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First published online February 18, 2009


Journal of Cell Science 122, 504e (2009)
© The Company of Biologists Limited
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In this issue

Neuronal precursors do the Mash1


Figure 1

The proliferation of cerebellar granular neuronal precursors (CGNPs) during the development of the cerebellum is promoted by several signals, including the transcription factor MYCN, which promotes cell division by activating the cyclin D2 promoter. However, the differentiation of CGNPs into neurons requires cell-cycle exit, which can be triggered by exposure to various anti-mitotic stimuli. Murine Mash1 is a transcription factor that is reportedly involved in this process, but what is the molecular basis for its proneural function? Rubén Álvarez-Rodríguez and Sebastián Pons (p. 595) now show that Mash1 inhibits proliferation by binding to, and thereby repressing, pro-mitotic target genes that are activated by MYCN. Owing to the specificity of both Mash1 and MYCN for regulatory sequences known as E-box motifs, these transcription factors compete for binding of the cyclin D2 promoter, with repression by Mash1 acting dominantly over the inducing activity of MYCN. This work provides new insight into the molecular events that underlie neuronal proliferation and differentiation in mice.


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Related articles in JCS:

Expression of the proneural gene encoding Mash1 suppresses MYCN mitotic activity
Rubén Álvarez-Rodríguez and Sebastián Pons
JCS 2009 122: 595-599. [Abstract] [Full Text]  




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