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大肠杆菌核糖体蛋白L12的DNA依赖性合成的体外调控

In vitro regulation of DNA-dependent synthesis of Escherichia coli ribosomal protein L12.

作者信息

Goldberg G, Caldwell P, Weissbach H, Brot N

出版信息

Proc Natl Acad Sci U S A. 1979 Apr;76(4):1716-20. doi: 10.1073/pnas.76.4.1716.

Abstract

The DNA of the transducing phage lambdarifd18 contains, among others, the genes for the ribosomal proteins L11, L1, L10, and L12 and the beta and beta' subunits of RNA polymerase (nucleosidetriphosphate:RNA nucleotidyltransferase, EC 2.7.7.6). In a coupled in vitro protein-synthesis system, lambdarifd18 DNA directs the synthesis of about four to five molecules of L12 per molecule of L10. This is consistent with the finding that there are four copies of L12 per ribosome. The ratio of L12/L10 was also examined from an EcoRI fragment of lambdarifd18 that contains the L10 gene and about 50% of the L12 gene. A significantly lower ratio of truncated L12/L10 was observed compared to the intact phage. The binding of RNA polymerase to various lambdarifd18 DNA restriction fragments was used to locate possible promoter sites. These binding experiments suggest that the beta and beta' subunits of RNA polymerase are cotranscribed with at least ribosomal protein L12 and, also, that there may be an additional promoter site for the L12 gene within the structural gene for L10.

摘要

转导噬菌体λrifd18的DNA中,除其他基因外,还包含核糖体蛋白L11、L1、L10和L12以及RNA聚合酶β和β'亚基(核苷三磷酸:RNA核苷酸转移酶,EC 2.7.7.6)的基因。在一个体外偶联蛋白质合成系统中,λrifd18 DNA指导每分子L10合成约四到五个分子的L12。这与每个核糖体有四个L12拷贝的发现一致。还从λrifd18的一个包含L10基因和约50%的L12基因的EcoRI片段中检测了L12/L10的比例。与完整噬菌体相比,观察到截短的L12/L10比例明显较低。利用RNA聚合酶与各种λrifd18 DNA限制片段的结合来定位可能的启动子位点。这些结合实验表明,RNA聚合酶的β和β'亚基至少与核糖体蛋白L12共转录,并且在L10的结构基因内可能存在L12基因的另一个启动子位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fea/383461/be2234cdffd9/pnas00004-0201-a.jpg

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