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本文引用的文献

1
Dom34:Hbs1 promotes subunit dissociation and peptidyl-tRNA drop-off to initiate no-go decay.Dom34:Hbs1 促进亚基解离和肽酰-tRNA 脱落,以启动无意义衰变。
Science. 2010 Oct 15;330(6002):369-72. doi: 10.1126/science.1192430.
2
The role of ABCE1 in eukaryotic posttermination ribosomal recycling.ABCE1 在真核生物终止后核糖体循环中的作用。
Mol Cell. 2010 Jan 29;37(2):196-210. doi: 10.1016/j.molcel.2009.12.034.
3
The mechanism of eukaryotic translation initiation and principles of its regulation.真核生物翻译起始的机制与调控原则。
Nat Rev Mol Cell Biol. 2010 Feb;11(2):113-27. doi: 10.1038/nrm2838.
4
The genetic landscape of a cell.细胞的基因图谱。
Science. 2010 Jan 22;327(5964):425-31. doi: 10.1126/science.1180823.
5
Immature small ribosomal subunits can engage in translation initiation in Saccharomyces cerevisiae.不成熟的小核糖体亚基可在酿酒酵母中参与翻译起始。
EMBO J. 2010 Jan 6;29(1):80-92. doi: 10.1038/emboj.2009.307. Epub 2009 Nov 5.
6
A convergence of rRNA and mRNA quality control pathways revealed by mechanistic analysis of nonfunctional rRNA decay.通过对无功能rRNA衰变的机制分析揭示的rRNA和mRNA质量控制途径的趋同。
Mol Cell. 2009 May 14;34(4):440-50. doi: 10.1016/j.molcel.2009.04.017.
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Analysis of Dom34 and its function in no-go decay.Dom34分析及其在无义衰变中的功能。
Mol Biol Cell. 2009 Jul;20(13):3025-32. doi: 10.1091/mbc.e09-01-0028. Epub 2009 May 6.
8
Single-RNA counting reveals alternative modes of gene expression in yeast.单RNA计数揭示酵母基因表达的替代模式。
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9
Coupling of ribosomal L1 stalk and tRNA dynamics during translation elongation.翻译延伸过程中核糖体L1柄与tRNA动态变化的偶联
Mol Cell. 2008 May 9;30(3):348-59. doi: 10.1016/j.molcel.2008.03.012.
10
Defining genetic interaction.定义基因相互作用。
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为什么 Dom34 会刺激 40S 核糖体亚基生物合成缺陷细胞的生长。

Why Dom34 stimulates growth of cells with defects of 40S ribosomal subunit biosynthesis.

机构信息

Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Avenue, Bronx, NY 10461, USA.

出版信息

Mol Cell Biol. 2010 Dec;30(23):5562-71. doi: 10.1128/MCB.00618-10. Epub 2010 Sep 27.

DOI:10.1128/MCB.00618-10
PMID:20876302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2976434/
Abstract

A set of genome-wide screens for proteins whose absence exacerbates growth defects due to pseudo-haploinsufficiency of ribosomal proteins in Saccharomyces cerevisiae identified Dom34 as being particularly important for cell growth when there is a deficit of 40S ribosomal subunits. In contrast, strains with a deficit of 60S ribosomal proteins were largely insensitive to the loss of Dom34. The slow growth of cells lacking Dom34 and haploinsufficient for a protein of the 40S subunit is caused by a severe shortage of 40S subunits available for translation initiation due to a combination of three effects: (i) the natural deficiency of 40S subunits due to defective synthesis, (ii) the sequestration of 40S subunits due to the large accumulation of free 60S subunits, and (iii) the accumulation of ribosomes "stuck" in a distinct 80S form, insensitive to the Mg(2+) concentration, and at least temporarily unavailable for further translation. Our data suggest that these stuck ribosomes have neither mRNA nor tRNA. We postulate, based on our results and on previously published work, that the stuck ribosomes arise because of the lack of Dom34, which normally resolves a ribosome stalled due to insufficient tRNAs, to structural problems with its mRNA, or to a defect in the ribosome itself.

摘要

一组针对蛋白质的全基因组筛选,这些蛋白质的缺失会加剧由于酿酒酵母核糖体蛋白的假单倍不足导致的生长缺陷,结果发现 Dom34 在 40S 核糖体亚基缺乏时对细胞生长特别重要。相比之下,60S 核糖体蛋白缺乏的菌株对 Dom34 的缺失基本上不敏感。由于三种效应的结合,缺乏 Dom34 和单倍不足的 40S 亚基蛋白的细胞生长缓慢:(i)由于合成缺陷导致 40S 亚基的天然缺乏,(ii)由于游离 60S 亚基的大量积累导致 40S 亚基的隔离,以及(iii)核糖体“卡住”在独特的 80S 形式中,对镁离子浓度不敏感,并且至少暂时无法进一步翻译。我们的数据表明,这些卡住的核糖体既没有 mRNA 也没有 tRNA。根据我们的结果和以前发表的工作,我们推测这些卡住的核糖体是由于缺乏 Dom34 引起的,Dom34 通常可以解决由于 tRNA 不足、其 mRNA 的结构问题或核糖体本身的缺陷而导致的核糖体停滞。