A novel EID-1 family member, EID-2, associates with histone deacetylases and inhibits muscle differentiation

A novel EID-1 family member, EID-2, associates with histone deacetylases and inhibits muscle differentiation
复制标题

DOI:
10.1074/jbc.m212212200
复制
发表时间:
2003-05-09
影响因子:
4.8
通讯作者:
Yuasa, Y
Yuasa, Y
中科院分区:
生物学2区
文献类型:
--
作者:
Miyake, S;Yanagisawa, Y;Yuasa, Y

文献摘要

被引文献

相似文献

EID-1((E)在条1A下-样(i)在条1A下-样(d)在条1A下-样(1)在条1A下-样(i)在条1A下-样(1)在条1A下-样(d)在条1A下-样(1)在条1A下-样(i)在条1A下-样(1)在条1A下-样(d)在条1A下-样(1)在条1A下-样(1)在条1A下-样抑制剂)通过阻断p300的组蛋白乙酰转移酶活性来抑制分化。在这里,我们报告了一种新的分化抑制剂,表现出与EID-1的同源性,称为EID-2((E)在bar ID-1下-样(i)在bar抑制剂下(d)在bar分化下-(2)在bar下)。EID-2抑制MyoD依赖性转录和肌肉分化。与EID-1不同,EID-2不阻断p300活性。有趣的是,EID-2与I类组蛋白脱乙酰酶(HDAC)相关。EID-2的N-末端部分是与HDAC结合所必需的。该区域还参与转录抑制和核定位,表明HDAC参与EID-2功能的重要性。这些结果表明一个新的分化抑制剂家族,尽管EID-2和EID-1之间的生化机制存在一些差异。
An EID-1 ((E) under bar 1A-like (i) under bar nhibitor of (d) under bar ifferentiation-(1) under bar) inhibits differentiation by blocking the histone acetyltransferase activity of p300. Here we report a novel inhibitor of differentiation exhibiting homology to EID-1, termed EID-2 ((E) under bar ID-1- like (i) under bar nhibitor of (d) under bar ifferentiation-(2) under bar). EID-2 inhibited MyoD-dependent transcription and muscle differentiation. Unlike EID-1, EID-2 did not block p300 activity. Interestingly, EID-2 associated with class I histone deacetylases (HDACs). The N-terminal portion of EID-2 was required for the binding to HDACs. This region was also involved in the transcriptional repression and nuclear localization, suggesting the importance of the involvement of HDACs in the EID-2 function. These results indicate a new family of differentiation inhibitors, although there are several differences in the biochemical mechanisms between EID-2 and EID-1.