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早期大亚基核糖体中间体的RNA转录后修饰

RNA Post-transcriptional Modifications of an Early-Stage Large-Subunit Ribosomal Intermediate.

作者信息

Narayan Gyan, Gracia Mazuca Luis A, Cho Samuel S, Mohl Jonathon E, Koculi Eda

机构信息

Department of Chemistry and Biochemistry, The University of Texas at El Paso, El Paso, Texas 79968, United States.

Bioinformatics Program, The University of Texas at El Paso, El Paso, Texas 79968, United States.

出版信息

Biochemistry. 2023 Oct 17;62(20):2908-2915. doi: 10.1021/acs.biochem.3c00291. Epub 2023 Sep 26.

Abstract

Protein production by ribosomes is fundamental to life, and proper assembly of the ribosome is required for protein production. The RNA, which is post-transcriptionally modified, provides the platform for ribosome assembly. Thus, a complete understanding of ribosome assembly requires the determination of the RNA post-transcriptional modifications in all of the ribosome assembly intermediates and on each pathway. There are 26 RNA post-transcriptional modifications in 23S RNA of the mature () large ribosomal subunit. The levels of these modifications have been investigated extensively only for a small number of large subunit intermediates and under a limited number of cellular and environmental conditions. In this study, we determined the level of incorporations of 2-methyl adenosine, 3-methyl pseudouridine, 5-hydroxycytosine, and seven pseudouridines in an early-stage large-subunit assembly intermediate with a sedimentation coefficient of 27S. The 27S intermediate is one of three large subunit intermediates accumulated in cells lacking the DEAD-box RNA helicase DbpA and expressing the helicase inactive R331A DbpA construct. The majority of the investigated modifications are incorporated into the 27S large subunit intermediate to similar levels to those in the mature 50S large subunit, indicating that these early modifications or the enzymes that incorporate them play important roles in the initial events of large subunit ribosome assembly.

摘要

核糖体进行蛋白质合成是生命的基础,而核糖体的正确组装是蛋白质合成所必需的。经过转录后修饰的RNA为核糖体组装提供了平台。因此,要全面了解核糖体组装,就需要确定所有核糖体组装中间体以及每条途径中的RNA转录后修饰情况。在成熟的()大核糖体亚基的23S RNA中存在26种RNA转录后修饰。仅在少数大核糖体亚基中间体以及有限的细胞和环境条件下,对这些修饰的水平进行了广泛研究。在本研究中,我们测定了沉降系数为27S的早期大核糖体亚基组装中间体中2-甲基腺苷、3-甲基假尿苷、5-羟胞嘧啶和七种假尿苷的掺入水平。27S中间体是在缺乏DEAD-box RNA解旋酶DbpA并表达解旋酶无活性的R331A DbpA构建体的细胞中积累的三种大核糖体亚基中间体之一。大多数研究的修饰掺入到27S大核糖体亚基中间体中的水平与成熟的50S大核糖体亚基中的水平相似,这表明这些早期修饰或掺入它们的酶在大核糖体亚基组装的初始事件中起重要作用。

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