Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.

Spatial patterning of gene expression is a key process in development, yet how it evolves is still poorly understood. Both cis- and trans-acting changes could participate in complex interactions, so to isolate the cis-regulatory component of patterning evolution, we measured allele-specific spatial...

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Main Authors: Peter A Combs, Hunter B Fraser
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-11-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC6211617?pdf=render
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spelling doaj-f790e5dc62f14d6190c2b2e440b543632020-11-24T21:44:21ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042018-11-011411e100763110.1371/journal.pgen.1007631Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.Peter A CombsHunter B FraserSpatial patterning of gene expression is a key process in development, yet how it evolves is still poorly understood. Both cis- and trans-acting changes could participate in complex interactions, so to isolate the cis-regulatory component of patterning evolution, we measured allele-specific spatial gene expression patterns in D. melanogaster × simulans hybrid embryos. RNA-seq of cryo-sectioned slices revealed 66 genes with strong spatially varying allele-specific expression. We found that hunchback, a major regulator of developmental patterning, had reduced expression of the D. simulans allele specifically in the anterior tip of hybrid embryos. Mathematical modeling of hunchback cis-regulation suggested a candidate transcription factor binding site variant, which we verified as causal using CRISPR-Cas9 genome editing. In sum, even comparing morphologically near-identical species we identified surprisingly extensive spatial variation in gene expression, suggesting not only that development is robust to many such changes, but also that natural selection may have ample raw material for evolving new body plans via changes in spatial patterning.http://europepmc.org/articles/PMC6211617?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Peter A Combs
Hunter B Fraser
spellingShingle Peter A Combs
Hunter B Fraser
Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.
PLoS Genetics
author_facet Peter A Combs
Hunter B Fraser
author_sort Peter A Combs
title Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.
title_short Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.
title_full Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.
title_fullStr Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.
title_full_unstemmed Spatially varying cis-regulatory divergence in Drosophila embryos elucidates cis-regulatory logic.
title_sort spatially varying cis-regulatory divergence in drosophila embryos elucidates cis-regulatory logic.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2018-11-01
description Spatial patterning of gene expression is a key process in development, yet how it evolves is still poorly understood. Both cis- and trans-acting changes could participate in complex interactions, so to isolate the cis-regulatory component of patterning evolution, we measured allele-specific spatial gene expression patterns in D. melanogaster × simulans hybrid embryos. RNA-seq of cryo-sectioned slices revealed 66 genes with strong spatially varying allele-specific expression. We found that hunchback, a major regulator of developmental patterning, had reduced expression of the D. simulans allele specifically in the anterior tip of hybrid embryos. Mathematical modeling of hunchback cis-regulation suggested a candidate transcription factor binding site variant, which we verified as causal using CRISPR-Cas9 genome editing. In sum, even comparing morphologically near-identical species we identified surprisingly extensive spatial variation in gene expression, suggesting not only that development is robust to many such changes, but also that natural selection may have ample raw material for evolving new body plans via changes in spatial patterning.
url http://europepmc.org/articles/PMC6211617?pdf=render
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AT hunterbfraser spatiallyvaryingcisregulatorydivergenceindrosophilaembryoselucidatescisregulatorylogic
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