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Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease
BACKGROUND: Morphogenic culture systems are central to crop improvement programs that utilize transgenic and genome editing technologies. We previously reported that CMD2-type cassava (Manihot esculenta) cultivars lose resistance to cassava mosaic disease (CMD) when passed through somatic embryogene...
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/PMC6020238/ https://www.ncbi.nlm.nih.gov/pubmed/29940871 http://dx.doi.org/10.1186/s12870-018-1354-x |
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author | Chauhan, Raj Deepika Beyene, Getu Taylor, Nigel J. |
author_facet | Chauhan, Raj Deepika Beyene, Getu Taylor, Nigel J. |
author_sort | Chauhan, Raj Deepika |
collection | PubMed |
description | BACKGROUND: Morphogenic culture systems are central to crop improvement programs that utilize transgenic and genome editing technologies. We previously reported that CMD2-type cassava (Manihot esculenta) cultivars lose resistance to cassava mosaic disease (CMD) when passed through somatic embryogenesis. As a result, these plants cannot be developed as products for deployment where CMD is endemic such as sub-Saharan Africa or the Indian sub-continent. RESULT: In order to increase understanding of this phenomenon, 21 African cassava cultivars were screened for resistance to CMD after regeneration through somatic embryogenesis. Fifteen cultivars were shown to retain resistance to CMD through somatic embryogenesis, confirming that the existing transformation and gene editing systems can be employed in these genetic backgrounds without compromising resistance to geminivirus infection. CMD2-type cultivars were also subjected to plant regeneration via caulogenesis and meristem tip culture, resulting in 25–36% and 5–10% of regenerated plant lines losing resistance to CMD respectively. CONCLUSIONS: This study provides clear evidence that multiple morphogenic systems can result in loss of resistance to CMD, and that somatic embryogenesis per se is not the underlying cause of this phenomenon. The information described here is critical for interpreting genomic, transcriptomic and epigenomic datasets aimed at understanding CMD resistance mechanisms in cassava. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1354-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6020238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60202382018-07-06 Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease Chauhan, Raj Deepika Beyene, Getu Taylor, Nigel J. BMC Plant Biol Research Article BACKGROUND: Morphogenic culture systems are central to crop improvement programs that utilize transgenic and genome editing technologies. We previously reported that CMD2-type cassava (Manihot esculenta) cultivars lose resistance to cassava mosaic disease (CMD) when passed through somatic embryogenesis. As a result, these plants cannot be developed as products for deployment where CMD is endemic such as sub-Saharan Africa or the Indian sub-continent. RESULT: In order to increase understanding of this phenomenon, 21 African cassava cultivars were screened for resistance to CMD after regeneration through somatic embryogenesis. Fifteen cultivars were shown to retain resistance to CMD through somatic embryogenesis, confirming that the existing transformation and gene editing systems can be employed in these genetic backgrounds without compromising resistance to geminivirus infection. CMD2-type cultivars were also subjected to plant regeneration via caulogenesis and meristem tip culture, resulting in 25–36% and 5–10% of regenerated plant lines losing resistance to CMD respectively. CONCLUSIONS: This study provides clear evidence that multiple morphogenic systems can result in loss of resistance to CMD, and that somatic embryogenesis per se is not the underlying cause of this phenomenon. The information described here is critical for interpreting genomic, transcriptomic and epigenomic datasets aimed at understanding CMD resistance mechanisms in cassava. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1354-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-25 /pmc/articles/PMC6020238/ /pubmed/29940871 http://dx.doi.org/10.1186/s12870-018-1354-x 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 Chauhan, Raj Deepika Beyene, Getu Taylor, Nigel J. Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
title | Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
title_full | Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
title_fullStr | Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
title_full_unstemmed | Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
title_short | Multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
title_sort | multiple morphogenic culture systems cause loss of resistance to cassava mosaic disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020238/ https://www.ncbi.nlm.nih.gov/pubmed/29940871 http://dx.doi.org/10.1186/s12870-018-1354-x |
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