Giaever G N, Wang J C
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Cell. 1988 Dec 2;55(5):849-56. doi: 10.1016/0092-8674(88)90140-7.
The supercoiling of 2 micron DNA in yeast by a process or processes that generate positively and negatively supercoiled domains was shown by the use of yeast DNA topoisomerase mutants expressing Escherichia coli DNA topoisomerase I, an enzyme that relaxes negative supercoils specifically. Intracellular 2 micron DNA becomes positively supercoiled in yeast top1 top2 ts strains expressing the E. coli enzyme when neither one of the yeast DNA topoisomerases I and II is functional. Examination of the linking number distributions of plasmids bearing the inducible promoters of GAL1 and GAL10 genes indicates that the generation of supercoiled domains of opposite signs is related to transcription.
通过使用表达大肠杆菌DNA拓扑异构酶I(一种特异性松弛负超螺旋的酶)的酵母DNA拓扑异构酶突变体,研究表明酵母中2微米DNA通过产生正超螺旋和负超螺旋结构域的一个或多个过程发生超螺旋化。当酵母DNA拓扑异构酶I和II均无功能时,在表达大肠杆菌酶的酵母top1 top2 ts菌株中,细胞内2微米DNA会变成正超螺旋。对携带GAL1和GAL10基因诱导型启动子的质粒的连环数分布进行检测表明,相反符号超螺旋结构域的产生与转录有关。