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Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex

Chromatin boundary elements subdivide chromosomes in multicellular organisms into physically independent domains. In addition to this architectural function, these elements also play a critical role in gene regulation. Here we investigated the evolution of a Drosophila Bithorax complex boundary elem...

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Autores principales: Cleard, Fabienne, Wolle, Daniel, Taverner, Andrew M., Aoki, Tsutomu, Deshpande, Girish, Andolfatto, Peter, Karch, Francois, Schedl, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289839/
https://www.ncbi.nlm.nih.gov/pubmed/28007886
http://dx.doi.org/10.1534/genetics.116.195586
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author Cleard, Fabienne
Wolle, Daniel
Taverner, Andrew M.
Aoki, Tsutomu
Deshpande, Girish
Andolfatto, Peter
Karch, Francois
Schedl, Paul
author_facet Cleard, Fabienne
Wolle, Daniel
Taverner, Andrew M.
Aoki, Tsutomu
Deshpande, Girish
Andolfatto, Peter
Karch, Francois
Schedl, Paul
author_sort Cleard, Fabienne
collection PubMed
description Chromatin boundary elements subdivide chromosomes in multicellular organisms into physically independent domains. In addition to this architectural function, these elements also play a critical role in gene regulation. Here we investigated the evolution of a Drosophila Bithorax complex boundary element called Fab-7, which is required for the proper parasegment specific expression of the homeotic Abd-B gene. Using a “gene” replacement strategy, we show that Fab-7 boundaries from two closely related species, D. erecta and D. yakuba, and a more distant species, D. pseudoobscura, are able to substitute for the melanogaster boundary. Consistent with this functional conservation, the two known Fab-7 boundary factors, Elba and LBC, have recognition sequences in the boundaries from all species. However, the strategies used for maintaining binding and function in the face of sequence divergence is different. The first is conventional, and depends upon conservation of the 8 bp Elba recognition sequence. The second is unconventional, and takes advantage of the unusually large and flexible sequence recognition properties of the LBC boundary factor, and the deployment of multiple LBC recognition elements in each boundary. In the former case, binding is lost when the recognition sequence is altered. In the latter case, sequence divergence is accompanied by changes in the number, relative affinity, and location of the LBC recognition elements.
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spelling pubmed-52898392017-02-10 Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex Cleard, Fabienne Wolle, Daniel Taverner, Andrew M. Aoki, Tsutomu Deshpande, Girish Andolfatto, Peter Karch, Francois Schedl, Paul Genetics Investigations Chromatin boundary elements subdivide chromosomes in multicellular organisms into physically independent domains. In addition to this architectural function, these elements also play a critical role in gene regulation. Here we investigated the evolution of a Drosophila Bithorax complex boundary element called Fab-7, which is required for the proper parasegment specific expression of the homeotic Abd-B gene. Using a “gene” replacement strategy, we show that Fab-7 boundaries from two closely related species, D. erecta and D. yakuba, and a more distant species, D. pseudoobscura, are able to substitute for the melanogaster boundary. Consistent with this functional conservation, the two known Fab-7 boundary factors, Elba and LBC, have recognition sequences in the boundaries from all species. However, the strategies used for maintaining binding and function in the face of sequence divergence is different. The first is conventional, and depends upon conservation of the 8 bp Elba recognition sequence. The second is unconventional, and takes advantage of the unusually large and flexible sequence recognition properties of the LBC boundary factor, and the deployment of multiple LBC recognition elements in each boundary. In the former case, binding is lost when the recognition sequence is altered. In the latter case, sequence divergence is accompanied by changes in the number, relative affinity, and location of the LBC recognition elements. Genetics Society of America 2017-02 2016-12-20 /pmc/articles/PMC5289839/ /pubmed/28007886 http://dx.doi.org/10.1534/genetics.116.195586 Text en Copyright © 2017 by the Genetics Society of America Available freely online through the author-supported open access option.
spellingShingle Investigations
Cleard, Fabienne
Wolle, Daniel
Taverner, Andrew M.
Aoki, Tsutomu
Deshpande, Girish
Andolfatto, Peter
Karch, Francois
Schedl, Paul
Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex
title Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex
title_full Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex
title_fullStr Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex
title_full_unstemmed Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex
title_short Different Evolutionary Strategies To Conserve Chromatin Boundary Function in the Bithorax Complex
title_sort different evolutionary strategies to conserve chromatin boundary function in the bithorax complex
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289839/
https://www.ncbi.nlm.nih.gov/pubmed/28007886
http://dx.doi.org/10.1534/genetics.116.195586
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