Source:http://linkedlifedata.com/resource/pubmed/id/20673828
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-9-24
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pubmed:abstractText |
Subdivision of the neuroectoderm into discrete gene expression domains is essential for the correct specification of neural stem cells (neuroblasts) during central nervous system development. Here, we extend our knowledge on dorsoventral (DV) patterning of the Drosophila brain and uncover novel genetic interactions that control expression of the evolutionary conserved homeobox genes ventral nervous system defective (vnd), intermediate neuroblasts defective (ind), and muscle segment homeobox (msh). We show that cross-repression between Ind and Msh stabilizes the border between intermediate and dorsal tritocerebrum and deutocerebrum, and that both transcription factors are competent to inhibit vnd expression. Conversely, Vnd segment-specifically affects ind expression; it represses ind in the tritocerebrum but positively regulates ind in the deutocerebrum by suppressing Msh. These data provide further evidence that in the brain, in contrast to the trunc, the precise boundaries between DV gene expression domains are largely established through mutual inhibition. Moreover, we find that the segment-polarity gene engrailed (en) regulates the expression of vnd, ind, and msh in a segment-specific manner. En represses msh and ind but maintains vnd expression in the deutocerebrum, is required for down-regulation of Msh in the tritocerebrum to allow activation of ind, and is necessary for maintenance of Ind in truncal segments. These results indicate that input from the anteroposterior patterning system is needed for the spatially restricted expression of DV genes in the brain and ventral nerve cord.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Drop protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/engrail protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/intermediate neuroblasts defective...,
http://linkedlifedata.com/resource/pubmed/chemical/vnd protein, Drosophila
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1095-564X
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
346
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
332-45
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pubmed:meshHeading |
pubmed-meshheading:20673828-Animals,
pubmed-meshheading:20673828-Anterior Horn Cells,
pubmed-meshheading:20673828-Body Patterning,
pubmed-meshheading:20673828-Brain,
pubmed-meshheading:20673828-Drosophila,
pubmed-meshheading:20673828-Drosophila Proteins,
pubmed-meshheading:20673828-Embryo, Nonmammalian,
pubmed-meshheading:20673828-Homeodomain Proteins,
pubmed-meshheading:20673828-Transcription Factors
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pubmed:year |
2010
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pubmed:articleTitle |
Role of en and novel interactions between msh, ind, and vnd in dorsoventral patterning of the Drosophila brain and ventral nerve cord.
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pubmed:affiliation |
Institute of Genetics, University of Mainz, D-55099 Mainz, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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