...
首页> 外文期刊>Virology >Hyperacetylation and differential deacetylation of histones H4 and H3 define two distinct classes of acetylated SV40 chromosomes early in infection
【24h】

Hyperacetylation and differential deacetylation of histones H4 and H3 define two distinct classes of acetylated SV40 chromosomes early in infection

机译:组蛋白H4和H3的过度乙酰化和差异脱乙酰化定义了感染初期的两类不同的乙酰化SV40染色体

获取原文
获取原文并翻译 | 示例
           

摘要

SV40 chromosomes undergoing encapsidation late in infection and SV40 chromatin in virions are hyperacetylated on histones H4 and H3. However, the fate of the SV40 chromosomes containing hyperacetylated histones in a subsequent round of infection has not been determined. In order to determine if SV40 chromosomes undergo changes in the extent of histone acetylation during early infection, we have analyzed SV40 chromosomes isolated 30 min and 3 h postinfection by quantitative ChIP assays, depletion ChIP assays, competitive ChIP assays, and ChIP assays combined with restriction endonuclease sensitivity using antibodies to hyperacetylated histones H4 and H3. We have shown that at 30 min postinfection, the hyperacetylated histones are associated with two distinct classes of SV40 chromosomes. One form is hyperacetylated specifically on histone H4 while a second form is hyperacetylated on both H4 and H3. Both forms of chromosomes appear to contain a nucleosome-free promoter region. Over the course of the next few hours of infection, the class of SV40 chromosomes hyperacetylated on only H4 is reduced or completely eliminated through deacetylation.
机译:在组蛋白H4和H3上,感染后期进行衣壳化的SV40染色体和病毒粒子中的SV40染色质被高度乙酰化。但是,尚未确定在随后的感染中含有超乙酰化组蛋白的SV40染色体的命运。为了确定SV40染色体在早期感染期间是否发生组蛋白乙酰化程度的变化,我们通过定量ChIP测定,耗尽ChIP测定,竞争性ChIP测定以及结合限制的ChIP测定分析了感染后30分钟和3小时分离的SV40染色体内切核酸酶敏感性使用针对超乙酰化组蛋白H4和H3的抗体。我们已经证明,在感染后30分钟,超乙酰化的组蛋白与SV40染色体的两个不同类别相关。一种形式在组蛋白H4上特异地被高度乙酰化,而第二种形式在H4和H3上都被高乙酰化。两种形式的染色体似乎都包含无核小体的启动子区域。在接下来的几个小时的感染过程中,仅H4上高度乙酰化的SV40染色体类别通过脱乙酰化而减少或完全消除。

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