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
  • [31] Inactivation of Cdc42 in Neural Crest Cells Causes Craniofacial and Cardiovascular Morphogenesis Defects
    Liu, Yang
    Jin, Yixin
    Li, Jieli
    Seto, Edward
    Blazo, Maria
    Zhang, Shenyuan L.
    Peng, Xu
    CIRCULATION, 2013, 128 (22)
  • [32] UCHIDA RAT (RSEY) - A NEW MUTANT RAT WITH CRANIOFACIAL ABNORMALITIES RESEMBLING THOSE OF THE MOUSE SEY MUTANT
    FUJIWARA, M
    UCHIDA, T
    OSUMIYAMASHITA, N
    ETO, K
    DIFFERENTIATION, 1994, 57 (01) : 31 - 38
  • [33] INTERACTION OF THE MUTANT-GENES OF FI, OR AND MI IN THE EYE MOUSE MORPHOGENESIS
    KONYUKHOV, BV
    SAZHINA, MV
    IZVESTIYA AKADEMII NAUK SSSR SERIYA BIOLOGICHESKAYA, 1983, (01): : 100 - 110
  • [34] Neuronal migration defects in the Loa dynein mutant mouse
    Ori-McKenney, Kassandra M.
    Vallee, Richard B.
    NEURAL DEVELOPMENT, 2011, 6
  • [35] Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia
    Tong, Dan
    Colley, Deanne
    Thoo, Renee
    Li, Tony Y.
    Plantes, Isabelle
    Laird, Dale W.
    Bai, Donglin
    Kidder, Gerald M.
    DISEASE MODELS & MECHANISMS, 2009, 2 (3-4) : 157 - 167
  • [36] Neuronal migration defects in the Loa dynein mutant mouse
    Kassandra M Ori-McKenney
    Richard B Vallee
    Neural Development, 6
  • [37] Molecular studies of preaxial polydactyly in three North American families and a novel mouse mutant.
    Hing, AV
    Cook, S
    Dobbs, MB
    Syed, N
    Davisson, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 629 - 629
  • [38] Novel Genes in Bone Biology: Characterisation of the Craniofacial Phenotype of the YODA Mutant Mouse
    Kurar, L.
    Perry, M. J.
    BRITISH JOURNAL OF SURGERY, 2015, 102 : 206 - 206
  • [39] Hyperactivity, Memory Defects, and Craniofacial Abnormalities in Zebrafish fmr1 Mutant Larvae
    Jia Hu
    Lei Chen
    Jian Yin
    Huancai Yin
    Yinong Huang
    Jingjing Tian
    Behavior Genetics, 2020, 50 : 152 - 160
  • [40] Hyperactivity, Memory Defects, and Craniofacial Abnormalities in Zebrafish fmr1 Mutant Larvae
    Hu, Jia
    Chen, Lei
    Yin, Jian
    Yin, Huancai
    Huang, Yinong
    Tian, Jingjing
    BEHAVIOR GENETICS, 2020, 50 (03) : 152 - 160