CyclinD2 at the edge: splitting up cell fate
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
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 language | English |
---|---|
Pages (from-to) | 1850-1852 |
Number of pages | 3 |
Journal | The EMBO journal |
Volume | 31 |
Issue number | 8 |
Publication status | Published - 18 Apr 2012 |
Peer-reviewed | Yes |
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