从60S核糖体子单元中调节释放L13a作为转录特异性翻译控制机制
Barsanjit Mazumder1, Prabha Sampath, Vasudevan Seshadri
1Department of Cell Biology, Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Cell
|October 22, 2003
概括
一种新型的转化沉默机制揭示了,在酸化后,核糖体蛋白L13a会结合于纤维素胺mRNA.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 生物化学 生物化学
背景情况:
- 转录特异性翻译控制依赖于蛋白质结合mRNA的未翻译区域 (UTR).
- 干扰素激活转化抑制剂 (GAIT) 系统在转录后调节基因表达.
研究的目的:
- 阐明一种新型的翻译沉默机制,涉及核糖体蛋白L13a.
- 为了研究L13a在调节青素 (Cp) mRNA翻译中的作用.
主要方法:
- 基因查以确定Cp 3'-UTR结合蛋白.
- 在实验室中使用重组L13a进行翻译试验.
- 在体内研究涉及干扰素-马刺激和分析L13a酸化和核糖体子单元释放.
主要成果:
- 人类核糖体蛋白L13a被确定为Cp mRNA的GAIT.
- 复合L13a在体外抑制了Cp mRNA的翻译.
- 干扰素-诱导L13a酸化和从60S核糖体亚单元释放.
- 释放的L13a特别结合了cp mRNA 3'-UTR GAIT元素,使翻译变得沉默.
结论:
- 核糖体作为调节蛋白质的仓库,调节翻译.
- 核糖体蛋白L13a的调节释放是翻译沉默的关键机制.
- 这一发现扩大了已知的核糖体蛋白的功能,超出了蛋白质合成的范围.
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