Literature DB >> 25344076

Specification of neuronal subtypes by different levels of Hunchback.

Marta Moris-Sanz1, Alicia Estacio-Gómez1, Javier Alvarez-Rivero1, Fernando J Díaz-Benjumea2.   

Abstract

During the development of the central nervous system, neural progenitors generate an enormous number of distinct types of neuron and glial cells by asymmetric division. Intrinsic genetic programs define the combinations of transcription factors that determine the fate of each cell, but the precise mechanisms by which all these factors are integrated at the level of individual cells are poorly understood. Here, we analyzed the specification of the neurons in the ventral nerve cord of Drosophila that express Crustacean cardioactive peptide (CCAP). There are two types of CCAP neurons: interneurons and efferent neurons. We found that both are specified during the Hunchback temporal window of neuroblast 3-5, but are not sibling cells. Further, this temporal window generates two ganglion mother cells that give rise to four neurons, which can be identified by the expression of empty spiracles. We show that the expression of Hunchback in the neuroblast increases over time and provide evidence that the absolute levels of Hunchback expression specify the two different CCAP neuronal fates.
© 2014. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Bursicon; CCAP; Cell fate specification; Central nervous system; Drosophila; Hunchback; Temporal identity factors

Mesh:

Substances:

Year:  2014        PMID: 25344076     DOI: 10.1242/dev.113381

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  10 in total

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Authors:  M Moris-Sanz; A Estacio-Gómez; E Sánchez-Herrero; F J Díaz-Benjumea
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5.  The Hunchback temporal transcription factor establishes, but is not required to maintain, early-born neuronal identity.

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  10 in total

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