GENOMIC AND CDNA SEQUENCE-ANALYSIS OF THE CELL-MATRIX ADHESION REGULATOR GENE

Citation
H. Durbin et al., GENOMIC AND CDNA SEQUENCE-ANALYSIS OF THE CELL-MATRIX ADHESION REGULATOR GENE, Proceedings of the National Academy of Sciences of the United Statesof America, 94(26), 1997, pp. 14578-14583
Citations number
30
ISSN journal
00278424
Volume
94
Issue
26
Year of publication
1997
Pages
14578 - 14583
Database
ISI
SICI code
0027-8424(1997)94:26<14578:GACSOT>2.0.ZU;2-9
Abstract
The cell matrix adhesion regulator (CMAR) gene has been suggested to b e a signal transduction molecule influencing cell adhesion to collagen and, through this, possibly involved in tumor suppression, The origin ally reported CMAR cDNA was 464 bp long with a tyrosine phosphorylatio n site at the extreme 3' end, which mutagenesis studies had shown to b e central to the function of this gene. Since the discovery of a 4-bp insertion polymorphism within the originally reported coding region, f urther sequence information has been obtained, The cDNA has been exten ded 5' by approximate to 2 kb revealing a 559-bp region showing strong homology to the proposed 5' untranslated sequence of a murine protein kinase receptor family member, variant in kinase (vik), CMAR genomic sequencing has shown the presence of an intron, the intron/exon bounda ry lying within this region of homology. An RNA transcript for CMAR of approximate to 2.5 kb has also been identified, The data suggest comp lex mechanisms for control of expression of two closely associated gen es, CMAR and the vik-associated sequence.