GERMLINE MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE NON-AUTOIMMUNE AUTOSOMAL-DOMINANT HYPERTHYROIDISM

被引:316
作者
DUPREZ, L
PARMA, J
VANSANDE, J
ALLGEIER, A
LECLERE, J
SCHVARTZ, C
DELISLE, MJ
DECOULX, M
ORGIAZZI, J
DUMONT, J
VASSART, G
机构
[1] FREE UNIV BRUSSELS,FAC MED,INST RECH INTERDISCIPLINAIRE,BRUSSELS,BELGIUM
[2] CHU NANCY,SERV ENDOCRINOL,NANCY,FRANCE
[3] INST JEAN GODINOT,UNITE MED NUCL & BIOPHYS,REIMS,FRANCE
[4] CTR HOSP REG & UNIV LILLE,SERV CLIN MED,F-59037 LILLE,FRANCE
[5] CTR HOSP LYON SUD,HOSPICES CIVILS LYON,SERV MED INTERNE,PIERRE BENITE,FRANCE
[6] FREE UNIV BRUSSELS,SERV GENET MED,B-1070 BRUSSELS,BELGIUM
关键词
D O I
10.1038/ng0794-396
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The thyrotropin receptor (TSHR), a member of the large family of G protein-coupled receptors, controls both the function and growth of thyroid cells via stimulation of adenylyl cyclase. We report two different mutations in the TSHR gene of affected members of two large pedigrees with non-autoimmune autosomal dominant hyperthyroidism (toxic thyroid hyperplasia), that involve residues in the third (Val509Ala) and seventh (Cys672Tyr) transmembrane segments. When expressed by transfection in COS-7 cells, the mutated receptors display a higher constitutive activation of adenylyl cyclase than wild type. This new disease entity is the germline counterpart of hyperfunctioning thyroid adenomas, in which different somatic mutations with similar functional characteristics have been demonstrated.
引用
收藏
页码:396 / 401
页数:6
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