| Literature DB >> 29576424 |
Natalia Mora1, Carlos Oliva2, Mark Fiers2, Radoslaw Ejsmont3, Alessia Soldano2, Ting-Ting Zhang4, Jiekun Yan2, Annelies Claeys2, Natalie De Geest2, Bassem A Hassan5.
Abstract
The importance of producing the correct numbers of neurons during development is illustrated by both evolutionary enhancement of cognitive capacities in larger brains, and developmental disorders of brain size. In humans, increased neuronal numbers during development is speculated to partly derive from a unique subtype of neural stem cells (NSCs) that undergo a phase of expansion through symmetric self-amplifying divisions before generating neurons. Symmetric amplification also appears to underlie adult neural stem maintenance in the mouse. However, the mechanisms regulating this behavior are unclear. We report the discovery of self-amplifying NSCs in Drosophila and show that they arise by a spatiotemporal conversion of classical self-renewing NSCs. This conversion is regulated by a temporal transition in the expression of proneural transcription factors prior to cell division. We find a causal link between stem cell self-amplification and increased neuronal numbers. We further show that the temporal transcriptional switch controls both stem cell division and subsequent neuronal differentiation.Entities:
Keywords: Drosophila; brain development; inner proliferation center; neural stem cells; optic lobes; proneural genes; self-renewal; symmetric division; transient amplification
Mesh:
Year: 2018 PMID: 29576424 DOI: 10.1016/j.devcel.2018.02.023
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270