OSTEOCALCIN CLUSTER - IMPLICATIONS FOR FUNCTIONAL-STUDIES

被引:54
作者
DESBOIS, C [1 ]
KARSENTY, G [1 ]
机构
[1] UNIV TEXAS, MD ANDERSON CANC CTR, DEPT MOLEC GENET, HOUSTON, TX 77030 USA
关键词
BONE EXTRACELLULAR MATRIX; CELL PROLIFERATION; CELL DIFFERENTIATION; OSTEOBLAST; ODONTOBLAST; OSTEOCALCIN; GLA PROTEIN;
D O I
10.1002/jcb.240570302
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
Osteocalcin is a skeletal member of the family of extracellular mineral binding Gla protein. Osteocalcin is synthesized only by the osteoblast and it is secreted into the bone matrix at the time of bone mineralization. The mineral binding properties of osteocalcin as well as its spatial and temporal pattern of expression suggest that it plays a role during bone mineralization, however until now its biological function is unclear. To understand osteocalcin function during skeletogenesis we mutated the two osteocalcin genes by homologous recombination in embryonic stem (ES) cells. Eight targeted clones were identified by Southern analysis using external probes. One of these clones contributed to the germ line of mouse chimera. Interbreeding of heterozygotes is currently in progress. Mutant mice will be useful to understand osteocalcin function in vivo. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:379 / 383
页数:5
相关论文
共 18 条
[1]   THE NEW MOUSE GENETICS - ALTERING THE GENOME BY GENE TARGETING [J].
CAPECCHI, MR .
TRENDS IN GENETICS, 1989, 5 (03) :70-76
[2]   FAMILIAL PROTEIN S DEFICIENCY IS ASSOCIATED WITH RECURRENT THROMBOSIS [J].
COMP, PC ;
NIXON, RR ;
COOPER, MR ;
ESMON, CT .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (06) :2082-2088
[3]  
DESBOIS C, 1994, J BIOL CHEM, V269, P1183
[4]   MOLECULAR-BASIS OF HEMOPHILIA-B - A DEFECTIVE ENZYME DUE TO AN UNPROCESSED PROPEPTIDE IS CAUSED BY A POINT MUTATION IN THE FACTOR-IX PRECURSOR [J].
DIUGUID, DL ;
RABIET, MJ ;
FURIE, BC ;
LIEBMAN, HA ;
FURIE, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :5803-5807
[5]  
FETEIH R, 1990, J BONE MINER RES, V5, P885
[6]   THE MOLECULAR-BASIS OF BLOOD-COAGULATION [J].
FURIE, B ;
FURIE, BC .
CELL, 1988, 53 (04) :505-518
[7]   OSTEOCALCIN AND MATRIX GLA PROTEIN - VITAMIN K-DEPENDENT PROTEINS IN BONE [J].
HAUSCHKA, PV ;
LIAN, JB ;
COLE, DEC ;
GUNDBERG, CM .
PHYSIOLOGICAL REVIEWS, 1989, 69 (03) :990-1047
[8]   STRUCTURE OF THE RAT OSTEOCALCIN GENE AND REGULATION OF VITAMIN-D-DEPENDENT EXPRESSION [J].
LIAN, J ;
STEWART, C ;
PUCHACZ, E ;
MACKOWIAK, S ;
SHALHOUB, V ;
COLLART, D ;
ZAMBETTI, G ;
STEIN, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (04) :1143-1147
[9]   RESORPTION OF IMPLANTED BONE PREPARED FROM NORMAL AND WARFARIN-TREATED RATS [J].
LIAN, JB ;
TASSINARI, M ;
GLOWACKI, J .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (04) :1223-1226
[10]  
PAULI RM, 1987, AM J HUM GENET, V41, P566