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RNA聚合酶合成的自体及转录后调控。

Autogenous and post-transcriptional regulation of RNA polymerase synthesis.

作者信息

Ishihama A, Fukuda R

出版信息

Mol Cell Biochem. 1980 Aug 16;31(3):177-96. doi: 10.1007/BF00225850.

Abstract

The regulation of gene expression was studied, for the Escherichia coli rpoBC operon, which includes the genes, rpoB and rpoC, for the beta and beta subunits of RNA polymerase, and rplJ and rplL, for the two proteins, L10 and L7/12, of the 50S ribosome. The gene organization agrees well with the accumulated observations indicating the coordinate synthesis of RNA polymerase and ribosomes under various growth conditions for wild-type E. coli cells. On the other hand, the differential regulation of the two essential components observed under restrictive growth conditions, after addition of various drugs or with certain mutants, in particular those carrying mutations in the RNA polymerase genes, was found to take place through two novel regulation systems: The transcriptional termination at an internal attenuation site and the two autogenous and posttranscriptional controls, being specific for the two ribosomal protein genes and the two RNA polymerase subunit genes, respectively. The majority of the transcription initiated from the promoter rpoP beta terminates at an attenuator site between the promoter-proximal rplJL and the promoter-distal rpoBC genes. The frequency of the attenuation seems to control the relative level of RNA polymerase synthesis to that of ribosomes. The expression of rpoBC genes is subject to an autogenous regulation, in which both RNA polymerase holoenzyme and alpha 2 beta complex function as regulatory molecules with repressor activity. The autogenous regulation was found to operate at post-transcriptional step(s), probably at the level of translation. During the study on the regulation of RNA polymerase synthesis, we noticed that the rpoBC operon contained another autogenous regulation circuit, in which the synthesis of L10 and L7/12 was specifically repressed by the L10-L7/12 complex. Molecular mechanisms and physiological meanings of the novel regulations are discussed.

摘要

对大肠杆菌rpoBC操纵子的基因表达调控进行了研究,该操纵子包含编码RNA聚合酶β亚基和β'亚基的rpoB和rpoC基因,以及编码50S核糖体的两种蛋白质L10和L7/12的rplJ和rplL基因。这种基因组织与累积的观察结果非常吻合,这些观察结果表明野生型大肠杆菌细胞在各种生长条件下RNA聚合酶和核糖体是协同合成的。另一方面,发现在限制性生长条件下,添加各种药物后或在某些突变体中,特别是那些携带RNA聚合酶基因突变的突变体中,对这两种必需成分的差异调控是通过两种新的调控系统进行的:在内部衰减位点的转录终止以及两种自体和转录后调控,分别对两种核糖体蛋白基因和两种RNA聚合酶亚基基因具有特异性。从启动子rpoPβ起始的大部分转录在启动子近端的rplJL和启动子远端的rpoBC基因之间的衰减位点处终止。衰减频率似乎控制着RNA聚合酶合成与核糖体合成的相对水平。rpoBC基因的表达受到自体调控,其中RNA聚合酶全酶和α2β复合物均作为具有阻遏活性的调控分子发挥作用。发现自体调控在转录后步骤起作用,可能在翻译水平。在研究RNA聚合酶合成的调控过程中,我们注意到rpoBC操纵子包含另一个自体调控回路,其中L10-L7/12复合物特异性抑制L10和L7/12的合成。讨论了这些新调控的分子机制和生理意义。

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