Horikoshi M, Sekimizu K, Hirashima S, Mitsuhashi Y, Natori S
J Biol Chem. 1985 May 10;260(9):5739-44.
The structural relationships of S-II, S-II', and S-I(b) stimulatory proteins of RNA polymerase II purified from Ehrlich ascites tumor cells were investigated. From analysis of the amino acid compositions and tryptic peptide maps of these proteins labeled with radioiodinated Bolton-Hunter reagent, it was concluded that S-I(b) is a part of S-II located at either the amino- or carboxyl-terminal and that only this region mainly contains radioiodinatable amino acid residues when labeled using 125I. On chymotryptic digestion, S-II was cleaved to 21- and 18-kDa fragments in the presence of DNA. The 21-kDa fragment was found to be sufficient for stimulation of RNA polymerase II. It was suggested that S-II' is formed by phosphorylation of S-II in the domain containing the 18-kDa fragment.
对从艾氏腹水瘤细胞中纯化的RNA聚合酶II的S-II、S-II'和S-I(b)刺激蛋白的结构关系进行了研究。通过分析用放射性碘化博尔顿-亨特试剂标记的这些蛋白的氨基酸组成和胰蛋白酶肽图,得出结论:S-I(b)是位于氨基端或羧基端的S-II的一部分,并且在用125I标记时,只有该区域主要含有可放射性碘化的氨基酸残基。在胰凝乳蛋白酶消化时,在DNA存在下,S-II被切割成21 kDa和18 kDa的片段。发现21 kDa的片段足以刺激RNA聚合酶II。有人提出,S-II'是由S-II在含有18 kDa片段的结构域中磷酸化形成的。