Literature DB >> 2797168

Mutant Drosophila embryos in which all cells adopt a neural fate.

M Bourouis1, P Heitzler, M el Messal, P Simpson.   

Abstract

In the Drosophila embryo, early developmental decisions lead to all cells adopting one of several initial fates, such as those characteristic of the germ layers. The central nervous system is formed subsequently from the neurogenic region of the ectoderm, in which progenitor cells of the neuroblasts and ventral epidermis are intermingled. Two classes of genes govern the segregation of neuroblasts and peripheral sensory organs. The pro-neural class of genes, for example, the achaete-scute complex, participates in the initial decision to make each uniquely positioned neuroblast or sensory organ, but are initially expressed in groups of cells. The segregation of a neuroblast or sensory organ from an equivalent group of equipotential cells involves a mechanism of lateral inhibition whereby the future epidermal cells are prevented from engaging in the primary dominant neural fate. In the absence of this inhibitory signal, all cells of the group will become neural by default. The neurogenic class of genes is thought to mediate these cell interactions. Here we report that cells in embryos mutant for shaggy which are unable to adopt any of the early initial fates, instead develop neural characteristics.

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Year:  1989        PMID: 2797168     DOI: 10.1038/341442a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  9 in total

1.  eyelid antagonizes wingless signaling during Drosophila development and has homology to the Bright family of DNA-binding proteins.

Authors:  J E Treisman; A Luk; G M Rubin; U Heberlein
Journal:  Genes Dev       Date:  1997-08-01       Impact factor: 11.361

2.  Arabidopsis homologs of the shaggy and GSK-3 protein kinases: molecular cloning and functional expression in Escherichia coli.

Authors:  M W Bianchi; D Guivarc'h; M Thomas; J R Woodgett; M Kreis
Journal:  Mol Gen Genet       Date:  1994-02

3.  Shaggy/glycogen synthase kinase 3β and phosphorylation of Sarah/regulator of calcineurin are essential for completion of Drosophila female meiosis.

Authors:  Satomi Takeo; Selene K Swanson; Kavyasree Nandanan; Yasuhiro Nakai; Toshiro Aigaki; Michael P Washburn; Laurence Florens; R Scott Hawley
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-15       Impact factor: 11.205

4.  Intralineage directional Notch signaling regulates self-renewal and differentiation of asymmetrically dividing radial glia.

Authors:  Zhiqiang Dong; Nan Yang; Sang-Yeob Yeo; Ajay Chitnis; Su Guo
Journal:  Neuron       Date:  2012-04-12       Impact factor: 17.173

5.  Ribosomal s6 kinase cooperates with casein kinase 2 to modulate the Drosophila circadian molecular oscillator.

Authors:  Bikem Akten; Michelle M Tangredi; Eike Jauch; Mary A Roberts; Fanny Ng; Thomas Raabe; F Rob Jackson
Journal:  J Neurosci       Date:  2009-01-14       Impact factor: 6.167

6.  Functional studies of shaggy/glycogen synthase kinase 3 phosphorylation sites in Drosophila melanogaster.

Authors:  Deppie Papadopoulou; Michele Wolfe Bianchi; Marc Bourouis
Journal:  Mol Cell Biol       Date:  2004-06       Impact factor: 4.272

7.  An early embryonic product of the gene shaggy encodes a serine/threonine protein kinase related to the CDC28/cdc2+ subfamily.

Authors:  M Bourouis; P Moore; L Ruel; Y Grau; P Heitzler; P Simpson
Journal:  EMBO J       Date:  1990-09       Impact factor: 11.598

8.  Functional significance of a family of protein kinases encoded at the shaggy locus in Drosophila.

Authors:  L Ruel; V Pantesco; Y Lutz; P Simpson; M Bourouis
Journal:  EMBO J       Date:  1993-04       Impact factor: 11.598

Review 9.  Powerful Drosophila screens that paved the wingless pathway.

Authors:  Fabian Heinz Jenny; Konrad Basler
Journal:  Fly (Austin)       Date:  2015-01-20       Impact factor: 2.160

  9 in total

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