的H3K9me2标记.
结论:
- KDM3蛋白具有超出基因组脱甲基化之外的非正规作用.
- 通过剪接进行后转录调节是KDM3维持多能性的新机制.
- 这些发现重新定义了基因组甲基酶在细胞身份调节中的功能.
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