Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
1994-12-2
pubmed:databankReference
pubmed:abstractText
A recently identified gene encoding a metalloprotease-like, disintegrin-like, cysteine-rich protein (MDC) represents a candidate tumor suppressor gene for human breast cancer based on its location within a minimal region of chromosome 17q21 previously defined by tumor deletion mapping. The work reported here has shown that the MDC gene consists of 28 exons interrupted by relatively short introns, most of them 67 bp to 5 kb in length. We have identified two forms of transcripts generated by alternative splicing. The more abundant form encodes a protein of 769 amino acids; the other, a previously described cDNA, encodes 524 amino acids. Exons 1a, 1b, 1c, 1d, and 2-7 encode a proprotein domain; exons 7-13, a metalloprotease-like domain; exons 14-17, a disintegrin domain; exons 18-22, a cysteine-rich domain, including an epidermal growth factor (EGF)-like repeat domain within exons 21 and 22; exon 23, a transmembrane domain; and exons 24 and 25, a short cytoplasmic domain. These results show that human MDC contains a mosaic of exons capable of encoding several functional domains.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0301-0171
pubmed:author
pubmed:issnType
Print
pubmed:volume
68
pubmed:geneSymbol
MDC
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
39-44
pubmed:dateRevised
2009-9-2
pubmed:meshHeading
pubmed-meshheading:7956356-ADAM Proteins, pubmed-meshheading:7956356-Alternative Splicing, pubmed-meshheading:7956356-Amino Acid Sequence, pubmed-meshheading:7956356-Animals, pubmed-meshheading:7956356-Brain, pubmed-meshheading:7956356-Breast, pubmed-meshheading:7956356-Breast Neoplasms, pubmed-meshheading:7956356-Chromosome Mapping, pubmed-meshheading:7956356-Chromosomes, Human, Pair 17, pubmed-meshheading:7956356-DNA, Complementary, pubmed-meshheading:7956356-Epidermal Growth Factor, pubmed-meshheading:7956356-Exons, pubmed-meshheading:7956356-Female, pubmed-meshheading:7956356-Gene Library, pubmed-meshheading:7956356-Genes, Tumor Suppressor, pubmed-meshheading:7956356-Guinea Pigs, pubmed-meshheading:7956356-Humans, pubmed-meshheading:7956356-Introns, pubmed-meshheading:7956356-Male, pubmed-meshheading:7956356-Molecular Sequence Data, pubmed-meshheading:7956356-Ovary, pubmed-meshheading:7956356-Protein Biosynthesis, pubmed-meshheading:7956356-Proteins, pubmed-meshheading:7956356-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:7956356-Restriction Mapping, pubmed-meshheading:7956356-Sequence Homology, Amino Acid, pubmed-meshheading:7956356-Sequence Homology, Nucleic Acid, pubmed-meshheading:7956356-Testis, pubmed-meshheading:7956356-Tumor Suppressor Proteins
pubmed:year
1995
pubmed:articleTitle
Human metalloprotease/disintegrin-like (MDC) gene: exon-intron organization and alternative splicing.
pubmed:affiliation
Department of Biochemistry, Cancer Institute, Tokyo, Japan.
pubmed:publicationType
Journal Article, Comparative Study