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Fig. 2. The temporal series regulates neuroblast potential and termination.
In Drosophila, multipotent neural progenitors called neuroblasts
(NBs) divide asymmetrically to self-renew and to generate progeny that
differentiate into neurons and/or glia. A single neuroblast can sequentially
express a series of temporal transcription factors such as Hunchback (Hb),
Kruppel (Kr), Nubbin (Pdm), Castor (Cas), Seven-up (Svp) and probably others,
yet unknown. Progression through this series during development schedules the
switch from generating Chinmo+ to Broad-complex+ neurons
and also terminates neuroblast division, either via Prospero-dependent cell
cycle exit (Type-I neuroblasts) or Abdominal-A dependent apoptosis (Type-II
neuroblasts). As neuroblasts progress through the temporal series, their
properties alter. For example, indirect feed-forward from an early burst of
Cas, mediated via a long-lasting switch from Dichaete to Grainyhead, is
necessary for the much-later event of termination. Images courtesy of Cedric
Maurange and Alex Gould (NIMR, London, UK).
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