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有丝分裂 DNA 的正超螺旋结构驱动真核生物中拓扑异构酶 II 的解连环。

Positive supercoiling of mitotic DNA drives decatenation by topoisomerase II in eukaryotes.

机构信息

Medical Research Council (MRC) Clinical Sciences Centre, Imperial College London, Hammersmith Hospital, London, UK.

出版信息

Science. 2011 Mar 11;331(6022):1328-32. doi: 10.1126/science.1201538.

Abstract

DNA topoisomerase II completely removes DNA intertwining, or catenation, between sister chromatids before they are segregated during cell division. How this occurs throughout the genome is poorly understood. We demonstrate that in yeast, centromeric plasmids undergo a dramatic change in their topology as the cells pass through mitosis. This change is characterized by positive supercoiling of the DNA and requires mitotic spindles and the condensin factor Smc2. When mitotic positive supercoiling occurs on decatenated DNA, it is rapidly relaxed by topoisomerase II. However, when positive supercoiling takes place in catenated plasmid, topoisomerase II activity is directed toward decatenation of the molecules before relaxation. Thus, a topological change on DNA drives topoisomerase II to decatenate molecules during mitosis, potentially driving the full decatenation of the genome.

摘要

DNA 拓扑异构酶 II 在细胞分裂过程中姐妹染色单体分离之前,完全消除 DNA 之间的缠绕或连环。目前人们对整个基因组中这一过程的了解甚少。我们证明,在酵母中,着丝粒质粒在细胞通过有丝分裂时其拓扑结构会发生剧烈变化。这种变化的特征是 DNA 的正超螺旋化,需要有丝分裂纺锤体和凝聚素因子 Smc2。当去连环的 DNA 上出现有丝分裂正超螺旋时,拓扑异构酶 II 会迅速使其松弛。然而,当连环质粒上出现正超螺旋时,拓扑异构酶 II 的活性会先指向分子的去连环化,然后再进行松弛。因此,DNA 上的拓扑变化促使拓扑异构酶 II 在有丝分裂过程中解开分子,这可能会驱动基因组的完全去连环化。

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