Caron P R, Watt P, Wang J C
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Mol Cell Biol. 1994 May;14(5):3197-207. doi: 10.1128/mcb.14.5.3197-3207.1994.
A set of carboxy-terminal deletion mutants of Saccharomyces cerevisiae DNA topoisomerase II were constructed for studying the functions of the carboxyl domain in vitro and in vivo. The wild-type yeast enzyme is a homodimer with 1,429 amino acid residues in each of the two polypeptides; truncation of the C terminus to Ile-1220 has little effect on the function of the enzyme in vitro or in vivo, whereas truncations extending beyond Gln-1138 yield completely inactive proteins. Several mutant enzymes with C termini in between these two residues were found to be catalytically active but unable to complement a top2-4 temperature-sensitive mutation. Immunomicroscopy results suggest that the removal of a nuclear localization signal in the C-terminal domain is likely to contribute to the physiological dysfunction of these proteins; the ability of these mutant proteins to relax supercoiled DNA in vivo shows, however, that at least some of the mutant proteins are present in the nuclei in a catalytically active form. In contrast to the ability of the catalytically active mutant proteins to relax supercoiled intracellular DNA, all mutants that do not complement the temperature-dependent lethality and high frequency of chromosomal nondisjunction of top2-4 were found to lack decatenation activity in vivo. The plausible roles of the DNA topoisomerase II C-terminal domain, in addition to providing a signal for nuclear localization, are discussed in the light of these results.
构建了一组酿酒酵母DNA拓扑异构酶II的羧基末端缺失突变体,用于在体外和体内研究羧基结构域的功能。野生型酵母酶是一种同型二聚体,两条多肽链中每条都有1429个氨基酸残基;将C末端截短至Ile-1220对该酶在体外或体内的功能影响很小,而延伸超过Gln-1138的截短则产生完全无活性的蛋白质。发现几个C末端在这两个残基之间的突变酶具有催化活性,但无法互补top2-4温度敏感突变。免疫显微镜结果表明,C末端结构域中核定位信号的去除可能导致这些蛋白质的生理功能障碍;然而,这些突变蛋白在体内松弛超螺旋DNA的能力表明,至少一些突变蛋白以催化活性形式存在于细胞核中。与具有催化活性的突变蛋白松弛细胞内超螺旋DNA的能力相反,所有不能互补top2-4温度依赖性致死率和高频率染色体不分离的突变体在体内均缺乏解连环活性。根据这些结果,讨论了DNA拓扑异构酶II C末端结构域除了提供核定位信号外的可能作用。