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本文引用的文献

1
Cryo-electron microscopy structure of the 30S subunit in complex with the YjeQ biogenesis factor.冷冻电镜结构的 30S 亚基与 YjeQ 生物发生因子复合物。
RNA. 2011 Nov;17(11):2026-38. doi: 10.1261/rna.2922311. Epub 2011 Sep 29.
2
Structural basis for the function of a small GTPase RsgA on the 30S ribosomal subunit maturation revealed by cryoelectron microscopy.冷冻电镜解析小 GTP 酶 RsgA 调控 30S 核糖体亚基成熟的结构基础
Proc Natl Acad Sci U S A. 2011 Aug 9;108(32):13100-5. doi: 10.1073/pnas.1104645108. Epub 2011 Jul 25.
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Assembly of bacterial ribosomes.细菌核糖体的组装。
Annu Rev Biochem. 2011;80:501-26. doi: 10.1146/annurev-biochem-062608-160432.
4
Understanding ribosome assembly: the structure of in vivo assembled immature 30S subunits revealed by cryo-electron microscopy.理解核糖体组装:通过冷冻电镜观察到体内组装的不成熟 30S 亚基的结构。
RNA. 2011 Apr;17(4):697-709. doi: 10.1261/rna.2509811. Epub 2011 Feb 8.
5
RsgA releases RbfA from 30S ribosome during a late stage of ribosome biosynthesis.RsgA 在核糖体生物合成的晚期将 RbfA 从 30S 核糖体上释放出来。
EMBO J. 2011 Jan 5;30(1):104-14. doi: 10.1038/emboj.2010.291. Epub 2010 Nov 23.
6
Quantitative proteomic analysis of ribosome assembly and turnover in vivo.体内核糖体组装和周转的定量蛋白质组学分析。
J Mol Biol. 2010 Oct 29;403(3):331-45. doi: 10.1016/j.jmb.2010.08.005. Epub 2010 Aug 13.
7
Role of GTPases in bacterial ribosome assembly.GTP酶在细菌核糖体组装中的作用。
Annu Rev Microbiol. 2009;63:155-76. doi: 10.1146/annurev.micro.091208.073225.
8
Deconstructing ribosome construction.解析核糖体的构建
Trends Biochem Sci. 2009 May;34(5):256-63. doi: 10.1016/j.tibs.2009.01.011. Epub 2009 Apr 17.
9
The RimP protein is important for maturation of the 30S ribosomal subunit.RimP蛋白对30S核糖体亚基的成熟很重要。
J Mol Biol. 2009 Feb 27;386(3):742-53. doi: 10.1016/j.jmb.2008.12.076. Epub 2009 Jan 6.
10
Quantitative ESI-TOF analysis of macromolecular assembly kinetics.大分子组装动力学的定量电喷雾电离飞行时间质谱分析
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大肠杆菌 rimM 和 yjeQ 缺失株积累相似结构和蛋白质组成的不成熟 30S 亚基。

Escherichia coli rimM and yjeQ null strains accumulate immature 30S subunits of similar structure and protein complement.

机构信息

Department of Biochemistry and Biomedical Sciences, and M.G. DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, Ontario, L8N3Z5, Canada.

出版信息

RNA. 2013 Jun;19(6):789-802. doi: 10.1261/rna.037523.112. Epub 2013 Apr 23.

DOI:10.1261/rna.037523.112
PMID:23611982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3683913/
Abstract

Assembly of the Escherichia coli 30S ribosomal subunits proceeds through multiple parallel pathways. The protein factors RimM, YjeQ, RbfA, and Era work in conjunction to assist at the late stages of the maturation process of the small subunit. However, it is unclear how the functional interplay between these factors occurs in the context of multiple parallel pathways. To understand how these factors work together, we have characterized the immature 30S subunits that accumulate in ΔrimM cells and compared them with immature 30S subunits from a ΔyjeQ strain. The cryo-EM maps obtained from these particles showed that the densities representing helices 44 and 45 in the rRNA were partially missing, suggesting mobility of these motifs. These 30S subunits were also partially depleted in all tertiary ribosomal proteins, particularly those binding in the head domain. Using image classification, we identified four subpopulations of ΔrimM immature 30S subunits differing in the amount of missing density for helices 44 and 45, as well as the amount of density existing in these maps for the underrepresented proteins. The structural defects found in these immature subunits resembled those of the 30S subunits that accumulate in the ΔyjeQ strain. These findings are consistent with an "early convergency model" in which multiple parallel assembly pathways of the 30S subunit converge into a late assembly intermediate, as opposed to the mature state. Functionally related factors will bind to this intermediate to catalyze the last steps of maturation leading to the mature 30S subunit.

摘要

大肠杆菌 30S 核糖体亚基的组装是通过多个平行途径进行的。蛋白质因子 RimM、YjeQ、RbfA 和 Era 协同作用,协助小亚基成熟过程的后期阶段。然而,这些因素在多个平行途径的背景下如何相互作用尚不清楚。为了了解这些因素如何协同工作,我们对在 ΔrimM 细胞中积累的不成熟 30S 亚基进行了表征,并将其与来自 ΔyjeQ 菌株的不成熟 30S 亚基进行了比较。从这些颗粒获得的 cryo-EM 图谱显示,rRNA 中代表螺旋 44 和 45 的密度部分缺失,表明这些基序的移动性。这些 30S 亚基也部分缺乏所有三级核糖体蛋白,特别是那些结合在头部结构域的蛋白。通过图像分类,我们鉴定了 4 种不同 ΔrimM 不成熟 30S 亚基的亚群,这些亚基的区别在于螺旋 44 和 45 的缺失密度以及这些图谱中代表性不足的蛋白质的密度存在量。这些不成熟亚基中的结构缺陷与在 ΔyjeQ 菌株中积累的 30S 亚基相似。这些发现与“早期收敛模型”一致,即 30S 亚基的多个平行组装途径收敛到一个晚期组装中间体,而不是成熟状态。功能相关的因子将结合到这个中间体上,催化成熟过程的最后几步,从而产生成熟的 30S 亚基。