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Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation

Agrobacterium tumefaciens infection of wounded plant tissues causes the formation of crown gall tumors. Upon infection, genes encoded on the A. tumefaciens tumor inducing plasmid are integrated in the plant genome to induce the biosynthesis of auxin and cytokinin, leading to uncontrolled cell divisi...

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Autores principales: Kerpen, Lucy, Niccolini, Luca, Licausi, Francesco, van Dongen, Joost T., Weits, Daan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371838/
https://www.ncbi.nlm.nih.gov/pubmed/30804956
http://dx.doi.org/10.3389/fpls.2019.00056
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author Kerpen, Lucy
Niccolini, Luca
Licausi, Francesco
van Dongen, Joost T.
Weits, Daan A.
author_facet Kerpen, Lucy
Niccolini, Luca
Licausi, Francesco
van Dongen, Joost T.
Weits, Daan A.
author_sort Kerpen, Lucy
collection PubMed
description Agrobacterium tumefaciens infection of wounded plant tissues causes the formation of crown gall tumors. Upon infection, genes encoded on the A. tumefaciens tumor inducing plasmid are integrated in the plant genome to induce the biosynthesis of auxin and cytokinin, leading to uncontrolled cell division. Additional sequences present on the bacterial T-DNA encode for opine biosynthesis genes, which induce the production of opines that act as a unique carbon and nitrogen source for Agrobacterium. Crown galls therefore become a very strong sink for photosynthate. Here we found that the increased metabolic demand in crown galls causes an increase in oxygen consumption rate, which leads to a steep drop in the internal oxygen concentration. Consistent with this, plant hypoxia-responsive genes were found to be significantly upregulated in crown galls compared to uninfected stem tissue. Following this observation, we aimed at understanding whether the low-oxygen response pathway, mediated by group VII ethylene response factor (ERF-VII) transcription factors, plays a role in the development of crown galls. We found that quintuple knock-out mutants of all ERF-VII members, which are incapable of inducing the hypoxic response, show reduced crown gall symptoms. Conversely, mutant genotypes characterized by constitutively high levels of hypoxia-associated transcripts, displayed more severe crown gall symptoms. Based on these results, we concluded that uncontrolled cell proliferation of crown galls established hypoxic conditions, thereby requiring adequate anaerobic responses of the plant tissue to support tumor growth.
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spelling pubmed-63718382019-02-25 Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation Kerpen, Lucy Niccolini, Luca Licausi, Francesco van Dongen, Joost T. Weits, Daan A. Front Plant Sci Plant Science Agrobacterium tumefaciens infection of wounded plant tissues causes the formation of crown gall tumors. Upon infection, genes encoded on the A. tumefaciens tumor inducing plasmid are integrated in the plant genome to induce the biosynthesis of auxin and cytokinin, leading to uncontrolled cell division. Additional sequences present on the bacterial T-DNA encode for opine biosynthesis genes, which induce the production of opines that act as a unique carbon and nitrogen source for Agrobacterium. Crown galls therefore become a very strong sink for photosynthate. Here we found that the increased metabolic demand in crown galls causes an increase in oxygen consumption rate, which leads to a steep drop in the internal oxygen concentration. Consistent with this, plant hypoxia-responsive genes were found to be significantly upregulated in crown galls compared to uninfected stem tissue. Following this observation, we aimed at understanding whether the low-oxygen response pathway, mediated by group VII ethylene response factor (ERF-VII) transcription factors, plays a role in the development of crown galls. We found that quintuple knock-out mutants of all ERF-VII members, which are incapable of inducing the hypoxic response, show reduced crown gall symptoms. Conversely, mutant genotypes characterized by constitutively high levels of hypoxia-associated transcripts, displayed more severe crown gall symptoms. Based on these results, we concluded that uncontrolled cell proliferation of crown galls established hypoxic conditions, thereby requiring adequate anaerobic responses of the plant tissue to support tumor growth. Frontiers Media S.A. 2019-02-05 /pmc/articles/PMC6371838/ /pubmed/30804956 http://dx.doi.org/10.3389/fpls.2019.00056 Text en Copyright © 2019 Kerpen, Niccolini, Licausi, van Dongen and Weits. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Kerpen, Lucy
Niccolini, Luca
Licausi, Francesco
van Dongen, Joost T.
Weits, Daan A.
Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation
title Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation
title_full Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation
title_fullStr Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation
title_full_unstemmed Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation
title_short Hypoxic Conditions in Crown Galls Induce Plant Anaerobic Responses That Support Tumor Proliferation
title_sort hypoxic conditions in crown galls induce plant anaerobic responses that support tumor proliferation
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371838/
https://www.ncbi.nlm.nih.gov/pubmed/30804956
http://dx.doi.org/10.3389/fpls.2019.00056
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