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酵母中多核糖体的生物发生及信使核糖核酸的转运

Biogenesis of polysomes and transport of messenger RNA in yeast.

作者信息

Brañes L, Pogo A O

出版信息

Eur J Biochem. 1975 Jun;54(2):317-28. doi: 10.1111/j.1432-1033.1975.tb04142.x.

Abstract

The study of polysomal formation in the ts-136 thermo-sensitive yeast mutant indicates that ribosomes are assembled with an mRNA, which is in a structure tightly bound to membranes, and are then released into the soluble cytoplasmic fraction. This has been observed by studying the recruitment of ribosomes when glucose is added to glucose-starved cells and when transport of mRNA is permitted by shifting the mutant to the permissive temperature. A soluble cytoplasm and a fraction becoming soluble after sodium deoxycholate treatment of a rapidly sedimenting structure have been characterized. The former contains the majority of polysomes, free 80-S monomers and almost all of the ribosomal subunits. The latter fraction is composed of bound 80-S monomers and polysomes, but lacks ribosomal subunits. Treatment of the rapidly sedimenting structure with pancreatic ribonuclease produces the release of 80-S monomers, with EDTA the release of an equal proportion of both ribosomal subunits, and with sodium deoxycholate the release of 80-S monomers and polysomes. These findings are consistent with the assumption that bound ribosomes are assembled with an mRNA which is tightly bound to this rapidly sedimenting structure, presumably membranes. From the operational viewpoint this fraction is called the "membrane." During the process of polysomal formation ribosomes are recruited more rapidly in the "membranes" than in the soluble cytoplasm. Since "membranes" do not accumulate polysomes and contain only a small fraction of the total amount of ribosomes, the result is consistent with the assumption that either there is a higher turnover of bound versus free polysomes or bound polysomes are the precursors of free polysomes. The latter assumption is more likely since we have shown previously (a) that in yeast, transport is coupled with the translation of bound mRNA, (b) that this mRNA is tightly bound to a structure which sediments very rapidly and becomes soluble only after sodium deoxycholate treatment, and (c) when cycloheximide is added during the recruitment of ribosomes there is accumulation of membrane-bound ribosomes.

摘要

对ts - 136温度敏感型酵母突变体中多聚核糖体形成的研究表明,核糖体与一种mRNA组装在一起,该mRNA处于与膜紧密结合的结构中,然后释放到可溶性细胞质部分。通过研究向葡萄糖饥饿细胞中添加葡萄糖时以及将突变体转移到允许温度从而允许mRNA转运时核糖体的募集情况,观察到了这一现象。对快速沉降结构进行脱氧胆酸钠处理后,已对可溶性细胞质和一部分变为可溶性的部分进行了表征。前者包含大多数多聚核糖体、游离的80 - S单体以及几乎所有的核糖体亚基。后者部分由结合的80 - S单体和多聚核糖体组成,但缺乏核糖体亚基。用胰核糖核酸酶处理快速沉降结构会导致80 - S单体的释放,用乙二胺四乙酸(EDTA)会导致等量的两种核糖体亚基的释放,用脱氧胆酸钠会导致80 - S单体和多聚核糖体的释放。这些发现与以下假设一致,即结合核糖体与紧密结合在这种快速沉降结构(可能是膜)上的mRNA组装在一起。从操作角度来看,这一部分被称为“膜”。在多聚核糖体形成过程中,核糖体在“膜”中比在可溶性细胞质中募集得更快。由于“膜”不会积累多聚核糖体且仅包含核糖体总量的一小部分,结果与以下假设一致,即要么结合多聚核糖体与游离多聚核糖体相比有更高的周转率,要么结合多聚核糖体是游离多聚核糖体的前体。后一种假设更有可能,因为我们之前已经表明:(a)在酵母中,转运与结合mRNA的翻译偶联;(b)这种mRNA紧密结合在一个沉降非常快且仅在脱氧胆酸钠处理后才变为可溶性的结构上;(c)当在核糖体募集过程中添加环己酰亚胺时,会有膜结合核糖体的积累。

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