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PMID: 9228069 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Tyrosine phosphorylation of RNA polymerase II carboxyl-terminal domain by the Abl-related gene product.

The Journal of biological chemistry ·Vol. 272 ·No. 30 ·1997-07-25 ·Pages 18905-9

Baskaran R, Chiang GG, Mysliwiec T, Kruh GD, Wang JY

Abstract

The largest subunit of RNA polymerase II contains a C-terminal repeated domain (CTD) that is the site of phosphorylation by serine (threonine) and tyrosine kinases. Phosphorylation of the CTD is correlated with transcription elongation. A number of different kinases have previously been shown to phosphorylate the CTD; among them is a nuclear tyrosine kinase encoded by the c-abl proto-oncogene. The processive and high stoichiometric phosphorylation of RNA polymerase II by c-Abl requires the tyrosine kinase, the SH2 domain, and a CTD-interacting domain (CTD-ID) in the Abl protein. The physiological tyrosine phosphorylation of RNA polymerase II by c-Abl in DNA damage response has previously been demonstrated. Basal tyrosine phosphorylation of RNA polymerase II, however, is observed in cells derived from abl-deficient mice, indicating the existence of other CTD tyrosine kinases. In this report, we show that the tyrosine kinase encoded by an Abl-related gene (Arg) also phosphorylates the CTD in vitro and in transfected cells. The SH2 and kinase domain of Arg are 95% identical to that of c-Abl. However, these two proteins share only 29% identity in the large C-terminal region. Interestingly, a CTD-ID is also found in the C-terminal region of Arg. Mapping studies and sequence analysis have led to the identification of the CTD-ID that is highly conserved among the divergent C-terminal regions of Abl and Arg. These results indicate that tyrosine phosphorylation of RNA polymerase II CTD could be catalyzed by either c-Abl or Arg kinase.

MeSH Terms
Amino Acid Sequence Animals Binding Sites COS Cells CSK Tyrosine-Protein Kinase Conserved Sequence Humans Mice Molecular Sequence Data Peptide Fragments/metabolism Phosphorylation Protein Kinases/metabolism Protein-Tyrosine Kinases/chemistry,metabolism Proto-Oncogene Mas Proto-Oncogene Proteins c-abl/metabolism RNA Polymerase II/metabolism Tyrosine/metabolism src Homology Domains src-Family Kinases
Chemicals
MAS1 protein, human Peptide Fragments Proto-Oncogene Mas Tyrosine Protein Kinases carboxy-terminal domain kinase Protein-Tyrosine Kinases CSK Tyrosine-Protein Kinase Proto-Oncogene Proteins c-abl src-Family Kinases CSK protein, human RNA Polymerase II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Baskaran R
Department of Biology and Center for Molecular Genetics, University of California at San Diego, La Jolla, California, 92093-0322, USA.
Chiang G G
Mysliwiec T
Kruh G D
Wang J Y
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1997-07-25
Pages
18905-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · R01 CA043054 · United States
NCI NIH HHS · R37 CA043054 · United States
NCI NIH HHS · CA-43054 · United States
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