Morphogenesis of Doublefoot (Dbf), a mouse mutant with polydactyly and craniofacial defects

被引:13
|
作者
Hayes, C
Lyon, MF
Morriss-Kay, GM
机构
[1] Univ Oxford, Dept Human Anat, Oxford OX1 3QX, England
[2] MRC, Mammalian Genet Unit, Harwell, Berks, England
关键词
limb development; Sonic hedgehog;
D O I
10.1046/j.1469-7580.1998.19310081.x
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We report the morphogenesis of a new mouse mutant, Doublefoot (Dbf). The major phenotypic features involve the limb and craniofacial regions. There is polydactyly of all 4 limbs, with typically 6-8 digits per limb. All of the digits are triphalangeal; some show bifurcations and some are not attached to the carpus/tarsus. The carpus and tarsus are broader than normal, and their elements are partially fused. There are also tibial defects. Mutant embryos show a diencephalic bulge on d 10.0, with older animals exhibiting broadened and bulbous skulls sometimes with an additional midline skeletal element, shortened snouts and bulging eyes. Homozygotes, which do not survive beyond d 15, show midline facial clefting. In this study of the embryonic and fetal development of Dbf animals, we focus on the morphogenesis of the limbs and head, and discuss the possible molecular developmental mechanisms.
引用
收藏
页码:81 / 91
页数:11
相关论文
共 50 条
  • [41] Expression of Evc2 in craniofacial tissues and craniofacial bone defects in Evc2 knockout mouse
    Badri, Mohammed K.
    Zhang, Honghao
    Ohyama, Yoshio
    Venkitapathi, Sundharamani
    Alamoudi, Ahmed
    Kamiya, Nobuhiro
    Takeda, Haruko
    Ray, Manas
    Scott, Greg
    Tsuji, Takehito
    Kunieda, Tetsuo
    Mishina, Yuji
    Mochida, Yoshiyuki
    ARCHIVES OF ORAL BIOLOGY, 2016, 68 : 142 - 152
  • [42] Defects in tracheoesophageal and lung morphogenesis in Nkx2.1(-/-) mouse embryos
    Minoo, P
    Su, GS
    Drum, H
    Bringas, P
    Kimura, S
    DEVELOPMENTAL BIOLOGY, 1999, 209 (01) : 60 - 71
  • [43] Mouse pigpen encodes a nuclear protein whose expression is developmentally regulated during craniofacial morphogenesis
    Alappat, SR
    Zhang, MF
    Zhao, X
    Alliegro, MA
    Alliegro, MC
    Burdsal, CA
    MOLECULAR BIOLOGY OF THE CELL, 2000, 11 : 55A - 55A
  • [44] Mouse pigpen encodes a nuclear protein whose expression is developmentally regulated during craniofacial morphogenesis
    Alappat, SR
    Zhang, MF
    Zhao, X
    Alliegro, MA
    Alliegro, MC
    Burdsal, CA
    DEVELOPMENTAL DYNAMICS, 2003, 228 (01) : 59 - 71
  • [45] CRANIOFACIAL DEFECTS IN HETEROZYGOTES FOR THE MOUSE MUTATION, 1ST ARCH (FAR)
    HARRIS, MJ
    JURILOFF, DM
    TERATOLOGY, 1987, 35 (02) : A45 - A46
  • [46] A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35
    Hayes, C
    Rump, A
    Cadman, MR
    Harrison, M
    Evans, EP
    Lyon, MF
    Morriss-Kay, GM
    Rosenthal, A
    Brown, SDM
    GENOMICS, 2001, 78 (03) : 197 - 205
  • [47] Mixed-mode pattern in Doublefoot mutant mouse limb -: Turing reaction-diffusion model on a growing domain during limb development
    Miura, Takashi
    Shiota, Kohei
    Morriss-Kay, Gillian
    Maini, Philip K.
    JOURNAL OF THEORETICAL BIOLOGY, 2006, 240 (04) : 562 - 573
  • [48] Embryonic cardiomyocyte hypoplasia and craniofacial defects in Gαq/Gα11-mutant mice
    Offermanns, S
    Zhao, LP
    Gohla, A
    Sarosi, I
    Simon, MI
    Wilkie, TM
    EMBO JOURNAL, 1998, 17 (15): : 4304 - 4312
  • [49] Craniofacial Defects Persist in Eftud2 mutant mice with P53 Deletion
    Beauchamp, Marie-Claude
    Boucher, Alexia
    Dong, Yanchen
    Majewska, Loydie J.
    FASEB JOURNAL, 2022, 36
  • [50] doubleridge, a new mouse mutant with an atypical apical ectodermal ridge (AER) resulting in postaxial polydactyly and syndactyly.
    MacDonald, BT
    Adamska, M
    Meisler, MH
    DEVELOPMENTAL BIOLOGY, 2002, 247 (02) : 516 - 516