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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
23
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pubmed:dateCreated |
2000-1-31
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pubmed:abstractText |
CpG methylation in vertebrates is important for gene silencing, alterations in chromatin structure and genomic stability, and differences in the DNA-methylation status are correlated with imprinting phenomena, carcinogenesis and embryonic development. Methylation signals are interpreted by protein factors that contain shared methyl-CpG-binding domains (MBDs). We have determined the solution structure of the MBD of the human methylation-dependent transcriptional repressor MBD1 by multi-dimensional heteronuclear NMR spectroscopy. It folds into an alpha/beta-sandwich structure with characteristic loops. Basic residues conserved in the MBD family are largely confined to one face of this fold and a flexible loop, which together form a large positively charged surface. Site-directed mutagenesis and chemical shift changes upon complexing with a methylated DNA facilitated identification of this surface as the DNA interaction site. In addition to three basic residues, conserved Tyr34 and Asp32 were shown to be important for the DNA binding.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chromosomal Proteins, Non-Histone,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Transferase,
http://linkedlifedata.com/resource/pubmed/chemical/MBD1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/MECP2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Methyl-CpG-Binding Protein 2,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0261-4189
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6653-61
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pubmed:dateRevised |
2008-11-20
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pubmed:meshHeading |
pubmed-meshheading:10581239-Amino Acid Sequence,
pubmed-meshheading:10581239-Binding Sites,
pubmed-meshheading:10581239-Chromosomal Proteins, Non-Histone,
pubmed-meshheading:10581239-DNA Methylation,
pubmed-meshheading:10581239-DNA-Binding Proteins,
pubmed-meshheading:10581239-Escherichia coli,
pubmed-meshheading:10581239-Glutathione Transferase,
pubmed-meshheading:10581239-Humans,
pubmed-meshheading:10581239-Magnetic Resonance Spectroscopy,
pubmed-meshheading:10581239-Methyl-CpG-Binding Protein 2,
pubmed-meshheading:10581239-Models, Molecular,
pubmed-meshheading:10581239-Molecular Sequence Data,
pubmed-meshheading:10581239-Mutagenesis, Site-Directed,
pubmed-meshheading:10581239-Protein Binding,
pubmed-meshheading:10581239-Recombinant Fusion Proteins,
pubmed-meshheading:10581239-Repressor Proteins,
pubmed-meshheading:10581239-Sequence Homology, Amino Acid,
pubmed-meshheading:10581239-Transcription Factors
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pubmed:year |
1999
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pubmed:articleTitle |
Solution structure of the methyl-CpG-binding domain of the methylation-dependent transcriptional repressor MBD1.
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pubmed:affiliation |
Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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