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细胞周期蛋白依赖性激酶抑制剂 1A mRNA 的上游开放阅读框负调控下游主要开放阅读框的翻译。

The upstream open reading frame of cyclin-dependent kinase inhibitor 1A mRNA negatively regulates translation of the downstream main open reading frame.

机构信息

School of Life Sciences and Biotechnology, Korea University, Seoul 136-701, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2012 Aug 3;424(3):469-75. doi: 10.1016/j.bbrc.2012.06.135. Epub 2012 Jul 4.

Abstract

The first round of translation occurs on mRNAs bound by nuclear cap-binding complex (CBC), which is composed of nuclear cap-binding protein 80 and 20 (CBP80/20). During this round of translation, aberrant mRNAs are recognized and downregulated in abundance by nonsense-mediated mRNA decay (NMD), which is one of the mRNA quality control mechanisms. Here, our microarray analysis reveals that the level of cyclin-dependent kinase inhibitor 1A (CDKN1A; also known as Waf1/p21) mRNAs increases in cells depleted of cellular NMD factors. Intriguingly, CDKN1A mRNA contains an upstream open reading frame (uORF), which is a NMD-inducing feature. Using chimeric reporter constructs, we find that the uORF of CDKN1A mRNA negatively modulates translation of the main downstream ORF. These findings provide biological insights into the possible role of NMD in diverse biological pathways mediated by CDKN1A.

摘要

第一轮翻译发生在与核帽结合复合物(CBC)结合的 mRNAs 上,该复合物由核帽结合蛋白 80 和 20(CBP80/20)组成。在这轮翻译中,通过无意义介导的 mRNA 降解(NMD),异常的 mRNAs 被识别并大量下调,这是 mRNA 质量控制机制之一。在这里,我们的微阵列分析表明,在耗尽细胞 NMD 因子的细胞中,细胞周期蛋白依赖性激酶抑制剂 1A(CDKN1A;也称为 Waf1/p21)mRNA 的水平增加。有趣的是,CDKN1A mRNA 包含一个上游开放阅读框(uORF),这是一个 NMD 诱导特征。使用嵌合报告基因构建体,我们发现 CDKN1A mRNA 的 uORF 负调节下游主要 ORF 的翻译。这些发现为 NMD 在由 CDKN1A 介导的多种生物学途径中的可能作用提供了生物学见解。

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