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PMID: 9801158 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers.

FEBS letters ·Vol. 436 ·No. 3 ·1998-10-09 ·Pages 403-10

Engelman JA, Zhang XL, Lisanti MP

Abstract

The (CA)n microsatellite repeat marker D7S522 is located on human chromosome 7q31.1 and is frequently deleted in a variety of human cancers, including squamous cell carcinomas of the head and neck, prostate cancers, renal cell carcinomas, ovarian adenocarcinomas, colon carcinomas, and breast cancers. In addition, D7S522 spans FRA7G, a known common fragile site on human chromosome 7. Based on these studies, it has been proposed that an as yet unidentified tumor suppressor gene (or genes) is contained within or located in close proximity to this locus. However, the identity of the candidate tumor suppressor gene at the D7S522 locus remains unknown. Here, we show that the human genes encoding caveolins 1 and 2 are contained within the same human genomic BAC clones and co-localize to the q31.1-q31.2 region of human chromosome 7, as seen by FISH analysis. In addition, we determined the intron-exon boundaries of the human caveolin-1 and -2 genes. The human caveolin-1 gene contains three exons, while the human caveolin-2 gene contains two exons. Interestingly, the boundary of the last exon of the human caveolin-1 and caveolin-2 genes are analogous, suggesting that they arose through gene duplication at this locus. (CA)n microsatellite repeat marker analysis of these caveolin genomic clones indicates they contain the marker D7S522 (located at 7q31.1), but not other microsatellite repeat markers tested. The close proximity of caveolins 1 and 2 to the D7S522 locus was independently confirmed by using a panel of MIT/Whitehead human STS markers that are known to map in the neighborhood of the D7S522 locus. As it has been previously shown that caveolin 1 possesses transformation suppressor activity (Koleske, A.J., Baltimore, D. and M.P. Lisanti (1995) Proc. Natl. Acad. Sci. USA 92, 1381-1385; Engelman, J.A. et al. (1997) J. Biol. Chem. 272, 16374-16381), we propose that the caveolin-1 gene may represent the candidate tumor suppressor gene at the D7S522 locus on human chromosome 7q31.1.

MeSH Terms
Amino Acid Sequence Base Sequence Caveolin 1 Caveolin 2 Caveolins Chromosome Fragile Sites Chromosome Fragility Chromosome Mapping Chromosomes, Human, Pair 7 Cloning, Molecular DNA Primers Exons Female Gene Deletion Genes, Tumor Suppressor Genetic Markers Genomic Library Humans Male Membrane Proteins/chemistry,genetics Molecular Sequence Data Neoplasms/genetics Reverse Transcriptase Polymerase Chain Reaction Sequence Alignment Sequence Homology, Nucleic Acid
Chemicals
CAV1 protein, human Caveolin 1 Caveolin 2 Caveolins DNA Primers Genetic Markers Membrane Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Engelman J A
Department of Molecular Pharmacology and the Albert Einstein Cancer Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Zhang X L
Lisanti M P
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1998-10-09
Pages
403-10
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NIGMS NIH HHS · GM-50443 · United States
NIGMS NIH HHS · T32-GM07288 · United States
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