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Rpb4是RNA聚合酶II的一个亚基,它能使该酶在体外极端温度下进行转录。

Rpb4, a subunit of RNA polymerase II, enables the enzyme to transcribe at temperature extremes in vitro.

作者信息

Rosenheck S, Choder M

机构信息

Department of Molecular Microbiology and Biotechnology, Faculty of Life Sciences, Tel-Aviv University, Tel-Aviv 69978, Israel.

出版信息

J Bacteriol. 1998 Dec;180(23):6187-92. doi: 10.1128/JB.180.23.6187-6192.1998.

Abstract

Rpb4 is a subunit of Saccharomyces cerevisiae RNA polymerase II (Pol II). It associates with the polymerase preferentially in stationary phase and is essential for some stress responses. Using the promoter-independent initiation and chain elongation assay, we monitored Pol II enzymatic activity in cell extracts. We show here that Rpb4 is required for the polymerase activity at temperature extremes (10 and 35 degreesC). In contrast, at moderate temperature (23 degreesC) Pol II activity is independent of Rpb4. These results are consistent with the role previously attributed to Rpb4 as a subunit whose association with Pol II helps Pol II to transcribe during extreme temperatures. The enzymatic inactivation of Pol II lacking Rpb4 at the nonoptimal temperature was prevented by the addition of recombinant Rpb4 produced in Escherichia coli prior to the in vitro reaction assay. This finding suggests that modification of Rpb4 is not required for its functional association with the other Pol II subunits. Sucrose gradient and immunoprecipitation experiments demonstrated that Rpb4 is present in the cell in excess over the Pol II complex during all growth phases. Nevertheless, the rescue of Pol II activity at the nonoptimal temperature by Rpb4 is possible only when cell extracts are obtained from postlogarithmic cells, not from logarithmically growing cells. This result suggests that Pol II molecules should be modified in order to recruit Rpb4; the portion of the modified Pol II molecules is small during logarithmic phase and becomes predominant in stationary phase.

摘要

Rpb4是酿酒酵母RNA聚合酶II(Pol II)的一个亚基。它在稳定期优先与聚合酶结合,并且对某些应激反应至关重要。利用不依赖启动子的起始和链延伸分析,我们监测了细胞提取物中的Pol II酶活性。我们在此表明,在极端温度(10和35摄氏度)下,聚合酶活性需要Rpb4。相比之下,在适中温度(23摄氏度)下,Pol II活性不依赖于Rpb4。这些结果与之前赋予Rpb4的作为一个亚基的作用一致,其与Pol II的结合有助于Pol II在极端温度下进行转录。在体外反应分析之前,通过添加在大肠杆菌中产生的重组Rpb4,可防止在非最适温度下缺乏Rpb4的Pol II的酶失活。这一发现表明,Rpb4与其他Pol II亚基的功能结合不需要对其进行修饰。蔗糖梯度和免疫沉淀实验表明,在所有生长阶段,细胞中Rpb4的含量都超过Pol II复合物。然而,只有当细胞提取物取自对数后期细胞而非对数生长期细胞时,Rpb4才有可能在非最适温度下挽救Pol II活性。这一结果表明,为了招募Rpb4,Pol II分子应该被修饰;在对数期,被修饰的Pol II分子比例较小,而在稳定期则占主导地位。

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