Chi Ya-Hui, Haller Kerstin, Peloponese Jean-Marie, Jeang Kuan-Teh
Molecular Virology Section, Laboratory of Molecular Microbiology, NIAID, National Institutes of Health, Bethesda, Maryland 20892.
Molecular Virology Section, Laboratory of Molecular Microbiology, NIAID, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 2007 Sep 14;282(37):27447-27458. doi: 10.1074/jbc.M703098200. Epub 2007 Jul 13.
Replicated mammalian chromosomes condense to segregate during anaphase, and they de-condense at the conclusion of mitosis. Currently, it is not understood what the factors and events are that specify de-condensation. Here, we demonstrate that chromosome de-condensation needs the function of an inner nuclear membrane (INM) protein hsSUN1 and a membrane-associated histone acetyltransferase (HAT), hALP. We propose that nascently reforming nuclear envelope employs hsSUN1 and hALP to acetylate histones for de-compacting DNA at the end of mitosis.
复制后的哺乳动物染色体在后期凝聚以便分离,并在有丝分裂结束时解聚。目前,尚不清楚导致解聚的因素和事件是什么。在这里,我们证明染色体解聚需要内核膜(INM)蛋白hsSUN1和膜相关组蛋白乙酰转移酶(HAT)hALP的功能。我们提出,新生的核膜利用hsSUN1和hALP在有丝分裂末期使组蛋白乙酰化,从而使DNA去压缩。