2 HUMAN GLUTAMATE DECARBOXYLASES, 65-KDA GAD AND 67-KDA GAD, ARE EACH ENCODED BY A SINGLE GENE

被引:440
作者
BU, DF
ERLANDER, MG
HITZ, BC
TILLAKARATNE, NJK
KAUFMAN, DL
WAGNERMCPHERSON, CB
EVANS, GA
TOBIN, AJ
机构
[1] UNIV CALIF LOS ANGELES,DEPT BIOL,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,INST MOLEC BIOL,LOS ANGELES,CA 90024
[3] UNIV CALIF LOS ANGELES,NEUROSCI PROGRAM,LOS ANGELES,CA 90024
[4] UNIV CALIF LOS ANGELES,DEPT PSYCHIAT & BIOBEHAV SCI,LOS ANGELES,CA 90024
[5] UNIV CALIF LOS ANGELES,BRAIN RES INST,LOS ANGELES,CA 90024
[6] SALK INST,MOLEC GENET LAB,SAN DIEGO,CA 92186
关键词
GAMMA-AMINOBUTYRIC ACID; INSULIN-DEPENDENT DIABETES-MELLITUS; CHROMOSOME-2Q; CHROMOSOME-10P;
D O I
10.1073/pnas.89.6.2115
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report the isolation and sequencing of cDNAs encoding two human glutamate decarboxylases (GADs; L-glutamate 1-carboxy-lyase, EC 4.1.1.15), GAD65 and GAD67. Human GAD65 cDNA encodes a M(r) 65,000 polypeptide, with 585 amino acid residues, whereas human GAD67 encodes a M(r) 67,000 polypeptide, with 594 amino acid residues. Both cDNAs direct the synthesis of enzymatically active GADs in bacterial expression systems. Each cDNA hybridizes to a single species of brain mRNA and to a specific set of restriction fragments in human genomic DNA. In situ hybridization of fluorescently labeled GAD probes to human chromosomes localizes the human GAD65 gene to chromosome 10p11.23 and the human GAD67 gene to chromosome 2q31. We conclude that GAD65 and GAD67 each derive from a single separate gene. The cDNAs we describe should allow the bacterial production of test antigens for the diagnosis and prediction of insulin-dependent diabetes mellitus.
引用
收藏
页码:2115 / 2119
页数:5
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