Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis
Callogenesis, the process during which explants derived from differentiated plant tissues are subjected to a trans-differentiation step characterized by the proliferation of a mass of cells, is fundamental to indirect organogenesis and the establishment of cell suspension cultures. Therefore, unders...
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2021
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oai:doaj.org-article:05d39f4c3b2b40ec846b41c78bcc4b592021-11-25T17:55:23ZTranscriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis10.3390/ijms2222123191422-00671661-6596https://doaj.org/article/05d39f4c3b2b40ec846b41c78bcc4b592021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/22/12319https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Callogenesis, the process during which explants derived from differentiated plant tissues are subjected to a trans-differentiation step characterized by the proliferation of a mass of cells, is fundamental to indirect organogenesis and the establishment of cell suspension cultures. Therefore, understanding how callogenesis takes place is helpful to plant tissue culture, as well as to plant biotechnology and bioprocess engineering. The common herbaceous plant stinging nettle (<i>Urtica dioica</i> L.) is a species producing cellulosic fibres (the bast fibres) and a whole array of phytochemicals for pharmacological, nutraceutical and cosmeceutical use. Thus, it is of interest as a potential multi-purpose plant. In this study, callogenesis in internode explants of a nettle fibre clone (clone 13) was studied using RNA-Seq to understand which gene ontologies predominate at different time points. Callogenesis was induced with the plant growth regulators α-napthaleneacetic acid (NAA) and 6-benzyl aminopurine (BAP) after having determined their optimal concentrations. The process was studied over a period of 34 days, a time point at which a well-visible callus mass developed on the explants. The bioinformatic analysis of the transcriptomic dataset revealed specific gene ontologies characterizing each of the four time points investigated (0, 1, 10 and 34 days). The results show that, while the advanced stage of callogenesis is characterized by the iron deficiency response triggered by the high levels of reactive oxygen species accumulated by the proliferating cell mass, the intermediate and early phases are dominated by ontologies related to the immune response and cell wall loosening, respectively.Xuan XuSylvain LegayRoberto BerniJean-Francois HausmanGea GuerrieroMDPI AGarticlecallogenesistranscriptomicsstinging nettleqPCRplant growth regulatorsBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 12319, p 12319 (2021) |
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callogenesis transcriptomics stinging nettle qPCR plant growth regulators Biology (General) QH301-705.5 Chemistry QD1-999 |
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callogenesis transcriptomics stinging nettle qPCR plant growth regulators Biology (General) QH301-705.5 Chemistry QD1-999 Xuan Xu Sylvain Legay Roberto Berni Jean-Francois Hausman Gea Guerriero Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis |
description |
Callogenesis, the process during which explants derived from differentiated plant tissues are subjected to a trans-differentiation step characterized by the proliferation of a mass of cells, is fundamental to indirect organogenesis and the establishment of cell suspension cultures. Therefore, understanding how callogenesis takes place is helpful to plant tissue culture, as well as to plant biotechnology and bioprocess engineering. The common herbaceous plant stinging nettle (<i>Urtica dioica</i> L.) is a species producing cellulosic fibres (the bast fibres) and a whole array of phytochemicals for pharmacological, nutraceutical and cosmeceutical use. Thus, it is of interest as a potential multi-purpose plant. In this study, callogenesis in internode explants of a nettle fibre clone (clone 13) was studied using RNA-Seq to understand which gene ontologies predominate at different time points. Callogenesis was induced with the plant growth regulators α-napthaleneacetic acid (NAA) and 6-benzyl aminopurine (BAP) after having determined their optimal concentrations. The process was studied over a period of 34 days, a time point at which a well-visible callus mass developed on the explants. The bioinformatic analysis of the transcriptomic dataset revealed specific gene ontologies characterizing each of the four time points investigated (0, 1, 10 and 34 days). The results show that, while the advanced stage of callogenesis is characterized by the iron deficiency response triggered by the high levels of reactive oxygen species accumulated by the proliferating cell mass, the intermediate and early phases are dominated by ontologies related to the immune response and cell wall loosening, respectively. |
format |
article |
author |
Xuan Xu Sylvain Legay Roberto Berni Jean-Francois Hausman Gea Guerriero |
author_facet |
Xuan Xu Sylvain Legay Roberto Berni Jean-Francois Hausman Gea Guerriero |
author_sort |
Xuan Xu |
title |
Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis |
title_short |
Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis |
title_full |
Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis |
title_fullStr |
Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis |
title_full_unstemmed |
Transcriptomic Changes in Internode Explants of Stinging Nettle during Callogenesis |
title_sort |
transcriptomic changes in internode explants of stinging nettle during callogenesis |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/05d39f4c3b2b40ec846b41c78bcc4b59 |
work_keys_str_mv |
AT xuanxu transcriptomicchangesininternodeexplantsofstingingnettleduringcallogenesis AT sylvainlegay transcriptomicchangesininternodeexplantsofstingingnettleduringcallogenesis AT robertoberni transcriptomicchangesininternodeexplantsofstingingnettleduringcallogenesis AT jeanfrancoishausman transcriptomicchangesininternodeexplantsofstingingnettleduringcallogenesis AT geaguerriero transcriptomicchangesininternodeexplantsofstingingnettleduringcallogenesis |
_version_ |
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