CHROMOSOMAL ASSIGNMENT OF HUMAN AND RAT HYPERTENSION CANDIDATE GENES - TYPE-1 ANGIOTENSIN-II RECEPTOR GENES AND THE S(A) GENE

Citation
C. Szpirer et al., CHROMOSOMAL ASSIGNMENT OF HUMAN AND RAT HYPERTENSION CANDIDATE GENES - TYPE-1 ANGIOTENSIN-II RECEPTOR GENES AND THE S(A) GENE, Journal of hypertension, 11(9), 1993, pp. 919-925
Citations number
45
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
02636352
Volume
11
Issue
9
Year of publication
1993
Pages
919 - 925
Database
ISI
SICI code
0263-6352(1993)11:9<919:CAOHAR>2.0.ZU;2-E
Abstract
Objective: The chromosomal location of candidate genes for a disease, especially if the disease is multifactorial, is an important datum. Th e objective of the present study was to determine the chromosomal loca tion of candidate hypertensinogenic genes, both in humans and in the r at, a species widely used for animal models of human hypertension. The type 1 angiotensin II receptor (AT1) genes are obvious hypertension c andidate genes, whereas the S(A) gene has recently been shown to coseg regate with hypertension in the rat. Design: The chromosomal location of the relevant genes was determined using somatic cell hybrids segreg ating either human chromosomes or rat chromosomes. The presence of the human or rat genes was determined by the Southern blot method, using rat probes. Results: A single AT1 gene (AT1) was detected in the human genome, and was assigned to chromosome 3, whereas two non-syntenic ge nes were detected in the rat genome, corresponding to the previously i dentified A and B subtypes. They were assigned to the rat chromosome 1 7 (At1a) and 2 (AT1b). The Sa gene was assigned to human chromosome 16 and rat chromosome 1, disclosing a new synteny group retained on rat chromosome 1 and human chromosome 16. Conclusions: These chromosomal a ssignments should be useful for linkage analyses of genes controlling blood pressure. The genes that we studied, and the chromosomes that we identified, deserve special attention in such linkage analyses.