Trimethylated lysine 9 of histone H3 is a mark for DNA methylation in Neurospora crassa

被引:0
|
作者
Hisashi Tamaru
Xing Zhang
Debra McMillen
Prim B. Singh
Jun-ichi Nakayama
Shiv I. Grewal
C. David Allis
Xiaodong Cheng
Eric U. Selker
机构
[1] Institute of Molecular Biology,Department of Biochemistry
[2] University of Oregon,Division of Gene Expression and Development
[3] Emory University School of Medicine,Department of Biochemistry and Molecular Genetics
[4] Nuclear Reprogramming Laboratory,Laboratory for Chromatin Dynamics, Center for Developmental Biology
[5] The Roslin Institute,undefined
[6] Cold Spring Harbor Laboratory,undefined
[7] University of Virginia Health Sciences Center,undefined
[8] RIKEN,undefined
来源
Nature Genetics | 2003年 / 34卷
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摘要
Besides serving to package nuclear DNA, histones carry information in the form of a diverse array of post-translational modifications. Methylation of histones H3 and H4 has been implicated in long-term epigenetic 'memory'1. Dimethylation or trimethylation of Lys4 of histone H3 (H3 Lys4) has been found in expressible euchromatin of yeasts and mammals2,3,4. In contrast, methylation of Lys9 of histone H3 (H3 Lys9) has been implicated in establishing and maintaining the largely quiescent heterochromatin of mammals, yeasts, Drosophila melanogaster and plants5,6,7,8,9. We have previously shown that a DNA methylation mutant of Neurospora crassa, dim-5 (defective in methylation), has a nonsense mutation in the SET domain of an H3-specific histone methyltransferase and that substitutions of H3 Lys9 cause gross hypomethylation of DNA10. Similarly, the KRYPTONITE histone methyltransferase is required for full DNA methylation in Arabidopsis thaliana11. We used biochemical, genetic and immunological methods to investigate the specific mark for DNA methylation in N. crassa. Here we show that trimethylated H3 Lys9, but not dimethylated H3 Lys9, marks chromatin regions for cytosine methylation and that DIM-5 specifically creates this mark.
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页码:75 / 79
页数:4
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