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不同细菌中的释放因子2移码位点。

Release factor 2 frameshifting sites in different bacteria.

作者信息

Baranov Pavel V, Gesteland Raymond F, Atkins John F

机构信息

Department of Human Genetics, University of Utah, 15N 2030E Room 7410, Salt Lake City, UT 84112-5330, USA.

出版信息

EMBO Rep. 2002 Apr;3(4):373-7. doi: 10.1093/embo-reports/kvf065. Epub 2002 Mar 15.

Abstract

The mRNA encoding Escherichia coli polypeptide chain release factor 2 (RF2) has two partially overlapping reading frames. Synthesis of RF2 involves ribosomes shifting to the +1 reading frame at the end of the first open reading frame (ORF). Frameshifting serves an autoregulatory function. The RF2 gene sequences from the 86 additional bacterial species now available have been analyzed. Thirty percent of them have a single ORF and their expression does not require frameshifting. In the approximately 70% that utilize frameshifting, the sequence cassette responsible for frameshifting is highly conserved. In the E. coli RF2 gene, an internal Shine-Dalgarno (SD) sequence just before the shift site was shown earlier to be important for frameshifting. Mutagenic data presented here show that the spacer region between the SD sequence and the shift site influences frameshifting, and possible mechanisms are discussed. Internal translation initiation occurs at the shift site, but any functional role is obscure.

摘要

编码大肠杆菌多肽链释放因子2(RF2)的信使核糖核酸(mRNA)有两个部分重叠的阅读框。RF2的合成涉及核糖体在第一个开放阅读框(ORF)末端转移到+1阅读框。移码具有自动调节功能。现已对另外86种细菌的RF2基因序列进行了分析。其中30%有单一开放阅读框,其表达不需要移码。在约70%利用移码的细菌中,负责移码的序列盒高度保守。在大肠杆菌RF2基因中,先前已表明移码位点前的内部夏因-达尔加诺(SD)序列对移码很重要。此处给出的诱变数据表明,SD序列与移码位点之间的间隔区影响移码,并讨论了可能的机制。内部翻译起始发生在移码位点,但任何功能作用尚不清楚。

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