MycorrhizaeV1, Main, Exploration, bibRecord, 000028

The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice.

Identifieur interne : 000028 ( Main/Exploration ); précédent : 000027; suivant : 000029

The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice.

Auteurs : Jeongmin Choi [Royaume-Uni] ; Tak Lee [Royaume-Uni] ; Jungnam Cho [Royaume-Uni, République populaire de Chine] ; Emily K. Servante [Royaume-Uni] ; Boas Pucker [Royaume-Uni, Allemagne] ; William Summers [Royaume-Uni] ; Sarah Bowden [Royaume-Uni] ; Mehran Rahimi [Pays-Bas] ; Kyungsook An [Corée du Sud] ; Gynheung An [Corée du Sud] ; Harro J. Bouwmeester [Pays-Bas] ; Emma J. Wallington [Royaume-Uni] ; Giles Oldroyd [Royaume-Uni] ; Uta Paszkowski [Royaume-Uni]

Source :

Nature communications [ 2041-1723 ] ; 2020.

RBID : pubmed:32355217

Descripteurs français

English descriptors

KwdEn :
- Arabidopsis (genetics), Arabidopsis (microbiology), Arabidopsis Proteins (genetics), Arabidopsis Proteins (physiology), Furans (metabolism), Gene Expression Regulation, Plant (MeSH), Germination (MeSH), Heterocyclic Compounds, 3-Ring (metabolism), Homozygote (MeSH), Intracellular Signaling Peptides and Proteins (genetics), Intracellular Signaling Peptides and Proteins (physiology), Lactones (metabolism), Multigene Family (MeSH), Mycorrhizae (physiology), Oryza (genetics), Oryza (microbiology), Phylogeny (MeSH), Plant Proteins (genetics), Plant Proteins (physiology), Plant Roots (microbiology), Pyrans (metabolism), RNA-Seq (MeSH), Signal Transduction (MeSH), Symbiosis (MeSH).
MESH :
- chemical , genetics : Arabidopsis Proteins, Intracellular Signaling Peptides and Proteins, Plant Proteins.
- genetics : Arabidopsis, Oryza.
- chemical , metabolism : Furans, Heterocyclic Compounds, 3-Ring, Lactones, Pyrans.
- microbiology : Arabidopsis, Oryza, Plant Roots.
- chemical , physiology : Arabidopsis Proteins, Intracellular Signaling Peptides and Proteins, Mycorrhizae, Plant Proteins.
- Gene Expression Regulation, Plant, Germination, Homozygote, Multigene Family, Phylogeny, RNA-Seq, Signal Transduction, Symbiosis.

Abstract

Most plants associate with beneficial arbuscular mycorrhizal (AM) fungi that facilitate soil nutrient acquisition. Prior to contact, partner recognition triggers reciprocal genetic remodelling to enable colonisation. The plant Dwarf14-Like (D14L) receptor conditions pre-symbiotic perception of AM fungi, and also detects the smoke constituent karrikin. D14L-dependent signalling mechanisms, underpinning AM symbiosis are unknown. Here, we present the identification of a negative regulator from rice, which operates downstream of the D14L receptor, corresponding to the homologue of the Arabidopsis thaliana Suppressor of MAX2-1 (AtSMAX1) that functions in karrikin signalling. We demonstrate that rice SMAX1 is a suppressor of AM symbiosis, negatively regulating fungal colonisation and transcription of crucial signalling components and conserved symbiosis genes. Similarly, rice SMAX1 negatively controls strigolactone biosynthesis, demonstrating an unexpected crosstalk between the strigolactone and karrikin signalling pathways. We conclude that removal of SMAX1, resulting from D14L signalling activation, de-represses essential symbiotic programmes and increases strigolactone hormone production.

DOI: 10.1038/s41467-020-16021-1
PubMed: 32355217
PubMed Central: PMC7193599

Affiliations:

Links toward previous steps (curation, corpus...)

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Le document en format XML

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<author><name sortKey="Wallington, Emma J" sort="Wallington, Emma J" uniqKey="Wallington E" first="Emma J" last="Wallington">Emma J. Wallington</name>
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<orgName type="university">Université de Cambridge</orgName>
<placeName><settlement type="city">Cambridge</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Angleterre de l'Est</region>
</placeName>
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<affiliation wicri:level="4"><nlm:affiliation>Sainsbury Laboratory, University of Cambridge, Bateman Street, Cambridge, CB2 1LR, UK.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
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<author><name sortKey="Paszkowski, Uta" sort="Paszkowski, Uta" uniqKey="Paszkowski U" first="Uta" last="Paszkowski">Uta Paszkowski</name>
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<series><title level="j">Nature communications</title>
<idno type="eISSN">2041-1723</idno>
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<term>Arabidopsis (microbiology)</term>
<term>Arabidopsis Proteins (genetics)</term>
<term>Arabidopsis Proteins (physiology)</term>
<term>Furans (metabolism)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Germination (MeSH)</term>
<term>Heterocyclic Compounds, 3-Ring (metabolism)</term>
<term>Homozygote (MeSH)</term>
<term>Intracellular Signaling Peptides and Proteins (genetics)</term>
<term>Intracellular Signaling Peptides and Proteins (physiology)</term>
<term>Lactones (metabolism)</term>
<term>Multigene Family (MeSH)</term>
<term>Mycorrhizae (physiology)</term>
<term>Oryza (genetics)</term>
<term>Oryza (microbiology)</term>
<term>Phylogeny (MeSH)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (physiology)</term>
<term>Plant Roots (microbiology)</term>
<term>Pyrans (metabolism)</term>
<term>RNA-Seq (MeSH)</term>
<term>Signal Transduction (MeSH)</term>
<term>Symbiosis (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Arabidopsis (génétique)</term>
<term>Arabidopsis (microbiologie)</term>
<term>Composés hétérocycliques 3 noyaux (métabolisme)</term>
<term>Famille multigénique (MeSH)</term>
<term>Furanes (métabolisme)</term>
<term>Germination (MeSH)</term>
<term>Homozygote (MeSH)</term>
<term>Lactones (métabolisme)</term>
<term>Mycorhizes (physiologie)</term>
<term>Oryza (génétique)</term>
<term>Oryza (microbiologie)</term>
<term>Phylogenèse (MeSH)</term>
<term>Protéines d'Arabidopsis (génétique)</term>
<term>Protéines d'Arabidopsis (physiologie)</term>
<term>Protéines et peptides de signalisation intracellulaire (génétique)</term>
<term>Protéines et peptides de signalisation intracellulaire (physiologie)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (physiologie)</term>
<term>Pyrannes (métabolisme)</term>
<term>Racines de plante (microbiologie)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Symbiose (MeSH)</term>
<term>Transduction du signal (MeSH)</term>
</keywords>
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<term>Intracellular Signaling Peptides and Proteins</term>
<term>Plant Proteins</term>
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<term>Protéines végétales</term>
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<term>Heterocyclic Compounds, 3-Ring</term>
<term>Lactones</term>
<term>Pyrans</term>
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<term>Oryza</term>
<term>Racines de plante</term>
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<term>Oryza</term>
<term>Plant Roots</term>
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<term>Furanes</term>
<term>Lactones</term>
<term>Pyrannes</term>
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<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Mycorhizes</term>
<term>Protéines d'Arabidopsis</term>
<term>Protéines et peptides de signalisation intracellulaire</term>
<term>Protéines végétales</term>
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<term>Intracellular Signaling Peptides and Proteins</term>
<term>Mycorrhizae</term>
<term>Plant Proteins</term>
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<keywords scheme="MESH" xml:lang="en"><term>Gene Expression Regulation, Plant</term>
<term>Germination</term>
<term>Homozygote</term>
<term>Multigene Family</term>
<term>Phylogeny</term>
<term>RNA-Seq</term>
<term>Signal Transduction</term>
<term>Symbiosis</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Famille multigénique</term>
<term>Germination</term>
<term>Homozygote</term>
<term>Phylogenèse</term>
<term>Régulation de l'expression des gènes végétaux</term>
<term>Symbiose</term>
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<front><div type="abstract" xml:lang="en">Most plants associate with beneficial arbuscular mycorrhizal (AM) fungi that facilitate soil nutrient acquisition. Prior to contact, partner recognition triggers reciprocal genetic remodelling to enable colonisation. The plant Dwarf14-Like (D14L) receptor conditions pre-symbiotic perception of AM fungi, and also detects the smoke constituent karrikin. D14L-dependent signalling mechanisms, underpinning AM symbiosis are unknown. Here, we present the identification of a negative regulator from rice, which operates downstream of the D14L receptor, corresponding to the homologue of the Arabidopsis thaliana Suppressor of MAX2-1 (AtSMAX1) that functions in karrikin signalling. We demonstrate that rice SMAX1 is a suppressor of AM symbiosis, negatively regulating fungal colonisation and transcription of crucial signalling components and conserved symbiosis genes. Similarly, rice SMAX1 negatively controls strigolactone biosynthesis, demonstrating an unexpected crosstalk between the strigolactone and karrikin signalling pathways. We conclude that removal of SMAX1, resulting from D14L signalling activation, de-represses essential symbiotic programmes and increases strigolactone hormone production.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">32355217</PMID>
<DateCompleted><Year>2020</Year>
<Month>08</Month>
<Day>07</Day>
</DateCompleted>
<DateRevised><Year>2020</Year>
<Month>08</Month>
<Day>07</Day>
</DateRevised>
<Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2041-1723</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>11</Volume>
<Issue>1</Issue>
<PubDate><Year>2020</Year>
<Month>04</Month>
<Day>30</Day>
</PubDate>
</JournalIssue>
<Title>Nature communications</Title>
<ISOAbbreviation>Nat Commun</ISOAbbreviation>
</Journal>
<ArticleTitle>The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice.</ArticleTitle>
<Pagination><MedlinePgn>2114</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1038/s41467-020-16021-1</ELocationID>
<Abstract><AbstractText>Most plants associate with beneficial arbuscular mycorrhizal (AM) fungi that facilitate soil nutrient acquisition. Prior to contact, partner recognition triggers reciprocal genetic remodelling to enable colonisation. The plant Dwarf14-Like (D14L) receptor conditions pre-symbiotic perception of AM fungi, and also detects the smoke constituent karrikin. D14L-dependent signalling mechanisms, underpinning AM symbiosis are unknown. Here, we present the identification of a negative regulator from rice, which operates downstream of the D14L receptor, corresponding to the homologue of the Arabidopsis thaliana Suppressor of MAX2-1 (AtSMAX1) that functions in karrikin signalling. We demonstrate that rice SMAX1 is a suppressor of AM symbiosis, negatively regulating fungal colonisation and transcription of crucial signalling components and conserved symbiosis genes. Similarly, rice SMAX1 negatively controls strigolactone biosynthesis, demonstrating an unexpected crosstalk between the strigolactone and karrikin signalling pathways. We conclude that removal of SMAX1, resulting from D14L signalling activation, de-represses essential symbiotic programmes and increases strigolactone hormone production.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Choi</LastName>
<ForeName>Jeongmin</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK. jc913@cam.ac.uk.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Lee</LastName>
<ForeName>Tak</ForeName>
<Initials>T</Initials>
<Identifier Source="ORCID">0000-0001-7008-7605</Identifier>
<AffiliationInfo><Affiliation>Sainsbury Laboratory, University of Cambridge, Bateman Street, Cambridge, CB2 1LR, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Cho</LastName>
<ForeName>Jungnam</ForeName>
<Initials>J</Initials>
<Identifier Source="ORCID">0000-0002-4078-7763</Identifier>
<AffiliationInfo><Affiliation>Sainsbury Laboratory, University of Cambridge, Bateman Street, Cambridge, CB2 1LR, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>CAS-JIC Centre of Excellence for Plant and Microbial Science, 200032, Shanghai, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Servante</LastName>
<ForeName>Emily K</ForeName>
<Initials>EK</Initials>
<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Pucker</LastName>
<ForeName>Boas</ForeName>
<Initials>B</Initials>
<Identifier Source="ORCID">0000-0002-3321-7471</Identifier>
<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Center for Biotechnology, Bielefeld University, Sequenz 1, 33615, Bielefeld, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Summers</LastName>
<ForeName>William</ForeName>
<Initials>W</Initials>
<Identifier Source="ORCID">0000-0002-4835-4743</Identifier>
<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bowden</LastName>
<ForeName>Sarah</ForeName>
<Initials>S</Initials>
<Identifier Source="ORCID">0000-0001-5105-076X</Identifier>
<AffiliationInfo><Affiliation>The John Bingham Laboratory, NIAB, Huntingdon Road, Cambridge, CB3 0LE, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Rahimi</LastName>
<ForeName>Mehran</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>An</LastName>
<ForeName>Kyungsook</ForeName>
<Initials>K</Initials>
<AffiliationInfo><Affiliation>Crop Biotech Institute, Kyung Hee University, Yongjin-si, 446-701, South Korea.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>An</LastName>
<ForeName>Gynheung</ForeName>
<Initials>G</Initials>
<AffiliationInfo><Affiliation>Crop Biotech Institute, Kyung Hee University, Yongjin-si, 446-701, South Korea.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bouwmeester</LastName>
<ForeName>Harro J</ForeName>
<Initials>HJ</Initials>
<Identifier Source="ORCID">0000-0003-0907-2732</Identifier>
<AffiliationInfo><Affiliation>Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wallington</LastName>
<ForeName>Emma J</ForeName>
<Initials>EJ</Initials>
<Identifier Source="ORCID">0000-0003-3715-7901</Identifier>
<AffiliationInfo><Affiliation>The John Bingham Laboratory, NIAB, Huntingdon Road, Cambridge, CB3 0LE, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Oldroyd</LastName>
<ForeName>Giles</ForeName>
<Initials>G</Initials>
<Identifier Source="ORCID">0000-0002-5245-6355</Identifier>
<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Sainsbury Laboratory, University of Cambridge, Bateman Street, Cambridge, CB2 1LR, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Paszkowski</LastName>
<ForeName>Uta</ForeName>
<Initials>U</Initials>
<Identifier Source="ORCID">0000-0002-7279-7632</Identifier>
<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK. up220@cam.ac.uk.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>BB/P003419/1</GrantID>
<Acronym>BB_</Acronym>
<Agency>Biotechnology and Biological Sciences Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><GrantID>BB/P003176/1</GrantID>
<Acronym>BB_</Acronym>
<Agency>Biotechnology and Biological Sciences Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2020</Year>
<Month>04</Month>
<Day>30</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Nat Commun</MedlineTA>
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<ISSNLinking>2041-1723</ISSNLinking>
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<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
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<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
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<MeshHeading><DescriptorName UI="D018525" MajorTopicYN="N">Germination</DescriptorName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
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<MeshHeading><DescriptorName UI="D012275" MajorTopicYN="N">Oryza</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011714" MajorTopicYN="N">Pyrans</DescriptorName>
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<MeshHeading><DescriptorName UI="D000081246" MajorTopicYN="N">RNA-Seq</DescriptorName>
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The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice.

The negative regulator SMAX1 controls mycorrhizal symbiosis and strigolactone biosynthesis in rice.

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