THE HUMAN PERIPHERAL-TYPE BENZODIAZEPINE RECEPTOR - REGIONAL MAPPING OF THE GENE AND CHARACTERIZATION OF THE RECEPTOR EXPRESSED FROM CDNA

被引:34
作者
CHANG, YJ
MCCABE, RT
RENNERT, H
BUDARF, ML
SAYEGH, R
EMANUEL, BS
SKOLNICK, P
STRAUSS, JF
机构
[1] UNIV PENN,SCH MED,DEPT OBSTET & GYNECOL,771 CLIN RES BLDG,422 CURIE BLVD,PHILADELPHIA,PA 19104
[2] NIDDK,NEUROSCI LAB,BETHESDA,MD 20892
[3] CHILDRENS HOSP PHILADELPHIA,DIV HUMAN GENET & MOLEC BIOL,PHILADELPHIA,PA 19104
关键词
D O I
10.1089/dna.1992.11.471
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
A cDNA for the human "peripheral-type" benzodiazepine receptor (PBR) was isolated from a liver cDNA library. The 851-nucleotide probe hybridized with a approximately 1 kb mRNA in Northern blots of RNA extracted from various human tissues and cell lines. The human PBR probe was hybridized to DNA from a somatic cell hybrid mapping panel to determine that the gene maps to chromosome 22. With a regional mapping panel for chromosome 22, we localized the gene within band 22q13.31. The ligand-binding properties of the receptor expressed from the cDNA were examined in transient expression experiments and compared to the endogenous human PBR. The PBR ligand [H-3]PK 11195 had high affinity for the expressed receptor in COS-1 cells, but the affinities of a pair of isoquinoline propanamide enantiomers differed remarkably in expressed and endogenous human PBR. These findings reveal that the host cell and/or post-translational modification may have an important influence on PBR function.
引用
收藏
页码:471 / 480
页数:10
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