关键词: enhancer nonadditive paired runt wingless

Mesh : Animals Blastoderm / embryology metabolism Body Patterning / genetics physiology DNA-Binding Proteins / genetics metabolism Drosophila / embryology genetics metabolism Drosophila Proteins / genetics metabolism Fushi Tarazu Transcription Factors / genetics metabolism Gene Expression Regulation, Developmental / genetics physiology Homeodomain Proteins / genetics metabolism Transcription Factors / genetics metabolism Wnt1 Protein / genetics metabolism

来  源:   DOI:10.1002/dvdy.142   PDF(Sci-hub)

Abstract:
While many developmentally relevant enhancers act in a modular fashion, there is growing evidence for nonadditive interactions between distinct cis-regulatory enhancers. We investigated if nonautonomous enhancer interactions underlie transcription regulation of the Drosophila segment polarity gene, wingless.
We identified two wg enhancers active at the blastoderm stage: wg 3613u, located from -3.6 to -1.3 kb upstream of the wg transcription start site (TSS) and 3046d, located in intron two of the wg gene, from 3.0 to 4.6 kb downstream of the TSS. Genetic experiments confirm that Even Skipped (Eve), Fushi-tarazu (Ftz), Runt, Odd-paired (Opa), Odd-skipped (Odd), and Paired (Prd) contribute to spatially regulated wg expression. Interestingly, there are enhancer specific differences in response to the gain or loss of function of pair-rule gene activity. Although each element recapitulates aspects of wg expression, a composite reporter containing both enhancers more faithfully recapitulates wg regulation than would be predicted from the sum of their individual responses.
These results suggest that the regulation of wg by pair-rule genes involves nonadditive interactions between distinct cis-regulatory enhancers.
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