Hartsuiker E, Bähler J, Kohli J
Institute of General Microbiology, University of Bern, 3012 Bern, Switzerland.
Mol Biol Cell. 1998 Oct;9(10):2739-50. doi: 10.1091/mbc.9.10.2739.
Topoisomerase II is able to break and rejoin double-strand DNA. It controls the topological state and forms and resolves knots and catenanes. Not much is known about the relation between the chromosome segregation and condensation defects as found in yeast top2 mutants and the role of topoisomerase II in meiosis. We studied meiosis in a heat-sensitive top2 mutant of Schizosaccharomyces pombe. Topoisomerase II is not required until shortly before meiosis I. The enzyme is necessary for condensation shortly before the first meiotic division but not for early meiotic prophase condensation. DNA replication, prophase morphology, and dynamics of the linear elements are normal in the top2 mutant. The top2 cells are not able to perform meiosis I. Arrested cells have four spindle pole bodies and two spindles but only one nucleus, suggesting that the arrest is nonregulatory. Finally, we show that the arrest is partly solved in a top2 rec7 double mutant, indicating that topoisomerase II functions in the segregation of recombined chromosomes. We suggest that the inability to decatenate the replicated DNA is the primary defect in top2. This leads to a loss of chromatin condensation shortly before meiosis I, failure of sister chromatid separation, and a nonregulatory arrest.
拓扑异构酶II能够切断并重新连接双链DNA。它控制拓扑状态,形成并解开结和连环体。关于酵母top2突变体中发现的染色体分离和浓缩缺陷之间的关系以及拓扑异构酶II在减数分裂中的作用,目前所知甚少。我们研究了粟酒裂殖酵母的一个热敏感top2突变体中的减数分裂。拓扑异构酶II直到减数分裂I前不久才是必需的。该酶在第一次减数分裂前不久的浓缩过程中是必需的,但对减数分裂前期早期的浓缩不是必需的。top2突变体中的DNA复制、前期形态和线性元件的动态是正常的。top2细胞无法进行减数分裂I。停滞的细胞有四个纺锤极体和两个纺锤体,但只有一个细胞核,这表明停滞是非调节性的。最后,我们表明在top2 rec7双突变体中停滞部分得到解决,这表明拓扑异构酶II在重组染色体的分离中起作用。我们认为无法解开复制的DNA是top2中的主要缺陷。这导致在减数分裂I前不久染色质浓缩丧失、姐妹染色单体分离失败以及非调节性停滞。