Literature DB >> 11546742

Successive specification of Drosophila neuroblasts NB 6-4 and NB 7-3 depends on interaction of the segment polarity genes wingless, gooseberry and naked cuticle.

N Deshpande1, R Dittrich, G M Technau, J Urban.   

Abstract

The Drosophila central nervous system derives from neural precursor cells, the neuroblasts (NBs), which are born from the neuroectoderm by the process of delamination. Each NB has a unique identity, which is revealed by the production of a characteristic cell lineage and a specific set of molecular markers it expresses. These NBs delaminate at different but reproducible time points during neurogenesis (S1-S5) and it has been shown for early delaminating NBs (S1/S2) that their identities depend on positional information conferred by segment polarity genes and dorsoventral patterning genes. We have studied mechanisms leading to the fate specification of a set of late delaminating neuroblasts, NB 6-4 and NB 7-3, both of which arise from the engrailed (en) expression domain, with NB 6-4 delaminating first. In contrast to former reports, we did not find any evidence for a direct role of hedgehog in the process of NB 7-3 specification. Instead, we present evidence to show that the interplay of the segmentation genes naked cuticle (nkd) and gooseberry (gsb), both of which are targets of wingless (wg) activity, leads to differential commitment to NB 6-4 and NB 7-3 cell fate. In the absence of either nkd or gsb, one NB fate is replaced by the other. However, the temporal sequence of delamination is maintained, suggesting that formation and specification of these two NBs are under independent control.

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Year:  2001        PMID: 11546742     DOI: 10.1242/dev.128.17.3253

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


  12 in total

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Authors:  Steffen Harzsch; Carsten H G Müller; Harald Wolf
Journal:  Dev Genes Evol       Date:  2004-12-09       Impact factor: 0.900

2.  Synaptic homeostasis is consolidated by the cell fate gene gooseberry, a Drosophila pax3/7 homolog.

Authors:  Bruno Marie; Edward Pym; Sharon Bergquist; Graeme W Davis
Journal:  J Neurosci       Date:  2010-06-16       Impact factor: 6.167

3.  Differentiation of the Drosophila serotonergic lineage depends on the regulation of Zfh-1 by Notch and Eagle.

Authors:  Hyung-Kook Lee; Martha J Lundell
Journal:  Mol Cell Neurosci       Date:  2007-07-21       Impact factor: 4.314

4.  Integrated Patterning Programs During Drosophila Development Generate the Diversity of Neurons and Control Their Mature Properties.

Authors:  Anthony M Rossi; Shadi Jafari; Claude Desplan
Journal:  Annu Rev Neurosci       Date:  2021-02-08       Impact factor: 12.449

5.  Functional conservation of the Drosophila gooseberry gene and its evolutionary alleles.

Authors:  Wei Liu; Lei Xue
Journal:  PLoS One       Date:  2012-01-23       Impact factor: 3.240

6.  The RED domain of Paired is specifically required for Drosophila accessory gland maturation.

Authors:  Li Li; Ping Li; Lei Xue
Journal:  Open Biol       Date:  2015-02       Impact factor: 6.411

7.  Genetic transformation of structural and functional circuitry rewires the Drosophila brain.

Authors:  Sonia Sen; Deshou Cao; Ramveer Choudhary; Silvia Biagini; Jing W Wang; Heinrich Reichert; K VijayRaghavan
Journal:  Elife       Date:  2014-12-29       Impact factor: 8.140

8.  Cell-Autonomous and Non-cell-autonomous Function of Hox Genes Specify Segmental Neuroblast Identity in the Gnathal Region of the Embryonic CNS in Drosophila.

Authors:  Henrike Becker; Simone Renner; Gerhard M Technau; Christian Berger
Journal:  PLoS Genet       Date:  2016-03-25       Impact factor: 5.917

9.  Embryonic origins of a motor system: motor dendrites form a myotopic map in Drosophila.

Authors:  Matthias Landgraf; Victoria Jeffrey; Miki Fujioka; James B Jaynes; Michael Bate
Journal:  PLoS Biol       Date:  2003-11-17       Impact factor: 8.029

10.  A concerted action of Engrailed and Gooseberry-Neuro in neuroblast 6-4 is triggering the formation of embryonic posterior commissure bundles.

Authors:  Sophie Colomb; Willy Joly; Nathalie Bonneaud; Florence Maschat
Journal:  PLoS One       Date:  2008-05-21       Impact factor: 3.240

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