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m6A控制了压力颗粒中mRNA的长度依赖丰富
Ryan J Ries1, Brian F Pickering1, Hui Xian Poh1
1Department of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY, USA.
Nature structural & molecular biology
|September 14, 2023
概括
N6-甲基氨酸 (m6A) 驱动细胞压力颗粒中长信使RNA (mRNA) 的优先积累. 这一发现揭示了m6A作为mRNA局部化的关键调节器在压力颗粒,独立于单独的长度.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 在RNA生物学,RNA生物学.
背景情况:
- 压力颗粒是细胞压力下形成的动态细胞质焦点.
- 压力颗粒中的信使RNA (mRNA) 通常较长,并富含N6-甲基氨酸 (m6A) 修饰.
- YTHDF蛋白质结合m6A修饰的mRNA,促进它们被招募到压力颗粒中.
研究的目的:
- 研究m6A在压力颗粒中mRNA的长度依赖丰富中的作用.
- 为了确定m6A是否介导长mRNAs的偏好局部化到压力颗粒.
主要方法:
- 在野生类型和m6A缺乏的哺乳动物细胞中的压力颗粒中的mRNA丰富的分析.
- 在mRNA长度,m6A丰富度和压力颗粒局部化之间的相关性分析.
- 研究长外子在m6A形成和随后的mRNA分割中的作用.
主要成果:
- 压力颗粒中的mRNAs的长度依赖丰富是由m6A调节的.
- 在缺乏m6A的细胞中,长mRNA会失去它们在压力颗粒中的优先丰富.
- m6A 丰富度是压力颗粒丰富的更强的预测因素,而不是单独的mRNA长度.
结论:
- mRNA长度与应力颗粒丰富度相关,主要是因为在较长的转录中m6A的流行率更高.
- m6A修饰是mRNA局部化到压力颗粒的关键决定因素,影响细胞应激反应.
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