A CONSTITUTIVELY ACTIVE MUTANT PTH-PTHRP RECEPTOR IN JANSEN-TYPE METAPHYSEAL CHONDRODYSPLASIA

被引:499
作者
SCHIPANI, E
KRUSE, K
JUPPNER, H
机构
[1] MASSACHUSETTS GEN HOSP, DEPT MED, ENDOCRINE UNIT, BOSTON, MA 02114 USA
[2] MASSACHUSETTS GEN HOSP, CHILDRENS SERV, BOSTON, MA 02114 USA
[3] HARVARD UNIV, SCH MED, BOSTON, MA 02114 USA
[4] UNIV LUBECK, PADIATRIE KLIN, D-23538 LUBECK, GERMANY
关键词
D O I
10.1126/science.7701349
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
A single heterozygous nucleotide exchange in exon M2 of the gene encoding the parathyroid hormone-parathyroid hormone-related peptide (PTH-PTHrP) receptor was identified in a patient with Jansen-type metaphyseal chondrodysplasia, which changes a strictly conserved histidine residue at position 223 in the receptor's first intracellular loop to arginine. Constitutive, ligand-independent adenosine 3',5'-monophosphate accumulation was observed in COS-7 cells expressing the mutant PTH-PTHrP receptor but not in cells expressing the wild-type receptor. This finding explains the severe ligand-independent hypercalcemia and hypophosphatemia, and most likely the abnormal formation of endochondral bone, in this rare form of short-limbed dwarfism.
引用
收藏
页码:98 / 100
页数:3
相关论文
共 27 条
[1]   PARATHYROID HORMONE-RELATED PEPTIDE-DEPLETED MICE SHOW ABNORMAL EPIPHYSEAL CARTILAGE DEVELOPMENT ALTERED ENDOCHONDRAL BONE-FORMATION [J].
AMIZUKA, N ;
WARSHAWSKY, H ;
HENDERSON, JE ;
GOLTZMAN, D ;
KARAPLIS, AC .
JOURNAL OF CELL BIOLOGY, 1994, 126 (06) :1611-1623
[2]   CLONED, STABLY EXPRESSED PARATHYROID-HORMONE (PTH)/PTH-RELATED PEPTIDE RECEPTORS ACTIVATE MULTIPLE MESSENGER SIGNALS AND BIOLOGICAL RESPONSES IN LLC-PK1 KIDNEY-CELLS [J].
BRINGHURST, FR ;
JUPPNER, H ;
GUO, J ;
URENA, P ;
POTTS, JT ;
KRONENBERG, HM ;
ABOUSAMRA, AB ;
SEGRE, GV .
ENDOCRINOLOGY, 1993, 132 (05) :2090-2098
[3]  
Broadus Arthur E., 1994, P259
[4]  
de Haas W H, 1969, J Bone Joint Surg Br, V51, P290
[5]   HETEROZYGOUS MISSENSE MUTATION IN THE RHODOPSIN GENE AS A CAUSE OF CONGENITAL STATIONARY NIGHT BLINDNESS [J].
DRYJA, TP ;
BERSON, EL ;
RAO, VR ;
OPRIAN, DD .
NATURE GENETICS, 1993, 4 (03) :280-283
[6]   GERMLINE MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE NON-AUTOIMMUNE AUTOSOMAL-DOMINANT HYPERTHYROIDISM [J].
DUPREZ, L ;
PARMA, J ;
VANSANDE, J ;
ALLGEIER, A ;
LECLERE, J ;
SCHVARTZ, C ;
DELISLE, MJ ;
DECOULX, M ;
ORGIAZZI, J ;
DUMONT, J ;
VASSART, G .
NATURE GENETICS, 1994, 7 (03) :396-401
[7]  
Frame B, 1980, PEDIAT DIS RELATED C, P269
[8]   METAPHYSEAL CHONDRODYSPLASIA OF JANSEN [J].
GRAM, PB ;
FLEMING, JL ;
FRAME, B ;
FINE, G .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1959, 41 (05) :951-959
[9]  
HOLT JF, 1969, CLIN DELINEATION BIR, V5, P73
[10]  
Jansen M, 1934, Z ORTHOP CHIR, V61, P253