Physical and functional association of SU(VAR)3-9 and HDAC1 in Drosophila

被引:141
作者
Czermin, B
Schotta, G
Hülsmann, BB
Brehm, A
Becker, PB
Reuter, G
Imhof, A
机构
[1] Univ Munich, Adolf Butenandt Inst, D-80336 Munich, Germany
[2] Martin Luther Univ Halle Biol, Inst Genet, D-06120 Halle Saale, Germany
关键词
D O I
10.1093/embo-reports/kve210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Modification of histones can have a dramatic impact on chromatin structure and function. Acetylation of lysines within the N-terminal tail of the histone octamer marks transcriptionally active regions of the genome whereas deacetylation seems to play a role in transcriptional silencing. Recently, the methylation of the histone tails has also been shown to be important for transcriptional regulation and chromosome structure. Here we show by immunoaffinity purification that two activities important for chromatin-mediated gene silencing, the histone methyltransferase SU(VAR)3-9 and the histone deacetylase HDAC1, associate in vivo. The two activities cooperate to methylate pre-acetylated histones. Both enzymes are modifiers of position effect variegation and interact genetically in flies. We suggest a model in which the concerted histone deacetylation and methylation by a SU(VAR)3-9/HDAC1-containing complex leads to a permanent silencing of transcription in particular areas of the genome.
引用
收藏
页码:915 / 919
页数:5
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