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体外测定CTD激酶及体内RNA聚合酶II的磷酸化调节特性。

Assaying CTD kinases in vitro and phosphorylation-modulated properties of RNA polymerase II in vivo.

作者信息

Morris D P, Lee J M, Sterner D E, Brickey W J, Greenleaf A L

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Methods. 1997 Jul;12(3):264-75. doi: 10.1006/meth.1997.0478.

Abstract

The functional properties of RNA polymerase II are modulated by hyperphosphorylation of its unique C-terminal repeat domain (CTD). A number of enzymes with CTD kinase activity have been identified, and correlations between CTD phosphorylation and RNA polymerase II function have been made. Here we describe methods for assaying CTD kinases and for characterizing them enzymologically. In addition we present approaches for studying phosphorylation-mediated behavior of chromosome-associated RNA polymerase II by using CTD-directed, phosphorylation state-sensitive antibodies and in situ localization techniques. The methods described here should, in conjunction with genetic approaches, contribute to elucidating the physiological roles of CTD kinases.

摘要

RNA聚合酶II的功能特性通过其独特的C末端重复结构域(CTD)的过度磷酸化来调节。已鉴定出多种具有CTD激酶活性的酶,并建立了CTD磷酸化与RNA聚合酶II功能之间的相关性。在此,我们描述了检测CTD激酶并对其进行酶学表征的方法。此外,我们还介绍了通过使用CTD定向的、磷酸化状态敏感的抗体和原位定位技术来研究与染色体相关的RNA聚合酶II的磷酸化介导行为的方法。本文所述方法应与遗传学方法相结合,有助于阐明CTD激酶的生理作用。

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