Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects

被引:8
|
作者
Franke, B
Klootwijk, R
Hekking, JWM
de Boer, RT
ten Donkelaar, HJ
Mariman, ECM
van Straaten, HWM
机构
[1] Univ Med Ctr Nijmegen, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[2] Univ Maastricht, Dept Anat & Embryol, Maastricht, Netherlands
[3] Univ Med Ctr Nijmegen, Dept Neurol, Nijmegen, Netherlands
[4] Univ Maastricht, Dept Human Biol, Maastricht, Netherlands
来源
ANATOMY AND EMBRYOLOGY | 2003年 / 207卷 / 03期
关键词
animal model; mes-rhombencephalic exencephaly; tight amnion; axial kinking; embryonic turning;
D O I
10.1007/s00429-003-0345-2
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
Neural tube defects, mostly believed to result from closure defects of the neural tube during embryonic development, are frequently observed congenital malformations in humans. Since the etiology of these defects is not well understood yet, many animal models for neural tube defects, either arising from spontaneous mutations or generated by gene targeting, are being studied. The Bent tail mouse is a model for X-linked neural tube defects. This mutant has a characteristic short and kinked tail. Exencephaly occurs in Bent tail embryos with a frequency of 11-16%. Laterality defects also belong to the phenotypic spectrum. In this study, we analyzed the embryonic phenotype in further detail using scanning electron microscopy during the stages of neurulation. We observed a number of defects in both wild type and Bent tail embryos, including a kinked neural tube, tight amnion, delay in axial rotation and even malrotation. The severity or frequency of most defects, the delay in axial rotation excluded, was significantly higher in Bent tail embryos compared to wild type embryos. Other abnormalities were seen in Bent tail embryos only. These defects were related to anterior and posterior neural tube closure and resulted in exencephaly and a closure delay of the posterior neuropore, respectively. The exencephalic phenotype was further analyzed by light microscopy in ED14 embryos, showing disorganization and overgrowth in the mesencephalon and rhombencephalon. In conclusion, the anterior and posterior neural tube closure defects in the Bent tail are strictly linked to the genetic defect in this mouse. Other phenotypic features described in this study also occur in the wild type genetic background of the Bent tail strain. Apparently, the genetic background contains elements conducive to these developmental abnormalities.
引用
收藏
页码:255 / 262
页数:8
相关论文
共 50 条
  • [31] EFFECT OF HYDROXYUREA ON NEURAL-TUBE DEFECTS IN THE CURLY-TAIL MOUSE
    SELLER, MJ
    PERKINS, KJ
    JOURNAL OF CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY, 1983, 3 (01): : 11 - 17
  • [32] Mouse as a model for multifactorial inheritance of neural tube defects
    Zohn, Irene E.
    BIRTH DEFECTS RESEARCH PART C-EMBRYO TODAY-REVIEWS, 2012, 96 (02) : 193 - 205
  • [33] AN EXPERIMENTAL MOUSE MODEL OF NEURAL-TUBE DEFECTS
    SELLER, MJ
    TERATOLOGY, 1982, 26 (03) : A4 - A4
  • [34] INTERACTION BETWEEN SPLOTCH (SP) AND CURLY TAIL (CT) MOUSE MUTANTS IN THE EMBRYONIC-DEVELOPMENT OF NEURAL-TUBE DEFECTS
    ESTIBEIRO, JP
    BROOK, FA
    COPP, AJ
    DEVELOPMENT, 1993, 119 (01): : 113 - 121
  • [35] Genotype-phenotype analysis in patients with X-linked lissencephaly with abnormal genitalia (XLAG), X-linked infantile spasms and X-linked mental retardation.
    Kato, M
    Peng, Y
    Kretzschmar, E
    Chen, P
    Raca, G
    Kitamura, K
    Sugiyama, N
    Fukuda, T
    Morohashi, K
    Das, S
    Dobyns, WB
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 179 - 179
  • [36] A genetic risk factor for mouse neural tube defects: defining the embryonic basis
    Fleming, A
    Copp, AJ
    HUMAN MOLECULAR GENETICS, 2000, 9 (04) : 575 - 581
  • [37] X-LINKED TSPYL2DEFICIT MOUSE IS ASSOCIATED WITH A PHENOTYPE OF SCHIZOPHRENIA
    Li, Q.
    Wong, Kwun K.
    Wei, Ran
    Lam, Sylvia
    Zhang, Xiao F.
    Sham, Pak C.
    Chua, Siew E.
    Chan, Siu Y.
    McAlonan, Grainne M.
    SCHIZOPHRENIA RESEARCH, 2012, 136 : S191 - S191
  • [38] X-linked loci of Drosophila melanogaster causing defects in the morphology of the embryonic salivary glands
    U. Lammel
    H. Saumweber
    Development Genes and Evolution, 2000, 210 : 525 - 535
  • [39] X-linked loci of Drosophila melanogaster causing defects in the morphology of the embryonic salivary glands
    Lammel, U
    Saumweber, H
    DEVELOPMENT GENES AND EVOLUTION, 2000, 210 (11) : 525 - 535
  • [40] Genotype-phenotype analysis in patients with X-linked lissencephaly with abnormal genitalia (XLAG) and X-linked infantile spasms
    Kato, M
    Peng, Y
    Kitamura, K
    Morohashi, K
    Das, S
    Dobyns, WB
    ANNALS OF NEUROLOGY, 2002, 52 (03) : S116 - S116