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一组T7 RNA聚合酶活性位点突变体的表征

Characterization of a set of T7 RNA polymerase active site mutants.

作者信息

Bonner G, Lafer E M, Sousa R

机构信息

Department of Biochemistry, University of Texas Health Sciences Center, San Antonio 78284-7819.

出版信息

J Biol Chem. 1994 Oct 7;269(40):25120-8.

PMID:7929200
Abstract

We have evaluated the elongation rates, processivities, and abortive transcription characteristics of a set of T7 RNA polymerase mutants that map to the polymerase active site. The effects of these mutations on transcription are complex: they cause decreases in activity and processivity during both the processive and abortive phases of transcription and exhibit disproportionate decreases in activity and processivity on poly(dA).poly(dT) or poly(dT) versus poly(dG).poly(dC) templates. They also exhibit an increase in the proportion of slippage dependent poly(G) transcript synthesis during the initial stages of transcription. It is shown that these multiple, distinct effects on transcription can be attributed to decreases in the mutant enzymes' phosphodiester bond formation rates. Estimates of the decreases in these rates are derived from the measured transcript elongation rates and processivities of the mutant enzymes.

摘要

我们评估了一组定位于聚合酶活性位点的T7 RNA聚合酶突变体的延伸速率、持续合成能力和流产转录特征。这些突变对转录的影响很复杂:它们在转录的持续合成阶段和流产阶段都会导致活性和持续合成能力下降,并且在聚(dA)·聚(dT)或聚(dT)与聚(dG)·聚(dC)模板上表现出活性和持续合成能力不成比例的下降。它们在转录初始阶段还表现出依赖滑动的聚(G)转录本合成比例增加。结果表明,这些对转录的多种不同影响可归因于突变酶磷酸二酯键形成速率的降低。这些速率降低的估计值来自于测量的突变酶转录延伸速率和持续合成能力。

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