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TFIIIB 组分磷酸化介导的体外 RNA 聚合酶 III 转录的有丝分裂抑制

Mitotic repression of RNA polymerase III transcription in vitro mediated by phosphorylation of a TFIIIB component.

作者信息

Gottesfeld J M, Wolf V J, Dang T, Forbes D J, Hartl P

机构信息

Department of Molecular Biology, Scripps Research Institute, La Jolla, CA 92037.

出版信息

Science. 1994 Jan 7;263(5143):81-4. doi: 10.1126/science.8272869.

Abstract

Interphase cytosol extracts prepared from Xenopus laevis eggs are active in RNA polymerase III (Pol III) transcription. Addition of recombinant B1 cyclin to these extracts activates mitotic protein kinases that repress transcription. Affinity-purified p34cdc2-cyclin B kinase (mitosis-promoting factor) is sufficient to effect this repression in a simplified Pol III transcription system. This mitotic repression involves the direct phosphorylation of a component of the Pol III transcription initiation factor TFIIIB, which consists of the TATA box-binding protein (TBP) and associated Pol III-specific factors. The transcriptional activity of the TFIIIB-TBP fraction can be modulated in vitro by phosphorylation with mitotic kinases and by dephosphorylation with immobilized alkaline phosphatase.

摘要

从非洲爪蟾卵中制备的间期胞质溶胶提取物在RNA聚合酶III(Pol III)转录中具有活性。向这些提取物中添加重组B1周期蛋白可激活抑制转录的有丝分裂蛋白激酶。亲和纯化的p34cdc2-周期蛋白B激酶(促有丝分裂因子)足以在简化的Pol III转录系统中实现这种抑制作用。这种有丝分裂抑制涉及Pol III转录起始因子TFIIIB的一个组分的直接磷酸化,TFIIIB由TATA盒结合蛋白(TBP)和相关的Pol III特异性因子组成。TFIIIB-TBP组分的转录活性可在体外通过有丝分裂激酶的磷酸化和固定化碱性磷酸酶的去磷酸化来调节。

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