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Transversions have larger regulatory effects than transitions

BACKGROUND: Transversions (Tv’s) are more likely to alter the amino acid sequence of proteins than transitions (Ts’s), and local deviations in the Ts:Tv ratio are indicative of evolutionary selection on genes. Whether the two different types of mutations have different effects in non-protein-coding...

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Autores principales: Guo, Cong, McDowell, Ian C., Nodzenski, Michael, Scholtens, Denise M., Allen, Andrew S., Lowe, William L., Reddy, Timothy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438547/
https://www.ncbi.nlm.nih.gov/pubmed/28525990
http://dx.doi.org/10.1186/s12864-017-3785-4
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author Guo, Cong
McDowell, Ian C.
Nodzenski, Michael
Scholtens, Denise M.
Allen, Andrew S.
Lowe, William L.
Reddy, Timothy E.
author_facet Guo, Cong
McDowell, Ian C.
Nodzenski, Michael
Scholtens, Denise M.
Allen, Andrew S.
Lowe, William L.
Reddy, Timothy E.
author_sort Guo, Cong
collection PubMed
description BACKGROUND: Transversions (Tv’s) are more likely to alter the amino acid sequence of proteins than transitions (Ts’s), and local deviations in the Ts:Tv ratio are indicative of evolutionary selection on genes. Whether the two different types of mutations have different effects in non-protein-coding sequences remains unknown. Genetic variants primarily impact gene expression by disrupting the binding of transcription factors (TFs) and other DNA-binding proteins. Because Tv’s cause larger changes in the shape of a DNA backbone, we hypothesized that Tv’s would have larger impacts on TF binding and gene expression. RESULTS: Here, we provide multiple lines of evidence demonstrating that Tv’s have larger impacts on regulatory DNA including analyses of TF binding motifs and allele-specific TF binding. In these analyses, we observed a depletion of Tv’s within TF binding motifs and TF binding sites. Using massively parallel population-scale reporter assays, we also provided empirical evidence that Tv’s have larger effects than Ts’s on the activity of human gene regulatory elements. CONCLUSIONS: Tv’s are more likely to disrupt TF binding, resulting in larger changes in gene expression. Although the observed differences are small, these findings represent a novel, fundamental property of regulatory variation. Understanding the features of functional non-coding variation could be valuable for revealing the genetic underpinnings of complex traits and diseases in future studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3785-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-54385472017-05-22 Transversions have larger regulatory effects than transitions Guo, Cong McDowell, Ian C. Nodzenski, Michael Scholtens, Denise M. Allen, Andrew S. Lowe, William L. Reddy, Timothy E. BMC Genomics Research Article BACKGROUND: Transversions (Tv’s) are more likely to alter the amino acid sequence of proteins than transitions (Ts’s), and local deviations in the Ts:Tv ratio are indicative of evolutionary selection on genes. Whether the two different types of mutations have different effects in non-protein-coding sequences remains unknown. Genetic variants primarily impact gene expression by disrupting the binding of transcription factors (TFs) and other DNA-binding proteins. Because Tv’s cause larger changes in the shape of a DNA backbone, we hypothesized that Tv’s would have larger impacts on TF binding and gene expression. RESULTS: Here, we provide multiple lines of evidence demonstrating that Tv’s have larger impacts on regulatory DNA including analyses of TF binding motifs and allele-specific TF binding. In these analyses, we observed a depletion of Tv’s within TF binding motifs and TF binding sites. Using massively parallel population-scale reporter assays, we also provided empirical evidence that Tv’s have larger effects than Ts’s on the activity of human gene regulatory elements. CONCLUSIONS: Tv’s are more likely to disrupt TF binding, resulting in larger changes in gene expression. Although the observed differences are small, these findings represent a novel, fundamental property of regulatory variation. Understanding the features of functional non-coding variation could be valuable for revealing the genetic underpinnings of complex traits and diseases in future studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3785-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-19 /pmc/articles/PMC5438547/ /pubmed/28525990 http://dx.doi.org/10.1186/s12864-017-3785-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Guo, Cong
McDowell, Ian C.
Nodzenski, Michael
Scholtens, Denise M.
Allen, Andrew S.
Lowe, William L.
Reddy, Timothy E.
Transversions have larger regulatory effects than transitions
title Transversions have larger regulatory effects than transitions
title_full Transversions have larger regulatory effects than transitions
title_fullStr Transversions have larger regulatory effects than transitions
title_full_unstemmed Transversions have larger regulatory effects than transitions
title_short Transversions have larger regulatory effects than transitions
title_sort transversions have larger regulatory effects than transitions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438547/
https://www.ncbi.nlm.nih.gov/pubmed/28525990
http://dx.doi.org/10.1186/s12864-017-3785-4
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