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Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula
BACKGROUND: Fast neutron bombardment (FNB) is a very effective approach for mutagenesis and has been widely used in generating mutant libraries in many plant species. The main type of mutations of FNB mutants are deletions of DNA fragments ranging from few base pairs to several hundred kilobases, th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207604/ https://www.ncbi.nlm.nih.gov/pubmed/34134730 http://dx.doi.org/10.1186/s13007-021-00765-y |
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author | Du, Huan Jiao, Zhicheng Liu, Junjie Huang, Wei Ge, Liangfa |
author_facet | Du, Huan Jiao, Zhicheng Liu, Junjie Huang, Wei Ge, Liangfa |
author_sort | Du, Huan |
collection | PubMed |
description | BACKGROUND: Fast neutron bombardment (FNB) is a very effective approach for mutagenesis and has been widely used in generating mutant libraries in many plant species. The main type of mutations of FNB mutants are deletions of DNA fragments ranging from few base pairs to several hundred kilobases, thus usually leading to the null mutation of genes. Despite its efficiency in mutagenesis, identification of the mutation sites is still challenging in many species. The traditional strategy of positional cloning is very effective in identifying the mutation but time-consuming. With the availability of genome sequences, the array-based comparative genomic hybridization (CGH) method has been developed to detect the mutation sites by comparing the signal intensities of probes between wild-type and mutant plants. Though CGH method is effective in detecting copy number variations (CNVs), the resolution and coverage of CGH probes are not adequate to identify mutations other than CNVs. RESULTS: We report a new strategy and pipeline to sensitively identify the mutation sites of FNB mutants by combining deep-coverage whole-genome sequencing (WGS), polymorphism calling, and customized filtering in Medicago truncatula. Initially, we performed a bulked sequencing for a FNB white nodule (wn) mutant and its wild-type like plants derived from a backcross population. Following polymorphism calling and filtering, validation by manual check and Sanger sequencing, we identified that SymCRK is the causative gene of white nodule mutant. We also sequenced an individual FNB mutant yellow leaves 1 (yl1) and wild-type plant. We identified that ETHYLENE-DEPENDENT GRAVITROPISM-DEFICIENT AND YELLOW-GREEN 1 (EGY1) is the candidate gene for M. truncatula yl1 mutant. CONCLUSION: Our results demonstrated that the method reported here is rather robust in identifying the mutation sites for FNB mutants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-021-00765-y. |
format | Online Article Text |
id | pubmed-8207604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82076042021-06-16 Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula Du, Huan Jiao, Zhicheng Liu, Junjie Huang, Wei Ge, Liangfa Plant Methods Methodology BACKGROUND: Fast neutron bombardment (FNB) is a very effective approach for mutagenesis and has been widely used in generating mutant libraries in many plant species. The main type of mutations of FNB mutants are deletions of DNA fragments ranging from few base pairs to several hundred kilobases, thus usually leading to the null mutation of genes. Despite its efficiency in mutagenesis, identification of the mutation sites is still challenging in many species. The traditional strategy of positional cloning is very effective in identifying the mutation but time-consuming. With the availability of genome sequences, the array-based comparative genomic hybridization (CGH) method has been developed to detect the mutation sites by comparing the signal intensities of probes between wild-type and mutant plants. Though CGH method is effective in detecting copy number variations (CNVs), the resolution and coverage of CGH probes are not adequate to identify mutations other than CNVs. RESULTS: We report a new strategy and pipeline to sensitively identify the mutation sites of FNB mutants by combining deep-coverage whole-genome sequencing (WGS), polymorphism calling, and customized filtering in Medicago truncatula. Initially, we performed a bulked sequencing for a FNB white nodule (wn) mutant and its wild-type like plants derived from a backcross population. Following polymorphism calling and filtering, validation by manual check and Sanger sequencing, we identified that SymCRK is the causative gene of white nodule mutant. We also sequenced an individual FNB mutant yellow leaves 1 (yl1) and wild-type plant. We identified that ETHYLENE-DEPENDENT GRAVITROPISM-DEFICIENT AND YELLOW-GREEN 1 (EGY1) is the candidate gene for M. truncatula yl1 mutant. CONCLUSION: Our results demonstrated that the method reported here is rather robust in identifying the mutation sites for FNB mutants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-021-00765-y. BioMed Central 2021-06-16 /pmc/articles/PMC8207604/ /pubmed/34134730 http://dx.doi.org/10.1186/s13007-021-00765-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Du, Huan Jiao, Zhicheng Liu, Junjie Huang, Wei Ge, Liangfa Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula |
title | Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula |
title_full | Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula |
title_fullStr | Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula |
title_full_unstemmed | Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula |
title_short | Rapid identification of mutations caused by fast neutron bombardment in Medicago truncatula |
title_sort | rapid identification of mutations caused by fast neutron bombardment in medicago truncatula |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207604/ https://www.ncbi.nlm.nih.gov/pubmed/34134730 http://dx.doi.org/10.1186/s13007-021-00765-y |
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