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Isolation and characterization of cDNA encoding mouse RNA polymerase II subunit RPB14.

作者信息

Nishi Y, Yamamoto K, Yao Y, Yamamoto M, Nogi Y, Matsuo H, Muramatsu M

机构信息

Department of Biochemistry, Saitama Medical School, Iruma-gun, Japan.

出版信息

Gene. 1997 Mar 18;187(2):165-70. doi: 10.1016/s0378-1119(96)00739-1.

Abstract

By means of the yeast two-hybrid system using the 40-kDa subunit of mouse RNA polymerase I, mRPA40, as the bait, we isolated a mouse cDNA which encoded a protein with significant homology in amino acid sequence to the 12.5-kDa subunit of Saccharomyces cerevisiae RNA polymerase II, B12.5 (RPB11). Specific antibody raised against the recombinant protein that was derived from the cDNA reacted with a 14-kDa polypeptide in highly purified mammalian RNA polymerase II and did not react with any subunit of RNA polymerase I or III. Moreover, the antibody co-immunoprecipitated the largest subunit of mouse RNA polymerase II. These results provide biochemical evidence that the cDNA isolated, named mRPB14, encodes a specific subunit of RNA polymerase II, and indicate that the subunit organization of the enzyme is conserved between yeast and mouse. A possible role of the alpha-motif [Dequard-Chablat, M., Riva, M., Carles, C. and Sentenac, A., J. Biol. Chem. 266 (1991) 15300-15307] in the protein-protein interaction between mRPA40 and mRPB14 is also discussed.

摘要

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