Kobor Michael S, Greenblatt Jack
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Biochim Biophys Acta. 2002 Sep 13;1577(2):261-275. doi: 10.1016/s0167-4781(02)00457-8.
The synthesis of mRNA by RNA polymerase II (RNAPII) is a multistep process that is regulated by different mechanisms. One important aspect of transcriptional regulation is phosphorylation of components of the transcription apparatus. The phosphorylation state of RNAPII carboxy-terminal domain (CTD) is controlled by a variety of protein kinases and at least one protein phosphatase. We discuss emerging genetic and biochemical evidence that points to a role of these factors not only in transcription initiation but also in elongation and possibly termination. In addition, we review phosphorylation events involving some of the general transcription factors (GTFs) and other regulatory proteins. As an interesting example, we describe the modulation of transcription associated kinases and phosphatase by the HIV Tat protein. We focus on bringing together recent findings and propose a revised model for the RNAPII phosphorylation cycle.
RNA聚合酶II(RNAPII)合成mRNA是一个多步骤过程,受不同机制调控。转录调控的一个重要方面是转录装置组分的磷酸化。RNAPII羧基末端结构域(CTD)的磷酸化状态由多种蛋白激酶和至少一种蛋白磷酸酶控制。我们讨论了新出现的遗传学和生化证据,这些证据表明这些因子不仅在转录起始中起作用,而且在延伸甚至可能在终止过程中也发挥作用。此外,我们综述了涉及一些通用转录因子(GTF)和其他调控蛋白的磷酸化事件。作为一个有趣的例子,我们描述了HIV Tat蛋白对转录相关激酶和磷酸酶的调节作用。我们着重整合近期的研究发现,并提出一个关于RNAPII磷酸化循环的修订模型。