首页> 外文期刊>Eukaryotic cell >Class I Histone Deacetylase Thd1p Promotes Global Chromatin Condensation in Tetrahymena thermophila
【24h】

Class I Histone Deacetylase Thd1p Promotes Global Chromatin Condensation in Tetrahymena thermophila

机译:I类组蛋白去乙酰化酶Thd1p促进嗜热四膜虫的整体染色质浓缩

获取原文
           

摘要

Class I histone deacetylases (HDACs) regulate DNA-templated processes such as transcription. They act both at specific loci and more generally across global chromatin, contributing to acetylation patterns that may underlie large-scale chromatin dynamics. Although hypoacetylation is correlated with highly condensed chromatin, little is known about the contribution of individual HDACs to chromatin condensation mechanisms. Using the ciliated protozoan Tetrahymena thermophila, we investigated the role of a specific class I HDAC, Τhd1p, in the reversible condensation of global chromatin. In this system, the normal physiological response to cell starvation includes the widespread condensation of the macronuclear chromatin and general repression of gene transcription. We show that the chromatin in Thd1p-deficient cells failed to condense during starvation. The condensation failure correlated with aberrant hyperphosphorylation of histone H1 and the overexpression of CDC2, encoding the major histone H1 kinase. Changes in the rate of acetate turnover on core histones and in the distribution of acetylated lysines 9 and 23/27 on histone H3 isoforms that were found to correlate with normal chromatin condensation were absent from Thd1p mutant cells. These results point to a role for a class I HDAC in the formation of reversible higher-order chromatin structures and global genome compaction through mechanisms involving the regulation of H1 phosphorylation and core histone acetylation/deacetylation kinetics.
机译:I类组蛋白脱乙酰基酶(HDAC)调节DNA模板化的过程,例如转录。它们不仅作用于特定基因座,而且作用于整个染色质,更普遍地起作用,这可能是构成大规模染色质动力学基础的乙酰化模式。尽管低乙酰化与高度浓缩的染色质相关,但对于单个HDAC对染色质浓缩机制的贡献知之甚少。我们使用纤毛的原生动物嗜热四膜虫,研究了特定的I类HDAC Thd1p在可逆的整体染色质凝聚中的作用。在该系统中,对细胞饥饿的正常生理反应包括大核染色质的广泛凝缩和基因转录的普遍抑制。我们表明,在饥饿期间,Thd1p缺陷细胞中的染色质无法凝结。缩合失败与组蛋白H1异常的过度磷酸化和 CDC2 的过度表达有关,编码主要的组蛋白H1激酶。 Thd1p突变细胞不存在核心组蛋白上的乙酸酯转换速率的变化以及组蛋白H3亚型上乙酰化赖氨酸9和23/27的分布,这些蛋白与正常的染色质浓缩相关。这些结果表明,I类HDAC通过涉及H1磷酸化和核心组蛋白乙酰化/脱乙酰化动力学调节的机制,在可逆的高级染色质结构的形成和整体基因组紧缩中发挥作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号