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噬菌体P1的immI操纵子中icd基因的克隆、表达及特性分析

Cloning, expression, and characterization of the icd gene in the immI operon of bacteriophage P1.

作者信息

Riedel H D, Heinrich J, Schuster H

机构信息

Max-Planck-Institut für Molekulare Genetik, Berlin, Germany.

出版信息

J Bacteriol. 1993 May;175(10):2833-8. doi: 10.1128/jb.175.10.2833-2838.1993.

Abstract

The immI operon of P1 contains the genes c4, icd (formerly called orfx), and ant which are constitutively transcribed in that order from a single promoter, P51b. C4 is an antisense RNA which is processed from the precursor transcript. C4 RNA acts as a translational repressor of icd, thereby also inhibiting antirepressor (ant) synthesis. We have cloned the icd and the overlapping icd and ant genes. We show, by means of plasmid deletion analysis, that icd is translationally coupled to ant. An internal in-frame deletion of icd making up 65% of the codons still allows antirepressor synthesis at a reduced rate, indicating that a functionally active icd gene product is dispensable for ant expression. We identify the product of the icd gene as a 7.3-kDa protein which interferes with cell division. The results suggest that constitutive expression of icd, in the absence of a functionally active antirepressor, prevents P1 lysogen formation because of its detrimental effect on the host cell.

摘要

噬菌体P1的immI操纵子包含基因c4、icd(以前称为orfx)和ant,它们从单个启动子P51b开始按此顺序组成型转录。C4是一种反义RNA,由前体转录本加工而来。C4 RNA作为icd的翻译阻遏物,从而也抑制抗阻遏物(ant)的合成。我们克隆了icd以及重叠的icd和ant基因。通过质粒缺失分析,我们表明icd与ant在翻译上偶联。icd的一个内部框内缺失占密码子的65%,仍然允许抗阻遏物以降低的速率合成,这表明功能性活性的icd基因产物对于ant的表达是可有可无的。我们将icd基因的产物鉴定为一种7.3 kDa的蛋白质,它干扰细胞分裂。结果表明,在没有功能性活性抗阻遏物的情况下,icd的组成型表达由于其对宿主细胞的有害作用而阻止P1溶原形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9194/204598/5a2ac8f9cbe5/jbacter00052-0054-a.jpg

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