Constitutive activation of the thyrotropin receptor by mutating CYS-636 in the sixth transmembrane segment

被引:12
作者
Kosugi, S
Mori, T
机构
[1] Department of Laboratory Medicine, Kyoto University, School of Medicine
关键词
D O I
10.1006/bbrc.1996.0809
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
The rat thyrotropin receptor (TSHR) has 7 Cys residues in its transmembrane (TM) segments. We investigated the roles of these Cys residues by individually mutating each to Ser, transfecting the mutant DNA into Cos-7 cells and measuring TSH binding and cAMP/phosphoinositide (PIP2) responses to TSR and Graves' IgGs. Mutation of Cys-636 in the 6th TM helix to Ser markedly increased cAMP level without stimulation. Constitutive activation by this mutation contributes to a more complete map for activating TSHR mutation. Mutation of other Cys residues partially impaired responses but no mutants showed complete loss of receptor function, indicating that these residues have no major contribution to the overall 3-D structure of the TSHR. (C) 1996 Academic Press, Inc.
引用
收藏
页码:713 / 717
页数:5
相关论文
共 15 条
[1]   SPECIFIC ANTIBODY TO THE THYROTROPIN RECEPTOR IDENTIFIES MULTIPLE RECEPTOR FORMS IN MEMBRANES OF CELLS TRANSFECTED WITH WILD-TYPE RECEPTOR COMPLEMENTARY DEOXYRIBONUCLEIC-ACID - CHARACTERIZATION OF THEIR RELEVANCE TO RECEPTOR SYNTHESIS, PROCESSING, STRUCTURE, AND FUNCTION [J].
BAN, T ;
KOSUGI, S ;
KOHN, LD .
ENDOCRINOLOGY, 1992, 131 (02) :815-829
[2]   ROLE OF EXTRACELLULAR DISULFIDE-BONDED CYSTEINES IN THE LIGAND-BINDING FUNCTION OF THE BETA-2-ADRENERGIC RECEPTOR [J].
DOHLMAN, HG ;
CARON, MG ;
DEBLASI, A ;
FRIELLE, T ;
LEFKOWITZ, RJ .
BIOCHEMISTRY, 1990, 29 (09) :2335-2342
[3]  
FRASER CM, 1989, J BIOL CHEM, V264, P9266
[4]  
KJELSBERG MA, 1992, J BIOL CHEM, V267, P1430
[5]   TSH RECEPTOR AND LH RECEPTOR, 1995 [J].
KOSUGI, S ;
MORI, T .
ENDOCRINE JOURNAL, 1995, 42 (05) :587-606
[6]  
KOSUGI S, 1992, J BIOL CHEM, V267, P24153
[7]   SUBSTITUTIONS OF DIFFERENT REGIONS OF THE 3RD CYTOPLASMIC LOOP OF THE THYROTROPIN (TSH) RECEPTOR HAVE SELECTIVE EFFECTS ON CONSTITUTIVE, TSH-RECEPTOR, AND TSH-RECEPTOR AUTOANTIBODY-STIMULATED PHOSPHOINOSITIDE AND 3',5'-CYCLIC ADENOSINE-MONOPHOSPHATE SIGNAL GENERATION [J].
KOSUGI, S ;
OKAJIMA, F ;
BAN, T ;
HIDAKA, A ;
SHENKER, A ;
KOHN, LD .
MOLECULAR ENDOCRINOLOGY, 1993, 7 (08) :1009-1020
[8]   ROLE OF CYSTEINE RESIDUES IN THE EXTRACELLULAR DOMAIN AND EXOPLASMIC LOOPS OF THE TRANSMEMBRANE DOMAIN OF THE TSH RECEPTOR - EFFECT OF MUTATION TO SERINE ON TSH RECEPTOR ACTIVITY AND RESPONSE TO THYROID STIMULATING AUTOANTIBODIES [J].
KOSUGI, S ;
BAN, T ;
AKAMIZU, T ;
KOHN, LD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 189 (03) :1754-1762
[9]   GENETIC-HETEROGENEITY OF CONSTITUTIVELY ACTIVATING MUTATIONS OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY [J].
LAUE, L ;
CHAN, WY ;
HSUEH, AJW ;
KUDO, M ;
HSU, SY ;
WU, SM ;
BLOMBERG, LA ;
CUTLER, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) :1906-1910
[10]   THE UNIQUE EXTRACELLULAR DISULFIDE LOOP OF THE GLYCINE RECEPTOR IS A PRINCIPAL LIGAND-BINDING ELEMENT [J].
RAJENDRA, S ;
VANDENBERG, RJ ;
PIERCE, KD ;
CUNNINGHAM, AM ;
FRENCH, PW ;
BARRY, PH ;
SCHOFIELD, PR .
EMBO JOURNAL, 1995, 14 (13) :2987-2998