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
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.