曲古抑菌素A
组蛋白脱乙酰基酶2
组蛋白脱乙酰基酶
组蛋白脱乙酰基酶5
HDAC11型
HDAC4型
心理压抑
HDAC1型
癌症研究
组蛋白脱乙酰酶抑制剂
抄写(语言学)
分子生物学
HDAC10型
化学
组蛋白
生物
遗传学
基因
基因表达
哲学
语言学
作者
Ursula Vinatzer,Jan Taplick,Christian Seiser,Christa Fonatsch,Rotraud Wieser
标识
DOI:10.1046/j.1365-2141.2001.02987.x
摘要
EVI‐1 and its variant form, MDS1/EVI1, have been reported to act in an antagonistic manner and be differentially regulated in samples from patients with acute myeloid leukaemia and rearrangements of the long arm of chromosome 3. Here, we show that both EVI‐1 and MDS1/EVI1 can repress transcription from a reporter construct containing EVI‐1 binding sites and interact with histone deacetylase in mammalian cells. This interaction can be recapitulated in vitro and is mediated by a previously characterized transcription repression domain, whose activity is alleviated by the histone deacetylase inhibitor trichostatin A.
科研通智能强力驱动
Strongly Powered by AbleSci AI