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与细胞增殖和染色体凝聚相关的组蛋白磷酸化的细胞周期特异性变化。

Cell cycle-specific changes in histone phosphorylation associated with cell proliferation and chromosome condensation.

作者信息

Gurley L R, Walters R A, Tobey R A

出版信息

J Cell Biol. 1974 Feb;60(2):356-64. doi: 10.1083/jcb.60.2.356.

Abstract

Preparative polyacrylamide gel electrophoresis was used to examine histone phosphorylation in synchronized Chinese hamster cells (line CHO). Results showed that histone f1 phosphorylation, absent in G(1)-arrested and early G(1)-traversing cells, commences 2 h before entry of traversing cells into the S phase. It is concluded that f1 phosphorylation is one of the earliest biochemical events associated with conversion of nonproliferating cells to proliferating cells occurring on old f1 before synthesis of new f1 during the S phase. Results also showed that f3 and a subfraction of f1 were rapidly phosphorylated only during the time when cells were crossing the G(2)/M boundary and traversing prophase. Since these phosphorylation events do not occur in G(1), S, or G(2) and are reduced greatly in metaphase, it is concluded that these two specific phosphorylation events are involved with condensation of interphase chromatin into mitotic chromosomes. This conclusion is supported by loss of prelabeled (32)PO(4) from those specific histone fractions during transition of metaphase cells into interphase G(1) cells. A model of the relationship of histone phosphorylation to the cell cycle is presented which suggests involvement of f1 phosphorylation in chromatin structural changes associated with a continuous interphase "chromosome cycle" which culminates at mitosis with an f3 and f1 phosphorylation-mediated chromosome condensation.

摘要

采用制备型聚丙烯酰胺凝胶电泳检测同步化的中国仓鼠细胞(CHO细胞系)中的组蛋白磷酸化情况。结果显示,在G1期停滞和早期穿越G1期的细胞中不存在组蛋白f1磷酸化,而在穿越G1期的细胞进入S期前2小时开始出现。得出的结论是,f1磷酸化是与非增殖细胞向增殖细胞转变相关的最早生化事件之一,发生在S期新f1合成之前的旧f1上。结果还表明,只有在细胞穿越G2/M边界并进入前期时,f3和f1的一个亚组分才会迅速磷酸化。由于这些磷酸化事件在G1期、S期或G2期不发生,且在中期大大减少,因此得出结论,这两个特定的磷酸化事件与间期染色质凝聚为有丝分裂染色体有关。中期细胞向间期G1期细胞转变过程中,那些特定组蛋白组分中预标记的(32)PO(4)丢失,支持了这一结论。本文提出了一个组蛋白磷酸化与细胞周期关系的模型,该模型表明f1磷酸化参与了与连续间期“染色体周期”相关的染色质结构变化,该周期在有丝分裂时以f3和f1磷酸化介导的染色体凝聚达到顶点。

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