Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: Mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches

被引:380
作者
Qiu, MS
Bulfone, A
Ghattas, I
Meneses, JJ
Christensen, L
Sharpe, PT
Presley, R
Pedersen, RA
Rubenstein, JLR
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT PSYCHIAT, CTR NEUROBIOL & PSYCHIAT, NINA IRELAND LAB DEV NEUROBIOL, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, PROGRAM NEUROSCI, SAN FRANCISCO, CA 94143 USA
[3] UNIV CALIF SAN FRANCISCO, PROGRAM DEV BIOL, SAN FRANCISCO, CA 94143 USA
[4] UNIV WALES COLL CARDIFF, ANAT UNIT, CARDIFF CF1 3NS, S GLAM, WALES
[5] UNIV LONDON, GUYS HOSP, DEPT CRANIOFACIAL DEV, LONDON, ENGLAND
[6] UNIV CALIF SAN FRANCISCO, DEPT OBSTET GYNECOL & REPROD SCI, REPROD GENET DIV, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1006/dbio.1997.8556
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Dir homeobox gene family is expressed in a complex pattern within the embryonic craniofacial ectoderm and ectomesenchyme. A previous study established that Dlx-2 is essential for development of proximal regions of the murine first and second branchial arches. Here we describe the craniofacial phenotype of mice with mutations in Dlx-1 and Dlx-1 and -2. The skeletal and soft tissue analyses of mice with Dlx-1 and Dlx-1 and -2 mutations provide additional evidence that the Dir genes regulate proximodistal patterning of the branchial arches. This analysis also elucidates distinct and overlapping roles for Dlx-1 and Dlx-2 in craniofacial development. furthermore, mice lacking both Dlx-1 and -2 have unique abnormalities, including the absence of maxillary molars. Dlx-1 and -2 are expressed in the proximal and distal first and second arches, yet only the proximal regions are abnormal. The nested expression patterns of Dlx-1, -2, -3, -5, and -6 provide evidence for a model that predicts the region-specific requirements for each gene. Finally, the Dlx-2 and Dlx-1 and -2 mutants have ectopic skull components that resemble bones and cartilages found in phylogenetically more primitive vertebrates. (C) 1997 Academic Press.
引用
收藏
页码:165 / 184
页数:20
相关论文
共 74 条
  • [71] Woods C.A., 1985, Evolutionary relationships among rodents, P515
  • [72] YAMADA G, 1995, DEVELOPMENT, V121, P2917
  • [73] RDLX, A NOVEL DISTAL-LESS-LIKE HOMEOPROTEIN IS EXPRESSED IN DEVELOPING CARTILAGES AND DISCRETE NEURONAL TISSUES
    ZHAO, GQ
    ZHAO, SR
    ZHOU, X
    EBERSPAECHER, H
    SOLURSH, M
    DECROMBRUGGHE, B
    [J]. DEVELOPMENTAL BIOLOGY, 1994, 164 (01) : 37 - 51
  • [74] Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene
    Zhao, Q
    Behringer, RR
    deCrombrugghe, B
    [J]. NATURE GENETICS, 1996, 13 (03) : 275 - 283