Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse

被引:217
作者
Ware, ML
Fox, JW
Gonzalez, JL
Davis, NM
deRouvroit, CL
Russo, CJ
Chua, SC
Goffinet, AM
Walsh, CA
机构
[1] HARVARD UNIV, SCH MED,BETH ISRAEL MED CTR,DIV NEUROGENET, HARVARD INST MED,DEPT NEUROL, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, PROGRAM NEUROSCI, BOSTON, MA 02115 USA
[3] HARVARD UNIV, SCH MED, PROGRAM BIOL & BIOMED SCI, BOSTON, MA 02115 USA
[4] FAC UNIV NOTRE DAME PAIX, SCH MED, DEPT PHYSIOL, B-5000 NAMUR, BELGIUM
[5] ROCKEFELLER UNIV, HUMAN BEHAV & METAB LAB, NEW YORK, NY 10021 USA
关键词
D O I
10.1016/S0896-6273(00)80936-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although accurate long-distance neuronal migration is a cardinal feature of cerebral cortical development, little is known about control of this migration. The scrambler(scm) mouse shows abnormal cortical lamination that is indistinguishable from reeler. Genetic and physical mapping of scm identified yeast artificial chromosomes containing an exon of mdab1, a homolog of Drosophila disabled, which encodes a phosphoprotein that binds nonreceptor tyrosine kinases. mdab1 transcripts showed abnormal splicing in scm homozygotes, with 1.5 kb of intracisternal A particle retrotransposon sequence inserted into the mdab1 coding region in antisense orientation, producing a mutated and truncated predicted protein. Therefore, mdab1 is most likely the scm gene, thus implicating nonreceptor tyrosine kinases in neuronal migration and lamination in developing cerebral cortex.
引用
收藏
页码:239 / 249
页数:11
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  • [1] Sequence, genomic structure, and chromosomal assignment of human DOC-2
    Albertsen, HM
    Smith, SA
    Melis, R
    Williams, B
    Holik, P
    Stevens, J
    White, R
    [J]. GENOMICS, 1996, 33 (02) : 207 - 213
  • [2] INSERTIONAL MUTAGENESIS BY TRANSPOSABLE ELEMENTS IN THE MAMMALIAN GENOME
    AMARIGLIO, N
    RECHAVI, G
    [J]. ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1993, 21 (03) : 212 - 218
  • [3] Ausubel FM., 1994, Curr. Protoc. Mol. Biol
  • [4] A YAC CONTIG CONTAINING THE REELER LOCUS WITH PRELIMINARY CHARACTERIZATION OF CANDIDATE GENE FRAGMENTS
    BAR, I
    DEROUVROIT, CL
    ROYAUX, I
    KRIZMAN, DB
    DERNONCOURT, C
    RUELLE, D
    BECKERS, MC
    GOFFINET, AM
    [J]. GENOMICS, 1995, 26 (03) : 543 - 549
  • [5] A HIGH-RESOLUTION GENETIC-MAP OF MOUSE CHROMOSOME-5 ENCOMPASSING THE REELER (RL) LOCUS
    BECKERS, MC
    BAR, I
    HUYNHTHU, T
    DERNONCOURT, C
    BRUNIALTI, AL
    MONTAGUTELLI, X
    GUENET, JL
    GOFFINET, AM
    [J]. GENOMICS, 1994, 23 (03) : 685 - 690
  • [6] NCAM-DEPENDENT NEURITE OUTGROWTH IS INHIBITED IN NEURONS FROM FYN-MINUS MICE
    BEGGS, HE
    SORIANO, P
    MANESS, PF
    [J]. JOURNAL OF CELL BIOLOGY, 1994, 127 (03) : 825 - 833
  • [7] NCAM140 interacts with the focal adhesion kinase p125(fak) and the SRC-related tyrosine kinase p59(fyn)
    Beggs, HE
    Baragona, SC
    Hemperly, JJ
    Maness, PF
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) : 8310 - 8319
  • [8] NEOCORTICAL HISTOGENESIS IN NORMAL AND REELER MICE - A DEVELOPMENTAL-STUDY BASED UPON [H-3] THYMIDINE AUTORADIOGRAPHY
    CAVINESS, VS
    [J]. DEVELOPMENTAL BRAIN RESEARCH, 1982, 4 (03): : 293 - 302
  • [9] Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality
    Chae, T
    Kwon, YT
    Bronson, R
    Dikkes, P
    Li, E
    Tsai, LH
    [J]. NEURON, 1997, 18 (01) : 29 - 42
  • [10] Phenotypes of mouse diabetes and rat fatty due to mutations in the OB (leptin) receptor
    Chua, SC
    Chung, WK
    WuPeng, XS
    Zhang, YY
    Liu, SM
    Tartaglia, L
    Leibel, RL
    [J]. SCIENCE, 1996, 271 (5251) : 994 - 996