在uORF2/ATF4重叠中的茎环诱导的核糖体排队微调压力诱导的人类ATF4转化控制
Anna M Smirnova1, Vladislava Hronová1, Mahabub Pasha Mohammad1
1Laboratory of Regulation of Gene Expression, Institute of Microbiology of the Czech Academy of Sciences, Videnska 1083, 142 20 Prague, Czech Republic.
Cell reports
|March 20, 2024
概括
激活转录因子4 (ATF4) 翻译比以前认为的要复杂得多. 新发现显示,核糖体排队和漏洞扫描机制在细胞应激下调节ATF4,影响细胞命运.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 基因规则 基因规则
背景情况:
- 激活转录因子4 (ATF4) 是综合应激反应的关键调节者.
- ATF4的诱导主要归因于通过上游开放阅读框架1 (uORF1) 的翻译重新启动.
研究的目的:
- 调查控制ATF4翻译超出已建立的uORF1模型的替代监管机制.
- 在细胞应激条件下阐明ATF4复杂的翻译控制.
主要方法:
- 在ATF4mRNA中保存序列元素的生物信息分析.
- 使用核糖体排队和漏洞扫描模型研究核糖体动力学.
- 在监管区域内识别保存的改性腺因.
主要成果:
- 在uORF2/ATF4重叠中,一个保存的干环和近同类的CUG通过核糖体队列来调节翻译.
- 这种机制解释了抑制性uORF2的压力诱导翻译,挑战了对uORF1.1的唯一依赖.
- 确定了两种具有对立作用的保存腺素,并且在正规起始点有显著的泄漏扫描.
结论:
- ATF4的翻译控制比以前理解的要复杂得多,涉及多个监管层.
- 这些复杂的机制微调ATF4表达,这对细胞适应或死亡途径至关重要.
- 了解这些调节路径对于理解ATF4在各种生物过程中的作用至关重要.
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