干细胞.干细胞. m6A mRNA甲基化促进了原始多能性的分化解决
Shay Geula1, Sharon Moshitch-Moshkovitz2, Dan Dominissini3
1The Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
概括
一种酶修改mRNA的Mettl3对于终止老鼠的原始多能性至关重要. 它的缺失导致胚胎致死性,原因是状态终止失败和异常的血统原始化.
科学领域:
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 发展生物学 发展生物学
- 干细胞生物学 干细胞生物学
背景情况:
- 胚胎干细胞中的多能性存在于不同的原始和原始状态.
- 在原始多能和原始多能之间过渡的调节仍然不完全理解.
研究的目的:
- 为了确定分子调节者控制终止的纯粹的多能性.
- 调查N(6) - 甲基氨酸 (m(6) A) 修饰在多能性状态过渡中的作用.
主要方法:
- 产生Mettl3淘汰赛小鼠模型 (植入前表皮质细胞和胚胎干细胞).
- 在mRNA中的m(6) A水平的分析.
- 评估多能状态终结和谱系初始化的评估.
- 在植入后阶段对胚胎死亡率的评估.
主要成果:
- 梅特尔3淘汰赛细胞显示mRNA m(6) A水平降低,但是可行的.
- 这些细胞无法终止纯粹的多能状态.
- 异常和受限制的血统原始发生,导致早期胚胎致死性.
- m(6) 一种修改主要降低了mRNA的稳定性,包括那些促进原始多能性的mRNA.
结论:
- Mettl3对于及时终止小鼠原始多能性至关重要.
- 通过m(6)A的mRNA表观遗传修饰在调节多能性方面发挥着关键的体内作用.
- 已识别的调节模块在功能上对抗原始和初始化的多能性状态.
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