Literature DB >> 20040486

Drosophila Hey is a target of Notch in asymmetric divisions during embryonic and larval neurogenesis.

Maria Monastirioti1, Nikolaos Giagtzoglou, Konstantinos A Koumbanakis, Evanthia Zacharioudaki, Myrto Deligiannaki, Irmgard Wech, Mara Almeida, Anette Preiss, Sarah Bray, Christos Delidakis.   

Abstract

bHLH-O proteins are a subfamily of the basic-helix-loop-helix transcription factors characterized by an 'Orange' protein-protein interaction domain. Typical members are the Hairy/E(spl), or Hes, proteins, well studied in their ability, among others, to suppress neuronal differentiation in both invertebrates and vertebrates. Hes proteins are often effectors of Notch signalling. In vertebrates, another bHLH-O protein group, the Hey proteins, have also been shown to be Notch targets and to interact with Hes. We have studied the single Drosophila Hey orthologue. We show that it is primarily expressed in a subset of newly born neurons, which receive Notch signalling during their birth. Unlike in vertebrates, however, Hey is not expressed in precursor cells and does not block neuronal differentiation. It rather promotes one of two alternative fates that sibling neurons adopt at birth. Although in the majority of cases Hey is a Notch target, it is also expressed independently of Notch in some lineages, most notably the larval mushroom body. The availability of Hey as a Notch readout has allowed us to study Notch signalling during the genesis of secondary neurons in the larval central nervous system.

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Year:  2010        PMID: 20040486      PMCID: PMC2799155          DOI: 10.1242/dev.043604

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


  61 in total

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Journal:  Development       Date:  2005-08-10       Impact factor: 6.868

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  25 in total

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3.  Dynamic regulation of mRNA decay during neural development.

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4.  Temporal patterning of neuroblasts controls Notch-mediated cell survival through regulation of Hid or Reaper.

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6.  Aging Neural Progenitors Lose Competence to Respond to Mitogenic Notch Signaling.

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8.  Genome-wide association study of sleep in Drosophila melanogaster.

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Journal:  BMC Genomics       Date:  2013-04-25       Impact factor: 3.969

9.  Uncovering the link between malfunctions in Drosophila neuroblast asymmetric cell division and tumorigenesis.

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10.  Lineage analysis of Drosophila lateral antennal lobe neurons reveals notch-dependent binary temporal fate decisions.

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