Differentiation of symbiotic cells and endosymbionts in Medicago truncatula nodulation are coupled to two transcriptome-switches
The legume plant Medicago truncatula establishes a symbiosis with the nitrogen-fixing bacterium Sinorhizobium meliloti which takes place in root nodules. The formation of nodules employs a complex developmental program involving organogenesis, specific cellular differentiation of the host cells and...
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creator | Maunoury, Nicolas Redondo-Nieto, Miguel Bourcy, Marie Van de Velde, Willem Alunni, Benoit Laporte, Philippe Durand, Patricia Agier, Nicolas Marisa, Laetitia Vaubert, Danièle Delacroix, Hervé Duc, Gérard Ratet, Pascal Aggerbeck, Lawrence Kondorosi, Eva Mergaert, Peter |
description | The legume plant Medicago truncatula establishes a symbiosis with the nitrogen-fixing bacterium Sinorhizobium meliloti which takes place in root nodules. The formation of nodules employs a complex developmental program involving organogenesis, specific cellular differentiation of the host cells and the endosymbiotic bacteria, called bacteroids, as well as the specific activation of a large number of plant genes. By using a collection of plant and bacterial mutants inducing non-functional, Fix(-) nodules, we studied the differentiation processes of the symbiotic partners together with the nodule transcriptome, with the aim of unravelling links between cell differentiation and transcriptome activation. Two waves of transcriptional reprogramming involving the repression and the massive induction of hundreds of genes were observed during wild-type nodule formation. The dominant features of this "nodule-specific transcriptome" were the repression of plant defense-related genes, the transient activation of cell cycle and protein synthesis genes at the early stage of nodule development and the activation of the secretory pathway along with a large number of transmembrane and secretory proteins or peptides throughout organogenesis. The fifteen plant and bacterial mutants that were analyzed fell into four major categories. Members of the first category of mutants formed non-functional nodules although they had differentiated nodule cells and bacteroids. This group passed the two transcriptome switch-points similarly to the wild type. The second category, which formed nodules in which the plant cells were differentiated and infected but the bacteroids did not differentiate, passed the first transcriptome switch but not the second one. Nodules in the third category contained infection threads but were devoid of differentiated symbiotic cells and displayed a root-like transcriptome. Nodules in the fourth category were free of bacteria, devoid of differentiated symbiotic cells and also displayed a root-like transcriptome. A correlation thus exists between the differentiation of symbiotic nodule cells and the first wave of nodule specific gene activation and between differentiation of rhizobia to bacteroids and the second transcriptome wave in nodules. The differentiation of symbiotic cells and of bacteroids may therefore constitute signals for the execution of these transcriptome-switches. |
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The formation of nodules employs a complex developmental program involving organogenesis, specific cellular differentiation of the host cells and the endosymbiotic bacteria, called bacteroids, as well as the specific activation of a large number of plant genes. By using a collection of plant and bacterial mutants inducing non-functional, Fix(-) nodules, we studied the differentiation processes of the symbiotic partners together with the nodule transcriptome, with the aim of unravelling links between cell differentiation and transcriptome activation. Two waves of transcriptional reprogramming involving the repression and the massive induction of hundreds of genes were observed during wild-type nodule formation. The dominant features of this "nodule-specific transcriptome" were the repression of plant defense-related genes, the transient activation of cell cycle and protein synthesis genes at the early stage of nodule development and the activation of the secretory pathway along with a large number of transmembrane and secretory proteins or peptides throughout organogenesis. The fifteen plant and bacterial mutants that were analyzed fell into four major categories. Members of the first category of mutants formed non-functional nodules although they had differentiated nodule cells and bacteroids. This group passed the two transcriptome switch-points similarly to the wild type. The second category, which formed nodules in which the plant cells were differentiated and infected but the bacteroids did not differentiate, passed the first transcriptome switch but not the second one. Nodules in the third category contained infection threads but were devoid of differentiated symbiotic cells and displayed a root-like transcriptome. Nodules in the fourth category were free of bacteria, devoid of differentiated symbiotic cells and also displayed a root-like transcriptome. A correlation thus exists between the differentiation of symbiotic nodule cells and the first wave of nodule specific gene activation and between differentiation of rhizobia to bacteroids and the second transcriptome wave in nodules. The differentiation of symbiotic cells and of bacteroids may therefore constitute signals for the execution of these transcriptome-switches.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0009519</identifier><identifier>PMID: 20209049</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>21st century ; Alfalfa ; Algorithms ; Arabidopsis ; Bacteria ; Bacteroids ; Cell activation ; Cell cycle ; Cell Differentiation ; Cell division ; Cellular Biology ; Deoxyribonucleic acid ; Developmental biology ; Developmental stages ; Differentiation (biology) ; DNA ; Endosymbionts ; Evolution ; Expressed Sequence Tags ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Bacterial ; Gene Expression Regulation, Plant ; Gene silencing ; Genes ; Genetic Markers ; Genetics and Genomics/Plant Genetics and Gene Expression ; Genomes ; Infections ; Legumes ; Life Sciences ; Mathematical models ; Medicago - metabolism ; Medicago truncatula ; Mutagenesis ; Mutants ; Mutation ; Nitrogen ; Nitrogen - chemistry ; Nitrogen Fixation ; Nodulation ; Nodules ; Organogenesis ; Peptides ; Phenotype ; Plant Biology/Plant Cell Biology ; Plant Biology/Plant-Biotic Interactions ; Plant cells ; Plant genetics ; Ploidies ; Protein biosynthesis ; Protein synthesis ; Proteins ; Root nodules ; Senescence ; Sinorhizobium meliloti - genetics ; Switches ; Symbiosis ; Symbiosis - physiology ; Transcription (Genetics) ; Transcription activation</subject><ispartof>PloS one, 2010-03, Vol.5 (3), p.e9519-e9519</ispartof><rights>COPYRIGHT 2010 Public Library of Science</rights><rights>2010 Maunoury et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Maunoury et al. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c791t-d60df588a219886ba3130397e4333a3bba3f781d68fd441e658359cef390f5a63</citedby><orcidid>0000-0002-8621-1495 ; 0000-0002-4065-8515 ; 0000-0002-5919-7317</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832008/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832008/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20209049$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02661146$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Bendahmane, Mohammed</contributor><creatorcontrib>Maunoury, Nicolas</creatorcontrib><creatorcontrib>Redondo-Nieto, Miguel</creatorcontrib><creatorcontrib>Bourcy, Marie</creatorcontrib><creatorcontrib>Van de Velde, Willem</creatorcontrib><creatorcontrib>Alunni, Benoit</creatorcontrib><creatorcontrib>Laporte, Philippe</creatorcontrib><creatorcontrib>Durand, Patricia</creatorcontrib><creatorcontrib>Agier, Nicolas</creatorcontrib><creatorcontrib>Marisa, Laetitia</creatorcontrib><creatorcontrib>Vaubert, Danièle</creatorcontrib><creatorcontrib>Delacroix, Hervé</creatorcontrib><creatorcontrib>Duc, Gérard</creatorcontrib><creatorcontrib>Ratet, Pascal</creatorcontrib><creatorcontrib>Aggerbeck, Lawrence</creatorcontrib><creatorcontrib>Kondorosi, Eva</creatorcontrib><creatorcontrib>Mergaert, Peter</creatorcontrib><title>Differentiation of symbiotic cells and endosymbionts in Medicago truncatula nodulation are coupled to two transcriptome-switches</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The legume plant Medicago truncatula establishes a symbiosis with the nitrogen-fixing bacterium Sinorhizobium meliloti which takes place in root nodules. The formation of nodules employs a complex developmental program involving organogenesis, specific cellular differentiation of the host cells and the endosymbiotic bacteria, called bacteroids, as well as the specific activation of a large number of plant genes. By using a collection of plant and bacterial mutants inducing non-functional, Fix(-) nodules, we studied the differentiation processes of the symbiotic partners together with the nodule transcriptome, with the aim of unravelling links between cell differentiation and transcriptome activation. Two waves of transcriptional reprogramming involving the repression and the massive induction of hundreds of genes were observed during wild-type nodule formation. The dominant features of this "nodule-specific transcriptome" were the repression of plant defense-related genes, the transient activation of cell cycle and protein synthesis genes at the early stage of nodule development and the activation of the secretory pathway along with a large number of transmembrane and secretory proteins or peptides throughout organogenesis. The fifteen plant and bacterial mutants that were analyzed fell into four major categories. Members of the first category of mutants formed non-functional nodules although they had differentiated nodule cells and bacteroids. This group passed the two transcriptome switch-points similarly to the wild type. The second category, which formed nodules in which the plant cells were differentiated and infected but the bacteroids did not differentiate, passed the first transcriptome switch but not the second one. Nodules in the third category contained infection threads but were devoid of differentiated symbiotic cells and displayed a root-like transcriptome. Nodules in the fourth category were free of bacteria, devoid of differentiated symbiotic cells and also displayed a root-like transcriptome. A correlation thus exists between the differentiation of symbiotic nodule cells and the first wave of nodule specific gene activation and between differentiation of rhizobia to bacteroids and the second transcriptome wave in nodules. The differentiation of symbiotic cells and of bacteroids may therefore constitute signals for the execution of these transcriptome-switches.</description><subject>21st century</subject><subject>Alfalfa</subject><subject>Algorithms</subject><subject>Arabidopsis</subject><subject>Bacteria</subject><subject>Bacteroids</subject><subject>Cell activation</subject><subject>Cell cycle</subject><subject>Cell Differentiation</subject><subject>Cell division</subject><subject>Cellular Biology</subject><subject>Deoxyribonucleic acid</subject><subject>Developmental biology</subject><subject>Developmental stages</subject><subject>Differentiation (biology)</subject><subject>DNA</subject><subject>Endosymbionts</subject><subject>Evolution</subject><subject>Expressed Sequence Tags</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Gene Expression Regulation, Plant</subject><subject>Gene silencing</subject><subject>Genes</subject><subject>Genetic Markers</subject><subject>Genetics and Genomics/Plant Genetics and Gene Expression</subject><subject>Genomes</subject><subject>Infections</subject><subject>Legumes</subject><subject>Life Sciences</subject><subject>Mathematical models</subject><subject>Medicago - metabolism</subject><subject>Medicago truncatula</subject><subject>Mutagenesis</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Nitrogen</subject><subject>Nitrogen - chemistry</subject><subject>Nitrogen Fixation</subject><subject>Nodulation</subject><subject>Nodules</subject><subject>Organogenesis</subject><subject>Peptides</subject><subject>Phenotype</subject><subject>Plant Biology/Plant Cell Biology</subject><subject>Plant Biology/Plant-Biotic Interactions</subject><subject>Plant cells</subject><subject>Plant genetics</subject><subject>Ploidies</subject><subject>Protein biosynthesis</subject><subject>Protein synthesis</subject><subject>Proteins</subject><subject>Root nodules</subject><subject>Senescence</subject><subject>Sinorhizobium meliloti - genetics</subject><subject>Switches</subject><subject>Symbiosis</subject><subject>Symbiosis - physiology</subject><subject>Transcription (Genetics)</subject><subject>Transcription 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Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maunoury, Nicolas</au><au>Redondo-Nieto, Miguel</au><au>Bourcy, Marie</au><au>Van de Velde, Willem</au><au>Alunni, Benoit</au><au>Laporte, Philippe</au><au>Durand, Patricia</au><au>Agier, Nicolas</au><au>Marisa, Laetitia</au><au>Vaubert, Danièle</au><au>Delacroix, Hervé</au><au>Duc, Gérard</au><au>Ratet, Pascal</au><au>Aggerbeck, Lawrence</au><au>Kondorosi, Eva</au><au>Mergaert, Peter</au><au>Bendahmane, Mohammed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differentiation of symbiotic cells and endosymbionts in Medicago truncatula nodulation are coupled to two transcriptome-switches</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2010-03-04</date><risdate>2010</risdate><volume>5</volume><issue>3</issue><spage>e9519</spage><epage>e9519</epage><pages>e9519-e9519</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The legume plant Medicago truncatula establishes a symbiosis with the nitrogen-fixing bacterium Sinorhizobium meliloti which takes place in root nodules. The formation of nodules employs a complex developmental program involving organogenesis, specific cellular differentiation of the host cells and the endosymbiotic bacteria, called bacteroids, as well as the specific activation of a large number of plant genes. By using a collection of plant and bacterial mutants inducing non-functional, Fix(-) nodules, we studied the differentiation processes of the symbiotic partners together with the nodule transcriptome, with the aim of unravelling links between cell differentiation and transcriptome activation. Two waves of transcriptional reprogramming involving the repression and the massive induction of hundreds of genes were observed during wild-type nodule formation. The dominant features of this "nodule-specific transcriptome" were the repression of plant defense-related genes, the transient activation of cell cycle and protein synthesis genes at the early stage of nodule development and the activation of the secretory pathway along with a large number of transmembrane and secretory proteins or peptides throughout organogenesis. The fifteen plant and bacterial mutants that were analyzed fell into four major categories. Members of the first category of mutants formed non-functional nodules although they had differentiated nodule cells and bacteroids. This group passed the two transcriptome switch-points similarly to the wild type. The second category, which formed nodules in which the plant cells were differentiated and infected but the bacteroids did not differentiate, passed the first transcriptome switch but not the second one. Nodules in the third category contained infection threads but were devoid of differentiated symbiotic cells and displayed a root-like transcriptome. Nodules in the fourth category were free of bacteria, devoid of differentiated symbiotic cells and also displayed a root-like transcriptome. A correlation thus exists between the differentiation of symbiotic nodule cells and the first wave of nodule specific gene activation and between differentiation of rhizobia to bacteroids and the second transcriptome wave in nodules. The differentiation of symbiotic cells and of bacteroids may therefore constitute signals for the execution of these transcriptome-switches.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>20209049</pmid><doi>10.1371/journal.pone.0009519</doi><tpages>e9519</tpages><orcidid>https://orcid.org/0000-0002-8621-1495</orcidid><orcidid>https://orcid.org/0000-0002-4065-8515</orcidid><orcidid>https://orcid.org/0000-0002-5919-7317</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2010-03, Vol.5 (3), p.e9519-e9519 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1289429844 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | 21st century Alfalfa Algorithms Arabidopsis Bacteria Bacteroids Cell activation Cell cycle Cell Differentiation Cell division Cellular Biology Deoxyribonucleic acid Developmental biology Developmental stages Differentiation (biology) DNA Endosymbionts Evolution Expressed Sequence Tags Gene expression Gene Expression Profiling Gene Expression Regulation, Bacterial Gene Expression Regulation, Plant Gene silencing Genes Genetic Markers Genetics and Genomics/Plant Genetics and Gene Expression Genomes Infections Legumes Life Sciences Mathematical models Medicago - metabolism Medicago truncatula Mutagenesis Mutants Mutation Nitrogen Nitrogen - chemistry Nitrogen Fixation Nodulation Nodules Organogenesis Peptides Phenotype Plant Biology/Plant Cell Biology Plant Biology/Plant-Biotic Interactions Plant cells Plant genetics Ploidies Protein biosynthesis Protein synthesis Proteins Root nodules Senescence Sinorhizobium meliloti - genetics Switches Symbiosis Symbiosis - physiology Transcription (Genetics) Transcription activation |
title | Differentiation of symbiotic cells and endosymbionts in Medicago truncatula nodulation are coupled to two transcriptome-switches |
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