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Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean
BACKGROUND: Plant domestication provides a unique model to study genome evolution. Many studies have been conducted to examine genes, genetic diversity, genome structure, and epigenome changes associated with domestication. Interestingly, domesticated accessions have significantly higher [A] and [T]...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482504/ https://www.ncbi.nlm.nih.gov/pubmed/31018867 http://dx.doi.org/10.1186/s13059-019-1683-6 |
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author | Wang, Jinyu Li, Xianran Do Kim, Kyung Scanlon, Michael J. Jackson, Scott A. Springer, Nathan M. Yu, Jianming |
author_facet | Wang, Jinyu Li, Xianran Do Kim, Kyung Scanlon, Michael J. Jackson, Scott A. Springer, Nathan M. Yu, Jianming |
author_sort | Wang, Jinyu |
collection | PubMed |
description | BACKGROUND: Plant domestication provides a unique model to study genome evolution. Many studies have been conducted to examine genes, genetic diversity, genome structure, and epigenome changes associated with domestication. Interestingly, domesticated accessions have significantly higher [A] and [T] values across genome-wide polymorphic sites than accessions sampled from the corresponding progenitor species. However, the relative contributions of different genomic regions to this genome divergence pattern and underlying mechanisms have not been well characterized. RESULTS: Here, we investigate the genome-wide base-composition patterns by analyzing millions of SNPs segregating among 100 accessions from a teosinte-maize comparison set and among 302 accessions from a wild-domesticated soybean comparison set. We show that non-genic part of the genome has a greater contribution than genic SNPs to the [AT]-increase observed between wild and domesticated accessions in maize and soybean. The separation between wild and domesticated accessions in [AT] values is significantly enlarged in non-genic and pericentromeric regions. Motif frequency and sequence context analyses show the motifs (PyCG) related to solar-UV signature are enriched in these regions, particularly when they are methylated. Additional analysis using population-private SNPs also implicates the role of these motifs in relatively recent mutations. With base-composition across polymorphic sites as a genome phenotype, genome scans identify a set of putative candidate genes involved in UV damage repair pathways. CONCLUSIONS: The [AT]-increase is more pronounced in genomic regions that are non-genic, pericentromeric, transposable elements; methylated; and with low recombination. Our findings establish important links among UV radiation, mutation, DNA repair, methylation, and genome evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1683-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6482504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64825042019-05-02 Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean Wang, Jinyu Li, Xianran Do Kim, Kyung Scanlon, Michael J. Jackson, Scott A. Springer, Nathan M. Yu, Jianming Genome Biol Research BACKGROUND: Plant domestication provides a unique model to study genome evolution. Many studies have been conducted to examine genes, genetic diversity, genome structure, and epigenome changes associated with domestication. Interestingly, domesticated accessions have significantly higher [A] and [T] values across genome-wide polymorphic sites than accessions sampled from the corresponding progenitor species. However, the relative contributions of different genomic regions to this genome divergence pattern and underlying mechanisms have not been well characterized. RESULTS: Here, we investigate the genome-wide base-composition patterns by analyzing millions of SNPs segregating among 100 accessions from a teosinte-maize comparison set and among 302 accessions from a wild-domesticated soybean comparison set. We show that non-genic part of the genome has a greater contribution than genic SNPs to the [AT]-increase observed between wild and domesticated accessions in maize and soybean. The separation between wild and domesticated accessions in [AT] values is significantly enlarged in non-genic and pericentromeric regions. Motif frequency and sequence context analyses show the motifs (PyCG) related to solar-UV signature are enriched in these regions, particularly when they are methylated. Additional analysis using population-private SNPs also implicates the role of these motifs in relatively recent mutations. With base-composition across polymorphic sites as a genome phenotype, genome scans identify a set of putative candidate genes involved in UV damage repair pathways. CONCLUSIONS: The [AT]-increase is more pronounced in genomic regions that are non-genic, pericentromeric, transposable elements; methylated; and with low recombination. Our findings establish important links among UV radiation, mutation, DNA repair, methylation, and genome evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1683-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-25 /pmc/articles/PMC6482504/ /pubmed/31018867 http://dx.doi.org/10.1186/s13059-019-1683-6 Text en © The Author(s). 2019 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 Wang, Jinyu Li, Xianran Do Kim, Kyung Scanlon, Michael J. Jackson, Scott A. Springer, Nathan M. Yu, Jianming Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
title | Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
title_full | Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
title_fullStr | Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
title_full_unstemmed | Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
title_short | Genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
title_sort | genome-wide nucleotide patterns and potential mechanisms of genome divergence following domestication in maize and soybean |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482504/ https://www.ncbi.nlm.nih.gov/pubmed/31018867 http://dx.doi.org/10.1186/s13059-019-1683-6 |
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