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Review
Nature Neuroscience  5, 1265 - 1269 (2002)
doi:10.1038/nn1202-1265

Asymmetric segregation of Numb: a mechanism for neural specification from Drosophila to mammals

Michel Cayouette1, 2 & Martin Raff1

1  MRC Laboratory for Molecular Cell Biology and Cell Biology Unit, University College London, Gower Street, London WC1E 6BT, UK

2  Present address: Stanford University, Department of Neurobiology, Fairchild Building, 299 Campus Drive, D231, Stanford, California 94305-5125, USA

Correspondence should be addressed to Michel Cayouette m.cayouette@stanford.edu
It is a major challenge to understand how the neuroepithelial cells of the developing CNS choose between alternative cell fates to generate cell diversity. In invertebrates such as Drosophila melanogaster and Caenorhabditis elegans, asymmetric segregation of cell-fate determining proteins or mRNAs to the two daughter cells during precursor cell division plays a crucial part in cell diversification. There is increasing evidence that this mechanism also operates in vertebrate neural development and that Numb proteins, which function as cell-fate determinants during Drosophila development, may also function in this way in vertebrates. Recent studies on mouse cortical progenitor cells have provided the strongest evidence yet that this is the case. Here, we review these and other findings that suggest an important role for the asymmetric segregation of Numb proteins in vertebrate neural development.

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REFERENCE
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Nature Neuroscience
ISSN: 1097-6256
EISSN: 1546-1726
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