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原核生物mRNA翻译所需的富含尿苷的序列。

A uridine-rich sequence required for translation of prokaryotic mRNA.

作者信息

Zhang J, Deutscher M P

机构信息

Department of Biochemistry, University of Connecticut Health Center, Farmington 06030.

出版信息

Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2605-9. doi: 10.1073/pnas.89.7.2605.

Abstract

Binding of 30S ribosomal subunits to mRNA during the initiation of prokaryotic translation is known to be influenced by the initiation codon and the Shine-Dalgarno sequence. Site-directed mutagenesis of rnd, the Escherichia coli gene encoding RNase D, has now shown that a U8 sequence upstream of the Shine-Dalgarno region is also essential for expression of this mRNA. Alteration of two to five uridine residues within this sequence has no effect on mRNA levels but decreases RNase D protein and activity by as much as 95%, indicating that the U-rich sequence acts as an enhancer of translation. Moreover, mutant transcripts bind to 30S ribosomes in vitro with lower affinity than their wild-type counterparts, suggesting that the role of the U8 sequence is in the initial binding of ribosomes to the translation initiation region of the message. These data demonstrate that sequences other than those previously recognized can be essential for translation initiation.

摘要

已知在原核生物翻译起始过程中,30S核糖体亚基与mRNA的结合受起始密码子和Shine-Dalgarno序列的影响。对编码核糖核酸酶D的大肠杆菌基因rnd进行定点诱变,现已表明Shine-Dalgarno区域上游的U8序列对该mRNA的表达也至关重要。此序列内两到五个尿苷残基的改变对mRNA水平没有影响,但会使核糖核酸酶D蛋白和活性降低多达95%,这表明富含U的序列起到翻译增强子的作用。此外,突变转录本在体外与30S核糖体结合的亲和力低于其野生型对应物,这表明U8序列的作用在于核糖体与信使RNA翻译起始区域的初始结合。这些数据表明,除了先前识别的序列外,其他序列对翻译起始也可能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a06b/48710/a638044b74d0/pnas01081-0107-a.jpg

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