HUMAN ADENOSINE A(1) RECEPTOR GENE - SYSTEMATIC SCREENING FOR DNA-SEQUENCE VARIATION AND LINKAGE MAPPING ON CHROMOSOME 1Q31-32.1 USING A SILENT POLYMORPHISM IN THE CODING REGION

被引:7
作者
DECKERT, J
NOTHEN, MM
BRYANT, SP
REN, HZ
WOLF, HK
STILES, GL
SPURR, NK
PROPPING, P
机构
[1] IMPERIAL CANC RES FUND,S MIMMS EN6 3LD,HERTS,ENGLAND
[2] DUKE UNIV,MED CTR,DEPT CARDIOL,DURHAM,NC 27710
[3] UNIV BONN,INST NEUROPATHOL,D-53127 BONN,GERMANY
关键词
D O I
10.1006/bbrc.1995.2330
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenosine is a major inhibitory neuromodulator in the central nervous system. One of the receptors mediating the central effects of adenosine is the adenosine A(1) receptor. We performed a systematic mutation scan of the coding region of the adenosine A(1) receptor gene to explore its variability in the general population investigating 40 unrelated healthy subjects by single-strand conformation analysis no sequence changes of likely functional relevance were observed. We detected, however, a frequent T to G substitution at nucleotide position 716 which constitutes the first variant described in an adenosine receptor gene. It was used for fine scale linkage mapping of the A(1) gene. Employing a polymerase-chain-reaction based restriction assay, we genotyped 7 CEPH families (Centre d'Etude du Polymorphisme Humaine) and mapped the receptor in a gene cluster around the renin gene on chromosome lq31-32.1 In addition, we utilized the 716T/G polymorphism to demonstrate biallelic expression of the adenosine A(1) receptor gene in adult human brain. (C) 1995 Academic Press, Inc.
引用
收藏
页码:614 / 621
页数:8
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