PREMATURE SUTURE CLOSURE AND ECTOPIC CRANIAL BONE IN MICE EXPRESSING MSX2 TRANSGENES IN THE DEVELOPING SKULL

被引:196
作者
LIU, YH
KUNDU, R
WU, LY
LUO, W
IGNELZI, MA
SNEAD, MI
MAXSON, RE
机构
[1] KENNETH R NORRIS CANC HOSP & INST,DEPT BIOCHEM & MOLEC BIOL,LOS ANGELES,CA 90033
[2] UNIV SO CALIF,SCH DENT,CTR CRANIOFACIAL MOLEC BIOL,LOS ANGELES,CA 90033
关键词
CRANIOSYNOSTOSIS; SKULL DEVELOPMENT; HOMEOBOX; TRANSGENIC MICE;
D O I
10.1073/pnas.92.13.6137
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
The coordinate growth of the brain and skull is achieved through a series of interactions between the developing brain, the growing bones of the skull, and the fibrous joints, or sutures, that unite the bones, These interactions couple the expansion of the brain to the growth of the bony plates at the sutures, Craniosynostosis, the premature fusion of the bones of the skull, is a common birth defect (1 in 3000 live births) that disrupts coordinate growth and often results in profoundly abnormal skull shape. Individuals affected with Boston-type craniosynostosis, an autosomal dominant disorder, bear a mutated copy of MSX2, a homeobox gene thought to function in tissue interactions. Here we show that expression of the mouse counterpart of this mutant gene in the developing skulls of transgenic mice causes craniosynostosis and ectopic cranial bone, These mice provide a transgenic model of craniosynostosis as well as a point of entry into the molecular mechanisms that coordinate the growth of the brain and skull.
引用
收藏
页码:6137 / 6141
页数:5
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