Literature DB >> 17314131

Cell lineage-specific expression and function of the empty spiracles gene in adult brain development of Drosophila melanogaster.

Robert Lichtneckert1, Bruno Bello, Heinrich Reichert.   

Abstract

The empty spiracles (ems) gene, encoding a homeodomain transcription factor, is a member of the cephalic gap gene family that acts in early specification of the anterior neuroectoderm in the embryonic brain of Drosophila. Here we show that ems is also expressed in the mature adult brain in the lineage-restricted clonal progeny of a single neuroblast in each brain hemisphere. These ems-expressing neuronal cells are located ventral to the antennal lobes and project a fascicle to the superior medial protocerebrum. All adult-specific secondary neurons in this lineage persistently express ems during postembryonic larval development and continue to do so throughout metamorphosis and into the adult. Mosaic-based MARCM mutant analysis and genetic rescue experiments demonstrate that ems function is autonomously required for the correct number of cells in the persistently expressing adult-specific lineage. Moreover, they indicate that ems is also required cell autonomously for the formation of the correct projections in this specific lineage. This analysis of ems expression and function reveals novel and unexpected roles of a cephalic gap gene in translating lineage information into cell number control and projection specificity in an individual clonal unit of the adult brain.

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Year:  2007        PMID: 17314131     DOI: 10.1242/dev.02814

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


  6 in total

1.  Patterns of growth and tract formation during the early development of secondary lineages in the Drosophila larval brain.

Authors:  Jennifer K Lovick; Angel Kong; Jaison J Omoto; Kathy T Ngo; Amelia Younossi-Hartenstein; Volker Hartenstein
Journal:  Dev Neurobiol       Date:  2015-07-28       Impact factor: 3.964

2.  Analysis of neurotransmitter tissue content of Drosophila melanogaster in different life stages.

Authors:  Madelaine E Denno; Eve Privman; B Jill Venton
Journal:  ACS Chem Neurosci       Date:  2014-12-05       Impact factor: 4.418

3.  Making Drosophila lineage-restricted drivers via patterned recombination in neuroblasts.

Authors:  Takeshi Awasaki; Chih-Fei Kao; Ying-Jou Lee; Ching-Po Yang; Yaling Huang; Barret D Pfeiffer; Haojiang Luan; Xiaotang Jing; Yu-Fen Huang; Yisheng He; Mark David Schroeder; Alexander Kuzin; Thomas Brody; Christopher T Zugates; Ward F Odenwald; Tzumin Lee
Journal:  Nat Neurosci       Date:  2014-02-23       Impact factor: 24.884

Review 4.  Power tools for gene expression and clonal analysis in Drosophila.

Authors:  Alberto del Valle Rodríguez; Dominic Didiano; Claude Desplan
Journal:  Nat Methods       Date:  2011-12-28       Impact factor: 28.547

5.  Arborization pattern of engrailed-positive neural lineages reveal neuromere boundaries in the Drosophila brain neuropil.

Authors:  Abhilasha Kumar; S Fung; Robert Lichtneckert; Heinrich Reichert; Volker Hartenstein
Journal:  J Comp Neurol       Date:  2009-11-01       Impact factor: 3.215

6.  Drosophila olfactory local interneurons and projection neurons derive from a common neuroblast lineage specified by the empty spiracles gene.

Authors:  Abhijit Das; Sonia Sen; Robert Lichtneckert; Ryuichi Okada; Kei Ito; Veronica Rodrigues; Heinrich Reichert
Journal:  Neural Dev       Date:  2008-12-03       Impact factor: 3.842

  6 in total

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