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Generation of peanut mutants by fast neutron irradiation combined with in vitro culture
Induced mutations have played an important role in the development of new plant varieties. In this study, we investigated the effects of fast neutron irradiation on somatic embryogenesis combined with plant regeneration in embryonic leaflet culture to develop new peanut (Arachis hypogaea L.) germpla...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426915/ https://www.ncbi.nlm.nih.gov/pubmed/25653418 http://dx.doi.org/10.1093/jrr/rru121 |
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author | Wang, Jing-Shan Sui, Jiong-Ming Xie, Yong-Dun Guo, Hui-Jun Qiao, Li-Xian Zhao, Li-Lan Yu, Shan-Lin Liu, Lu-Xiang |
author_facet | Wang, Jing-Shan Sui, Jiong-Ming Xie, Yong-Dun Guo, Hui-Jun Qiao, Li-Xian Zhao, Li-Lan Yu, Shan-Lin Liu, Lu-Xiang |
author_sort | Wang, Jing-Shan |
collection | PubMed |
description | Induced mutations have played an important role in the development of new plant varieties. In this study, we investigated the effects of fast neutron irradiation on somatic embryogenesis combined with plant regeneration in embryonic leaflet culture to develop new peanut (Arachis hypogaea L.) germplasm for breeding. The dry seeds of the elite cultivar Luhua 11 were irradiated with fast neutrons at dosages of 9.7, 14.0 and 18.0 Gy. The embryonic leaflets were separated and incubated in a medium with 10.0-mg/l 2,4-D to induce somatic embryogenesis. Next, they were incubated in a medium with 4.0-mg/l BAP for plant regeneration. As the irradiation dosage increased, the frequency of both somatic embryo formation and plantlet regeneration decreased. The regenerated plantlets were grafted onto rootstocks and were transplanted into the field. Later, the mature seeds of the regenerated plants were harvested. The M(2) generation plants from most of the regenerated cultivars exhibited variations and segregation in vigor, plant height, branch and pod number, pod size, and pod shape. To determine whether the phenotypes were associated with genomic modification, we compared the DNA polymorphisms between the wild-type plants and 19 M(3)-generation individuals from different regenerated plants. We used 20 pairs of simple sequence repeat (SSR) primers and detected polymorphisms between most of the mutants and the wild-type plants (Luhua 11). Our results indicate that using a combination of fast neutron irradiation and tissue culture is an effective approach for creating new peanut germplasm. |
format | Online Article Text |
id | pubmed-4426915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44269152015-05-15 Generation of peanut mutants by fast neutron irradiation combined with in vitro culture Wang, Jing-Shan Sui, Jiong-Ming Xie, Yong-Dun Guo, Hui-Jun Qiao, Li-Xian Zhao, Li-Lan Yu, Shan-Lin Liu, Lu-Xiang J Radiat Res Biology Induced mutations have played an important role in the development of new plant varieties. In this study, we investigated the effects of fast neutron irradiation on somatic embryogenesis combined with plant regeneration in embryonic leaflet culture to develop new peanut (Arachis hypogaea L.) germplasm for breeding. The dry seeds of the elite cultivar Luhua 11 were irradiated with fast neutrons at dosages of 9.7, 14.0 and 18.0 Gy. The embryonic leaflets were separated and incubated in a medium with 10.0-mg/l 2,4-D to induce somatic embryogenesis. Next, they were incubated in a medium with 4.0-mg/l BAP for plant regeneration. As the irradiation dosage increased, the frequency of both somatic embryo formation and plantlet regeneration decreased. The regenerated plantlets were grafted onto rootstocks and were transplanted into the field. Later, the mature seeds of the regenerated plants were harvested. The M(2) generation plants from most of the regenerated cultivars exhibited variations and segregation in vigor, plant height, branch and pod number, pod size, and pod shape. To determine whether the phenotypes were associated with genomic modification, we compared the DNA polymorphisms between the wild-type plants and 19 M(3)-generation individuals from different regenerated plants. We used 20 pairs of simple sequence repeat (SSR) primers and detected polymorphisms between most of the mutants and the wild-type plants (Luhua 11). Our results indicate that using a combination of fast neutron irradiation and tissue culture is an effective approach for creating new peanut germplasm. Oxford University Press 2015-05 2015-02-04 /pmc/articles/PMC4426915/ /pubmed/25653418 http://dx.doi.org/10.1093/jrr/rru121 Text en © The Author 2015. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biology Wang, Jing-Shan Sui, Jiong-Ming Xie, Yong-Dun Guo, Hui-Jun Qiao, Li-Xian Zhao, Li-Lan Yu, Shan-Lin Liu, Lu-Xiang Generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
title | Generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
title_full | Generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
title_fullStr | Generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
title_full_unstemmed | Generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
title_short | Generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
title_sort | generation of peanut mutants by fast neutron irradiation combined with in vitro culture |
topic | Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426915/ https://www.ncbi.nlm.nih.gov/pubmed/25653418 http://dx.doi.org/10.1093/jrr/rru121 |
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