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Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation
Dosage compensation is an essential process that equalizes transcript levels of X-linked genes between sexes by forming a domain of coordinated gene expression. Throughout the evolution of Diptera, many different X-chromosomes acquired the ability to be dosage compensated. Once each newly evolved X-...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945028/ https://www.ncbi.nlm.nih.gov/pubmed/27414415 http://dx.doi.org/10.1371/journal.pgen.1006120 |
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author | Kuzu, Guray Kaye, Emily G. Chery, Jessica Siggers, Trevor Yang, Lin Dobson, Jason R. Boor, Sonia Bliss, Jacob Liu, Wei Jogl, Gerwald Rohs, Remo Singh, Nadia D. Bulyk, Martha L. Tolstorukov, Michael Y. Larschan, Erica |
author_facet | Kuzu, Guray Kaye, Emily G. Chery, Jessica Siggers, Trevor Yang, Lin Dobson, Jason R. Boor, Sonia Bliss, Jacob Liu, Wei Jogl, Gerwald Rohs, Remo Singh, Nadia D. Bulyk, Martha L. Tolstorukov, Michael Y. Larschan, Erica |
author_sort | Kuzu, Guray |
collection | PubMed |
description | Dosage compensation is an essential process that equalizes transcript levels of X-linked genes between sexes by forming a domain of coordinated gene expression. Throughout the evolution of Diptera, many different X-chromosomes acquired the ability to be dosage compensated. Once each newly evolved X-chromosome is targeted for dosage compensation in XY males, its active genes are upregulated two-fold to equalize gene expression with XX females. In Drosophila melanogaster, the CLAMP zinc finger protein links the dosage compensation complex to the X-chromosome. However, the mechanism for X-chromosome identification has remained unknown. Here, we combine biochemical, genomic and evolutionary approaches to reveal that expansion of GA-dinucleotide repeats likely accumulated on the X-chromosome over evolutionary time to increase the density of CLAMP binding sites, thereby driving the evolution of dosage compensation. Overall, we present new insight into how subtle changes in genomic architecture, such as expansions of a simple sequence repeat, promote the evolution of coordinated gene expression. |
format | Online Article Text |
id | pubmed-4945028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49450282016-08-08 Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation Kuzu, Guray Kaye, Emily G. Chery, Jessica Siggers, Trevor Yang, Lin Dobson, Jason R. Boor, Sonia Bliss, Jacob Liu, Wei Jogl, Gerwald Rohs, Remo Singh, Nadia D. Bulyk, Martha L. Tolstorukov, Michael Y. Larschan, Erica PLoS Genet Research Article Dosage compensation is an essential process that equalizes transcript levels of X-linked genes between sexes by forming a domain of coordinated gene expression. Throughout the evolution of Diptera, many different X-chromosomes acquired the ability to be dosage compensated. Once each newly evolved X-chromosome is targeted for dosage compensation in XY males, its active genes are upregulated two-fold to equalize gene expression with XX females. In Drosophila melanogaster, the CLAMP zinc finger protein links the dosage compensation complex to the X-chromosome. However, the mechanism for X-chromosome identification has remained unknown. Here, we combine biochemical, genomic and evolutionary approaches to reveal that expansion of GA-dinucleotide repeats likely accumulated on the X-chromosome over evolutionary time to increase the density of CLAMP binding sites, thereby driving the evolution of dosage compensation. Overall, we present new insight into how subtle changes in genomic architecture, such as expansions of a simple sequence repeat, promote the evolution of coordinated gene expression. Public Library of Science 2016-07-14 /pmc/articles/PMC4945028/ /pubmed/27414415 http://dx.doi.org/10.1371/journal.pgen.1006120 Text en © 2016 Kuzu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kuzu, Guray Kaye, Emily G. Chery, Jessica Siggers, Trevor Yang, Lin Dobson, Jason R. Boor, Sonia Bliss, Jacob Liu, Wei Jogl, Gerwald Rohs, Remo Singh, Nadia D. Bulyk, Martha L. Tolstorukov, Michael Y. Larschan, Erica Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation |
title | Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation |
title_full | Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation |
title_fullStr | Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation |
title_full_unstemmed | Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation |
title_short | Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation |
title_sort | expansion of ga dinucleotide repeats increases the density of clamp binding sites on the x-chromosome to promote drosophila dosage compensation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945028/ https://www.ncbi.nlm.nih.gov/pubmed/27414415 http://dx.doi.org/10.1371/journal.pgen.1006120 |
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