A System of Repressor Gradients Spatially Organizes the Boundaries of Bicoid-Dependent Target Genes

The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent activation mechanisms. Here, we analyze 66 Bcd-dependent regulatory elements and show that their boundaries are positioned primarily by repressiv...

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Published inCell Vol. 149; no. 3; pp. 618 - 629
Main Authors Chen, Hongtao, Xu, Zhe, Mei, Constance, Yu, Danyang, Small, Stephen
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 27.04.2012
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Online AccessGet full text
ISSN0092-8674
1097-4172
1097-4172
DOI10.1016/j.cell.2012.03.018

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Abstract The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent activation mechanisms. Here, we analyze 66 Bcd-dependent regulatory elements and show that their boundaries are positioned primarily by repressive gradients that antagonize Bcd-mediated activation. A major repressor is the pair-rule protein Runt (Run), which is expressed in an opposing gradient and is necessary and sufficient for limiting Bcd-dependent activation. Evidence is presented that Run functions with the maternal repressor Capicua and the gap protein Kruppel as the principal components of a repression system that correctly orders boundaries throughout the anterior half of the embryo. These results put conceptual limits on the Bcd morphogen hypothesis and demonstrate how the Bcd gradient functions within the gene network that patterns the embryo. [Display omitted] ▸ A Runt protein gradient represses Bicoid-dependent activation in Drosophila embryos ▸ Runt and two other repressors spatially position Bicoid target gene boundaries ▸ At least one repressor binds directly to all 66 known Bicoid-dependent enhancers ▸ The repression system puts conceptual limits on the Bicoid morphogen hypothesis The Bicoid morphogen gradient cannot by itself specify all of the gene expression boundaries of its targets in developing fly embryos. At least three repressors, which bind Bicoid enhancers to antagonize Bicoid target genes, are also required for the formation of well-separated boundaries.
AbstractList The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent activation mechanisms. Here, we analyze 66 Bcd-dependent regulatory elements and show that their boundaries are positioned primarily by repressive gradients that antagonize Bcd-mediated activation. A major repressor is the pair-rule protein Runt (Run), which is expressed in an opposing gradient and is necessary and sufficient for limiting Bcd-dependent activation. Evidence is presented that Run functions with the maternal repressor Capicua and the gap protein Kruppel as the principal components of a repression system that correctly orders boundaries throughout the anterior half of the embryo. These results put conceptual limits on the Bcd morphogen hypothesis and demonstrate how the Bcd gradient functions within the gene network that patterns the embryo.The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent activation mechanisms. Here, we analyze 66 Bcd-dependent regulatory elements and show that their boundaries are positioned primarily by repressive gradients that antagonize Bcd-mediated activation. A major repressor is the pair-rule protein Runt (Run), which is expressed in an opposing gradient and is necessary and sufficient for limiting Bcd-dependent activation. Evidence is presented that Run functions with the maternal repressor Capicua and the gap protein Kruppel as the principal components of a repression system that correctly orders boundaries throughout the anterior half of the embryo. These results put conceptual limits on the Bcd morphogen hypothesis and demonstrate how the Bcd gradient functions within the gene network that patterns the embryo.
The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent activation mechanisms. Here, we analyze 66 Bcd-dependent regulatory elements and show that their boundaries are positioned primarily by repressive gradients that antagonize Bcd-mediated activation. A major repressor is the pair-rule protein Runt (Run), which is expressed in an opposing gradient and is necessary and sufficient for limiting Bcd-dependent activation. Evidence is presented that Run functions with the maternal repressor Capicua and the gap protein Kruppel as the principal components of a repression system that correctly orders boundaries throughout the anterior half of the embryo. These results put conceptual limits on the Bcd morphogen hypothesis and demonstrate how the Bcd gradient functions within the gene network that patterns the embryo.
The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent activation mechanisms. Here, we analyze 66 Bcd-dependent regulatory elements and show that their boundaries are positioned primarily by repressive gradients that antagonize Bcd-mediated activation. A major repressor is the pair-rule protein Runt (Run), which is expressed in an opposing gradient and is necessary and sufficient for limiting Bcd-dependent activation. Evidence is presented that Run functions with the maternal repressor Capicua and the gap protein Kruppel as the principal components of a repression system that correctly orders boundaries throughout the anterior half of the embryo. These results put conceptual limits on the Bcd morphogen hypothesis and demonstrate how the Bcd gradient functions within the gene network that patterns the embryo. [Display omitted] ▸ A Runt protein gradient represses Bicoid-dependent activation in Drosophila embryos ▸ Runt and two other repressors spatially position Bicoid target gene boundaries ▸ At least one repressor binds directly to all 66 known Bicoid-dependent enhancers ▸ The repression system puts conceptual limits on the Bicoid morphogen hypothesis The Bicoid morphogen gradient cannot by itself specify all of the gene expression boundaries of its targets in developing fly embryos. At least three repressors, which bind Bicoid enhancers to antagonize Bicoid target genes, are also required for the formation of well-separated boundaries.
Author Chen, Hongtao
Xu, Zhe
Mei, Constance
Yu, Danyang
Small, Stephen
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  givenname: Zhe
  surname: Xu
  fullname: Xu, Zhe
  organization: Department of Biology, New York University, 100 Washington Square East, New York, NY 10003, USA
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  givenname: Constance
  surname: Mei
  fullname: Mei, Constance
  organization: Department of Biology, New York University, 100 Washington Square East, New York, NY 10003, USA
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  givenname: Danyang
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  organization: Department of Biology, New York University, 100 Washington Square East, New York, NY 10003, USA
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  givenname: Stephen
  surname: Small
  fullname: Small, Stephen
  email: sjs1@nyu.edu
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/22541432$$D View this record in MEDLINE/PubMed
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Snippet The homeodomain (HD) protein Bicoid (Bcd) is thought to function as a gradient morphogen that positions boundaries of target genes via threshold-dependent...
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SubjectTerms Animals
Body Patterning
DNA-Binding Proteins - metabolism
Drosophila melanogaster - embryology
Drosophila melanogaster - genetics
Drosophila melanogaster - metabolism
Drosophila Proteins - metabolism
embryo (animal)
Enhancer Elements, Genetic
Gene Expression Regulation, Developmental
genes
GTPase-activating proteins
homeodomain proteins
Homeodomain Proteins - metabolism
morphogenesis
Nuclear Proteins - metabolism
Trans-Activators - metabolism
Transcription Factors - metabolism
Title A System of Repressor Gradients Spatially Organizes the Boundaries of Bicoid-Dependent Target Genes
URI https://dx.doi.org/10.1016/j.cell.2012.03.018
https://www.ncbi.nlm.nih.gov/pubmed/22541432
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https://www.proquest.com/docview/2000039970
Volume 149
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