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基因dicB的鉴定与序列:来自同相位内部起始的分裂抑制剂的翻译

Identification and sequence of gene dicB: translation of the division inhibitor from an in-phase internal start.

作者信息

Cam K, Béjar S, Gil D, Bouché J P

机构信息

Centre de Recherches de Biochimie et de Génétique Cellulaires du CNRS, Toulouse, France.

出版信息

Nucleic Acids Res. 1988 Jul 25;16(14A):6327-38. doi: 10.1093/nar/16.14.6327.

Abstract

The dicA1 mutation, located in the replication termination region of Escherichia coli at 34.9 min, confers a temperature-sensitive, division defective phenotype to its hosts. Previous analysis had suggested that dicA codes for a repressor of a nearby division inhibition gene dicB. We show now that gene dicB is part of a complex operon. Five open reading frames (ORFs 1 to 5) preceeded by a promoter sensitive to dicA repression are found within a 1500 bp segment, and are organized into two clusters separated by a long untranslated region. Evidence for expression of these ORFs was obtained from in vitro or in vivo translation of plasmid-coded genes. IPTG-dependent cell filamentation was obtained when either the entire or the C-terminal part of the fourth ORF was placed under control of the lac promoter. In both cases, a 7 KD protein corresponding to translation from an in-frame ATG of ORF4 (dicB) was made. We propose that this C-terminal protein is the division inhibitor synthesized in dicA1 mutants.

摘要

dicA1突变位于大肠杆菌复制终止区34.9分钟处,赋予宿主温度敏感的分裂缺陷表型。先前的分析表明,dicA编码附近的分裂抑制基因dicB的阻遏物。我们现在表明,基因dicB是一个复杂操纵子的一部分。在一个1500 bp的片段内发现了五个开放阅读框(ORF1至5),其前面有一个对dicA阻遏敏感的启动子,并被组织成两个由长非翻译区隔开的簇。这些ORF表达的证据来自质粒编码基因的体外或体内翻译。当第四个ORF的全部或C末端部分置于lac启动子控制下时,可获得IPTG依赖性细胞丝化。在这两种情况下,都产生了一种7 KD的蛋白质,对应于从ORF4(dicB)的框内ATG翻译而来。我们提出,这种C末端蛋白质是在dicA1突变体中合成的分裂抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b15/338298/49084325700b/nar00167-0080-a.jpg

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