CyclinD2 at the edge: splitting up cell fate

Research output: Contribution to journalResearch articleContributedpeer-review

Abstract

EMBO J 31 8, 1879–1892 March 06 2012 Asymmetric cell division and cell cycle length are two fundamental mechanisms that influence the fate of neural stem cells during mammalian brain development. In this issue of The EMBO Journal, the team of Noriko Osumi proposes an elegant link between the two by showing that the mRNA of cyclinD2, a positive regulator of G1 progression, is confined to the basal end-foot of radial glial cells and is asymmetrically distributed upon mitosis to the two resulting daughter cells (Tsunekawa et al, 2012). According to this model, the daughter cell inheriting cyclinD2 mRNA maintains its self-renewal capability, while lengthening of G1 and differentiation would occur in the sibling cell.

Details

Original languageEnglish
Pages (from-to)1850-1852
Number of pages3
JournalThe EMBO journal
Volume31
Issue number8
Publication statusPublished - 18 Apr 2012
Peer-reviewedYes

External IDs

Scopus 84859891441
PubMed 22453337
PubMedCentral PMC3343342

Keywords

Research priority areas of TU Dresden

DFG Classification of Subject Areas according to Review Boards

Keywords

  • Cell Division, Cyclin D2/biosynthesis, Gene Expression Regulation, Humans, Neurons/physiology