The tumor suppressor Pml regulates cell fate in the developing neocortex.

Abstract:

:The control of cell fate in neural progenitor cells is critical for nervous system development. Nevertheless, the processes involved are only partially known. We found that the expression of the tumor suppressor Pml was restricted to neural progenitor cells (NPCs) in the developing neocortex of the mouse. Notably, in Pml(-/-) cortices, the overall number of proliferating NPCs was increased and transition between the two major progenitor types, radial glial cells and basal progenitors, was impaired. This in turn resulted in reduced differentiation and an overall decrease in the thickness of the cortex wall. In NPCs, Pml regulated the subcellular distribution of the retinoblastoma protein (pRb) and the protein phosphatase 1alpha, triggering pRb dephosphorylation. Together, these findings reveal an unexpected role of Pml in controlling the function of NPCs in the CNS.

journal_name

Nat Neurosci

journal_title

Nature neuroscience

authors

Regad T,Bellodi C,Nicotera P,Salomoni P

doi

10.1038/nn.2251

subject

Has Abstract

pub_date

2009-02-01 00:00:00

pages

132-40

issue

2

eissn

1097-6256

issn

1546-1726

pii

nn.2251

journal_volume

12

pub_type

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