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The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat
BACKGROUND: Asymmetric somatic hybridization is an efficient crop breeding approach by introducing several exogenous chromatin fragments, which leads to genomic shock and therefore induces genome-wide genetic variation. However, the fundamental question concerning the genetic variation such as wheth...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192298/ https://www.ncbi.nlm.nih.gov/pubmed/30332989 http://dx.doi.org/10.1186/s12870-018-1474-3 |
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author | Wang, Mengcheng Ji, Yujie Feng, Shiting Liu, Chun Xiao, Zhen Wang, Xiaoping Wang, Yanxia Xia, Guangmin |
author_facet | Wang, Mengcheng Ji, Yujie Feng, Shiting Liu, Chun Xiao, Zhen Wang, Xiaoping Wang, Yanxia Xia, Guangmin |
author_sort | Wang, Mengcheng |
collection | PubMed |
description | BACKGROUND: Asymmetric somatic hybridization is an efficient crop breeding approach by introducing several exogenous chromatin fragments, which leads to genomic shock and therefore induces genome-wide genetic variation. However, the fundamental question concerning the genetic variation such as whether it occurs randomly and suffers from selection pressure remains unknown. RESULTS: Here, we explored this issue by comparing expressed sequence tags of a common wheat cultivar and its asymmetric somatic hybrid line. Both nucleotide substitutions and indels (insertions and deletions) had lower frequencies in coding sequences than in un-translated regions. The frequencies of nucleotide substitutions and indels were both comparable between chromosomes with and without introgressed fragments. Nucleotide substitutions distributed unevenly and were preferential to indel-flanking sequences, and the frequency of nucleotide substitutions at 5′-flanking sequences of indels was obviously higher in chromosomes with introgressed fragments than in those without exogenous fragment. Nucleotide substitutions and indels both had various frequencies among seven groups of allelic chromosomes, and the frequencies of nucleotide substitutions were strongly negatively correlative to those of indels. Among three sets of genomes, the frequencies of nucleotide substitutions and indels were both heterogeneous, and the frequencies of nucleotide substitutions exhibited drastically positive correlation to those of indels. CONCLUSIONS: Our work demonstrates that the genetic variation induced by asymmetric somatic hybridization is attributed to both whole genomic shock and local chromosomal shock, which is a predetermined and non-random genetic event being closely associated with selection pressure. Asymmetric somatic hybrids provide a worthwhile model to further investigate the nature of genomic shock induced genetic variation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1474-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6192298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61922982018-10-22 The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat Wang, Mengcheng Ji, Yujie Feng, Shiting Liu, Chun Xiao, Zhen Wang, Xiaoping Wang, Yanxia Xia, Guangmin BMC Plant Biol Research Article BACKGROUND: Asymmetric somatic hybridization is an efficient crop breeding approach by introducing several exogenous chromatin fragments, which leads to genomic shock and therefore induces genome-wide genetic variation. However, the fundamental question concerning the genetic variation such as whether it occurs randomly and suffers from selection pressure remains unknown. RESULTS: Here, we explored this issue by comparing expressed sequence tags of a common wheat cultivar and its asymmetric somatic hybrid line. Both nucleotide substitutions and indels (insertions and deletions) had lower frequencies in coding sequences than in un-translated regions. The frequencies of nucleotide substitutions and indels were both comparable between chromosomes with and without introgressed fragments. Nucleotide substitutions distributed unevenly and were preferential to indel-flanking sequences, and the frequency of nucleotide substitutions at 5′-flanking sequences of indels was obviously higher in chromosomes with introgressed fragments than in those without exogenous fragment. Nucleotide substitutions and indels both had various frequencies among seven groups of allelic chromosomes, and the frequencies of nucleotide substitutions were strongly negatively correlative to those of indels. Among three sets of genomes, the frequencies of nucleotide substitutions and indels were both heterogeneous, and the frequencies of nucleotide substitutions exhibited drastically positive correlation to those of indels. CONCLUSIONS: Our work demonstrates that the genetic variation induced by asymmetric somatic hybridization is attributed to both whole genomic shock and local chromosomal shock, which is a predetermined and non-random genetic event being closely associated with selection pressure. Asymmetric somatic hybrids provide a worthwhile model to further investigate the nature of genomic shock induced genetic variation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1474-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-17 /pmc/articles/PMC6192298/ /pubmed/30332989 http://dx.doi.org/10.1186/s12870-018-1474-3 Text en © The Author(s). 2018 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 Wang, Mengcheng Ji, Yujie Feng, Shiting Liu, Chun Xiao, Zhen Wang, Xiaoping Wang, Yanxia Xia, Guangmin The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
title | The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
title_full | The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
title_fullStr | The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
title_full_unstemmed | The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
title_short | The non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
title_sort | non-random patterns of genetic variation induced by asymmetric somatic hybridization in wheat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192298/ https://www.ncbi.nlm.nih.gov/pubmed/30332989 http://dx.doi.org/10.1186/s12870-018-1474-3 |
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