Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
1999-9-23
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120978, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120979, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120980, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120981, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120982, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120983, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120984, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120985, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120986, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120987, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120988, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120989, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120990, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120991, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120992, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120993, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120994, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120995, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120996, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120997, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120998, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF120999, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AH008225
pubmed:abstractText
DNA methylation is essential for murine development and is implicated in the control of gene expression. MeCP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of mammalian, nuclear proteins related by the presence in each of an amino acid motif called the methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MeCP2, MBD1 and MBD2 can also repress transcription. We describe the genomic structure and chromosomal localization of the human and murine Mbd1, Mbd2, Mbd3, and Mbd4 genes. We find that the highly similar MBD2 and MBD3 proteins are encoded by genes that map to different chromosomes in humans and mice but show a similar genomic structure. The Mbd1 and Mbd2 genes, in contrast, map together to murine and human Chromosomes (Chrs)18. The Mbd3 and Mbd4 genes map to murine Chrs 10 and 6, respectively, while the human MBD3 and MBD4 genes map to Chrs 19 and 3, respectively.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0938-8990
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
906-12
pubmed:dateRevised
2009-9-29
pubmed:meshHeading
pubmed-meshheading:10441743-Animals, pubmed-meshheading:10441743-Chromosome Mapping, pubmed-meshheading:10441743-Chromosomes, Human, Pair 18, pubmed-meshheading:10441743-Chromosomes, Human, Pair 19, pubmed-meshheading:10441743-Chromosomes, Human, Pair 3, pubmed-meshheading:10441743-DNA, pubmed-meshheading:10441743-DNA Methylation, pubmed-meshheading:10441743-DNA Primers, pubmed-meshheading:10441743-DNA-Binding Proteins, pubmed-meshheading:10441743-Endodeoxyribonucleases, pubmed-meshheading:10441743-Exons, pubmed-meshheading:10441743-Genome, pubmed-meshheading:10441743-Humans, pubmed-meshheading:10441743-In Situ Hybridization, Fluorescence, pubmed-meshheading:10441743-Introns, pubmed-meshheading:10441743-Mice, pubmed-meshheading:10441743-Species Specificity, pubmed-meshheading:10441743-Transcription Factors
pubmed:year
1999
pubmed:articleTitle
Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes.
pubmed:affiliation
Institute of Cell and Molecular Biology, University of Edinburgh, Darwin Building, King's Buildings, Edinburgh EH9 3JR Scotland, UK.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't