Reeler:: new tales on an old mutant mouse

被引:0
作者
D'Arcangelo, G [1 ]
Curran, T [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
关键词
D O I
10.1002/(SICI)1521-1878(199803)20:3<235::AID-BIES7>3.3.CO;2-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurological mouse mutants provide an opportunity to dissect the complex mechanisms that underlie vertebrate brain development. Advances in genetic technologies have permitted the identification of genes disrupted in many mutants, allowing a molecular interpretation of the phenotypes, For several decades, the spontaneous mutant mouse reeler has been used as a model for the analysis of the development of laminated brain structures, In this ataxic mutant, the migration of many neurons is aberrant, resulting in disrupted cellular organization, Recently, reelin, the gene disrupted in the reeler mouse, has been identified. reelin encodes a novel extracellular molecule that controls neural cell positioning through mechanisms that are not yet completely understood, Analysis of the expression pattern and the properties of the reelin gene product (Reelin) suggests models for its function during brain development. Furthermore, the recent identification of genes that may function in the Reelin signaling pathway advances our knowledge of the molecular basis of neuronal migration. BioEssays 20: 235-244, 1998. (C) 1998 John Wiley & Sons, Inc.
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页码:235 / 244
页数:10
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