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Control of neuronal cell fate and number by integration of distinct daughter cell proliferation modes with temporal progression
Author(s) -
Carina Ulvklo,
Ryan B. MacDonald,
Caroline Bivik Stadler,
Magnus Baumgardt,
Daniel Karlsson,
Stefan Thor
Publication year - 2012
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.074500
Subject(s) - biology , neuroblast , cell division , cell fate determination , daughter , microbiology and biotechnology , cell growth , neural cell , cell , lineage (genetic) , precursor cell , neuroscience , genetics , evolutionary biology , neurogenesis , gene , transcription factor
During neural lineage progression, differences in daughter cell proliferation can generate different lineage topologies. This is apparent in the Drosophila neuroblast 5-6 lineage (NB5-6T), which undergoes a daughter cell proliferation switch from generating daughter cells that divide once to generating neurons directly. Simultaneously, neural lineages, e.g. NB5-6T, undergo temporal changes in competence, as evidenced by the generation of different neural subtypes at distinct time points. When daughter proliferation is altered against a backdrop of temporal competence changes, it may create an integrative mechanism for simultaneously controlling cell fate and number. Here, we identify two independent pathways, Prospero and Notch, which act in concert to control the different daughter cell proliferation modes in NB5-6T. Altering daughter cell proliferation and temporal progression, individually and simultaneously, results in predictable changes in cell fate and number. This demonstrates that different daughter cell proliferation modes can be integrated with temporal competence changes, and suggests a novel mechanism for coordinately controlling neuronal subtype numbers.

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