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PMID: 9237170 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

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

Methods (San Diego, Calif.) ·Vol. 12 ·No. 3 ·1997-07-00 ·Pages 264-75

Morris DP, Lee JM, Sterner DE, Brickey WJ, Greenleaf AL

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.

MeSH Terms
Animals Drosophila melanogaster/enzymology Phosphorylation Protein Kinases/chemistry,metabolism RNA Polymerase II/chemistry,metabolism Saccharomyces cerevisiae/enzymology
Chemicals
Protein Kinases carboxy-terminal domain kinase RNA Polymerase II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Morris D P
Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA.
Lee J M
Sterner D E
Brickey W J
Greenleaf A L
Article Info
Journal
Methods (San Diego, Calif.)
Abbr.
Methods
ISSN
1046-2023
Published
1997-07-00
Pages
264-75
Language
English
Region
United States
NLM ID
9426302
Subset
IM
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