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Interaction of the Arabidopsis UV-B-Specific Signaling Component UVR8 with Chromatin

Interaction of the Arabidopsis UV-B-Specific Signaling Component UVR8 with Chromatin

作     者:Catherine Cloix Gareth I. Jenkins 

作者机构:Plant Science Group Division of Biochemistry and Molecular Biology Institute of Biomedical and Life Sciences Bower Building University of GlasgowGlasgow G12 BQQ UK 

出 版 物:《Molecular Plant》 (分子植物(英文版))

年 卷 期:2008年第1卷第1期

页      面:118-128页

核心收录:

学科分类:0710[理学-生物学] 07[理学] 09[农学] 0903[农学-农业资源与环境] 071007[理学-遗传学] 090302[农学-植物营养学] 0901[农学-作物学] 090102[农学-作物遗传育种] 

基  金:Biotechnology and Biological Sciences Research Council  BBSRC  (BB/D019281/1) 

主  题:UV RESISTANCE LOCUS8 (UVR8) chromatin immunoprecipitation (ChIP) 

摘      要:Arabidopsis UV RESISTANCE LOCUS8 (UVR8) is a UV-B-specific signaling component that regulates expression of a range of genes concerned with UV protection. Here, we investigate the interaction of UVR8 with chromatin. Using antibodies specific to UVR8 in chromatin immunoprecipitation (ChiP) assays with wild-type plants, we show that native UVR8 binds to chromatin in vivo. Similar experiments using an anti-GFP antibody with plants expressing a GFP-UVR8 fusion show that UVR8 associates with a relatively small region of chromatin containing the HY5 gene. UVR8 interacts with chromatin containing the promoter regions of other genes, but not with all the genes it regulates. UV-B is not required for the interaction of UVR8 with chromatin because association with several gene loci is observed in the absence of UV-B. Pulldown assays demonstrate that UVR8 associates with histones in vivo and competition experiments indicate that the interaction is preferentially with histone H2B. ChIP experiments using antibodies that recognize specific histone modifications indicate that the UV-B-stimulated transcription of some genes may be correlated with histone modification. In particular, the ELIP1 promoter showed a significant enrichment of diacetyl histone H3 (K9/K14) following UV-B exposure. These findings increase understanding of the interaction of the key UV-B-specific regulator UVR8 with chromatin.

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