A System of Repressor Gradients Spatially Organizes the Boundaries of Bicoid-Dependent Target Genes
Author(s) -
Hongtao Chen,
Zhe Xu,
Constance Mei,
Danyang Yu,
Stephen Small
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.03.018
Subject(s) - morphogen , drosophila embryogenesis , biology , krüppel , repressor , homeobox , psychological repression , gap gene , microbiology and biotechnology , genetics , embryo , gene , morphogenesis , function (biology) , transcription factor , embryogenesis , gene expression
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.
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