Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis

Five ethylene-insensitive loci (wei1-wei5) were identified by using a low-dose screen for "weak" ethylene-insensitive mutants. wei1, wei2, and wei3 seedlings showed hormone insensitivity only in roots, whereas wei4 and wei5 displayed insensitivity in both roots and hypocotyls. The genes co...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2003-03, Vol.100 (5), p.2992-2997
Hauptverfasser: Alonso, J.M, Stepanova, A.N, Solano, R, Wisman, E, Ferrari, S, Ausubel, F.M, Ecker, J.R
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2997
container_issue 5
container_start_page 2992
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 100
creator Alonso, J.M
Stepanova, A.N
Solano, R
Wisman, E
Ferrari, S
Ausubel, F.M
Ecker, J.R
description Five ethylene-insensitive loci (wei1-wei5) were identified by using a low-dose screen for "weak" ethylene-insensitive mutants. wei1, wei2, and wei3 seedlings showed hormone insensitivity only in roots, whereas wei4 and wei5 displayed insensitivity in both roots and hypocotyls. The genes corresponding to wei1, wei4, and wei5 were isolated using a positional cloning approach. The wei1 mutant harbored a recessive mutation in TIR1, which encodes a component of the SCF protein ubiquitin ligase involved in the auxin response, wei4, a dominant mutant, resulted from a mutation in the ethylene receptor ERS, whereas wei5, a semidominant mutant, was caused by a mutation in the EIN3-related transcription factor gene EIL1. The simultaneous loss of functional WEI5/EIL1 and EIN3 nearly completely abolished the ethylene response in etiolated seedlings, and adult plants were highly susceptible to infection by the necrotrophic fungal pathogen Botrytis cinerea. Moreover, wei5/eil1 ein3 double mutants were able to fully suppress constitutive signaling caused by ctr1, suggesting a synergistic interaction among these gene products. Unlike previously known root ethylene-insensitive mutants, wei2 and wei3 were not affected in their response to auxin and showed a normal response to gravity. Genetic mapping studies indicate that wei2 and wei3 correspond to previously unidentified ethylene pathway genes that may control cell-elongation processes functioning at the intersection of the ethylene and auxin response pathways.
doi_str_mv 10.1073/pnas.0438070100
format Article
fullrecord <record><control><sourceid>jstor_fao_a</sourceid><recordid>TN_cdi_fao_agris_US201301068006</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>3139641</jstor_id><sourcerecordid>3139641</sourcerecordid><originalsourceid>FETCH-LOGICAL-c546t-588ea4f9ca94788823f11c11cab4846f547633cb2b217235ffa5dbbc4aa9e4963</originalsourceid><addsrcrecordid>eNptkc1v1DAQxSMEokvhzAWBxQFOaccfcewDh6qigFSJA_RsOYnd9ZLEwXZaVuofX0e76haEZGkO7_eeZ_SK4jWGEww1PZ1GHU-AUQE1YIAnxQqDxCVnEp4WKwBSl4IRdlS8iHEDALIS8Lw4woQDr0m9Ku4u3I1BrR8mP5oxReQtSmuDTFpvezOaMpiYpWjQpNP6Vm-R6zLnrDMdciPSKLbBmBFZH9Ct0b8OTpddY3Rp-WCYk17Ss-Ms6MZ1foouviyeWd1H82o_j4uri88_z7-Wl9-_fDs_uyzbivFUVkIYzaxstWS1EIJQi3Gbn26YYNxWrOaUtg1pCK4JrazVVdc0LdNaGiY5PS4-7XKnuRlM1-YDgu7VFNygw1Z57dTfyujW6trfKFxhVrHs_7D3B_97NjGpwcXW9L0ejZ-jwoILJjBk8P0_4MbPYcy3KQKYUkmoyNDpDmqDjzEY-7AIBrW0qpZW1aHV7Hj7eP8Dv68xAx_3wOI8xIGqFJGSKDv3fTJ_0qOo_5MZeLMDNjH58EBQTCVnOMvvdrLVXunr4KK6-rHclhflAoDTe7usy2U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201339238</pqid></control><display><type>article</type><title>Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis</title><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Alonso, J.M ; Stepanova, A.N ; Solano, R ; Wisman, E ; Ferrari, S ; Ausubel, F.M ; Ecker, J.R</creator><creatorcontrib>Alonso, J.M ; Stepanova, A.N ; Solano, R ; Wisman, E ; Ferrari, S ; Ausubel, F.M ; Ecker, J.R</creatorcontrib><description>Five ethylene-insensitive loci (wei1-wei5) were identified by using a low-dose screen for "weak" ethylene-insensitive mutants. wei1, wei2, and wei3 seedlings showed hormone insensitivity only in roots, whereas wei4 and wei5 displayed insensitivity in both roots and hypocotyls. The genes corresponding to wei1, wei4, and wei5 were isolated using a positional cloning approach. The wei1 mutant harbored a recessive mutation in TIR1, which encodes a component of the SCF protein ubiquitin ligase involved in the auxin response, wei4, a dominant mutant, resulted from a mutation in the ethylene receptor ERS, whereas wei5, a semidominant mutant, was caused by a mutation in the EIN3-related transcription factor gene EIL1. The simultaneous loss of functional WEI5/EIL1 and EIN3 nearly completely abolished the ethylene response in etiolated seedlings, and adult plants were highly susceptible to infection by the necrotrophic fungal pathogen Botrytis cinerea. Moreover, wei5/eil1 ein3 double mutants were able to fully suppress constitutive signaling caused by ctr1, suggesting a synergistic interaction among these gene products. Unlike previously known root ethylene-insensitive mutants, wei2 and wei3 were not affected in their response to auxin and showed a normal response to gravity. Genetic mapping studies indicate that wei2 and wei3 correspond to previously unidentified ethylene pathway genes that may control cell-elongation processes functioning at the intersection of the ethylene and auxin response pathways.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0438070100</identifier><identifier>PMID: 12606727</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>1-aminocyclopropane-1-carboxylic acid ; 2,4-D ; Alleles ; Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis thaliana ; Auxins ; Biological Sciences ; Botrytis - growth &amp; development ; Botrytis - pathogenicity ; Botrytis cinerea ; ethylene ; ethylene receptors ; Ethylenes - pharmacology ; fungal diseases of plants ; Gene Expression Regulation, Plant - drug effects ; genes ; Genes, Dominant ; Genetic Complementation Test ; Genetic mutation ; Genetic Techniques ; Genotype ; Hormones ; Hypocotyls ; ligases ; loci ; Mitosporic Fungi - growth &amp; development ; Mitosporic Fungi - pathogenicity ; Models, Genetic ; Mutagenesis, Site-Directed ; mutants ; Mutation ; Neurotransmitters ; pathogenesis ; Phenotypes ; Plant Diseases - genetics ; Plant Diseases - microbiology ; Plant Growth Regulators - pharmacology ; plant pathogenic fungi ; Plant roots ; Plants ; Polymerase Chain Reaction ; Receptors ; root growth ; seedling growth ; Seedlings ; Signal Transduction ; transcription factors ; ubiquitin ligase ; wei genes</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2003-03, Vol.100 (5), p.2992-2997</ispartof><rights>Copyright 1993-2003 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Mar 4, 2003</rights><rights>Copyright © 2003, The National Academy of Sciences 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c546t-588ea4f9ca94788823f11c11cab4846f547633cb2b217235ffa5dbbc4aa9e4963</citedby><cites>FETCH-LOGICAL-c546t-588ea4f9ca94788823f11c11cab4846f547633cb2b217235ffa5dbbc4aa9e4963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/100/5.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3139641$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3139641$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12606727$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alonso, J.M</creatorcontrib><creatorcontrib>Stepanova, A.N</creatorcontrib><creatorcontrib>Solano, R</creatorcontrib><creatorcontrib>Wisman, E</creatorcontrib><creatorcontrib>Ferrari, S</creatorcontrib><creatorcontrib>Ausubel, F.M</creatorcontrib><creatorcontrib>Ecker, J.R</creatorcontrib><title>Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Five ethylene-insensitive loci (wei1-wei5) were identified by using a low-dose screen for "weak" ethylene-insensitive mutants. wei1, wei2, and wei3 seedlings showed hormone insensitivity only in roots, whereas wei4 and wei5 displayed insensitivity in both roots and hypocotyls. The genes corresponding to wei1, wei4, and wei5 were isolated using a positional cloning approach. The wei1 mutant harbored a recessive mutation in TIR1, which encodes a component of the SCF protein ubiquitin ligase involved in the auxin response, wei4, a dominant mutant, resulted from a mutation in the ethylene receptor ERS, whereas wei5, a semidominant mutant, was caused by a mutation in the EIN3-related transcription factor gene EIL1. The simultaneous loss of functional WEI5/EIL1 and EIN3 nearly completely abolished the ethylene response in etiolated seedlings, and adult plants were highly susceptible to infection by the necrotrophic fungal pathogen Botrytis cinerea. Moreover, wei5/eil1 ein3 double mutants were able to fully suppress constitutive signaling caused by ctr1, suggesting a synergistic interaction among these gene products. Unlike previously known root ethylene-insensitive mutants, wei2 and wei3 were not affected in their response to auxin and showed a normal response to gravity. Genetic mapping studies indicate that wei2 and wei3 correspond to previously unidentified ethylene pathway genes that may control cell-elongation processes functioning at the intersection of the ethylene and auxin response pathways.</description><subject>1-aminocyclopropane-1-carboxylic acid</subject><subject>2,4-D</subject><subject>Alleles</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Auxins</subject><subject>Biological Sciences</subject><subject>Botrytis - growth &amp; development</subject><subject>Botrytis - pathogenicity</subject><subject>Botrytis cinerea</subject><subject>ethylene</subject><subject>ethylene receptors</subject><subject>Ethylenes - pharmacology</subject><subject>fungal diseases of plants</subject><subject>Gene Expression Regulation, Plant - drug effects</subject><subject>genes</subject><subject>Genes, Dominant</subject><subject>Genetic Complementation Test</subject><subject>Genetic mutation</subject><subject>Genetic Techniques</subject><subject>Genotype</subject><subject>Hormones</subject><subject>Hypocotyls</subject><subject>ligases</subject><subject>loci</subject><subject>Mitosporic Fungi - growth &amp; development</subject><subject>Mitosporic Fungi - pathogenicity</subject><subject>Models, Genetic</subject><subject>Mutagenesis, Site-Directed</subject><subject>mutants</subject><subject>Mutation</subject><subject>Neurotransmitters</subject><subject>pathogenesis</subject><subject>Phenotypes</subject><subject>Plant Diseases - genetics</subject><subject>Plant Diseases - microbiology</subject><subject>Plant Growth Regulators - pharmacology</subject><subject>plant pathogenic fungi</subject><subject>Plant roots</subject><subject>Plants</subject><subject>Polymerase Chain Reaction</subject><subject>Receptors</subject><subject>root growth</subject><subject>seedling growth</subject><subject>Seedlings</subject><subject>Signal Transduction</subject><subject>transcription factors</subject><subject>ubiquitin ligase</subject><subject>wei genes</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc1v1DAQxSMEokvhzAWBxQFOaccfcewDh6qigFSJA_RsOYnd9ZLEwXZaVuofX0e76haEZGkO7_eeZ_SK4jWGEww1PZ1GHU-AUQE1YIAnxQqDxCVnEp4WKwBSl4IRdlS8iHEDALIS8Lw4woQDr0m9Ku4u3I1BrR8mP5oxReQtSmuDTFpvezOaMpiYpWjQpNP6Vm-R6zLnrDMdciPSKLbBmBFZH9Ct0b8OTpddY3Rp-WCYk17Ss-Ms6MZ1foouviyeWd1H82o_j4uri88_z7-Wl9-_fDs_uyzbivFUVkIYzaxstWS1EIJQi3Gbn26YYNxWrOaUtg1pCK4JrazVVdc0LdNaGiY5PS4-7XKnuRlM1-YDgu7VFNygw1Z57dTfyujW6trfKFxhVrHs_7D3B_97NjGpwcXW9L0ejZ-jwoILJjBk8P0_4MbPYcy3KQKYUkmoyNDpDmqDjzEY-7AIBrW0qpZW1aHV7Hj7eP8Dv68xAx_3wOI8xIGqFJGSKDv3fTJ_0qOo_5MZeLMDNjH58EBQTCVnOMvvdrLVXunr4KK6-rHclhflAoDTe7usy2U</recordid><startdate>20030304</startdate><enddate>20030304</enddate><creator>Alonso, J.M</creator><creator>Stepanova, A.N</creator><creator>Solano, R</creator><creator>Wisman, E</creator><creator>Ferrari, S</creator><creator>Ausubel, F.M</creator><creator>Ecker, J.R</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><general>The National Academy of Sciences</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20030304</creationdate><title>Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis</title><author>Alonso, J.M ; Stepanova, A.N ; Solano, R ; Wisman, E ; Ferrari, S ; Ausubel, F.M ; Ecker, J.R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-588ea4f9ca94788823f11c11cab4846f547633cb2b217235ffa5dbbc4aa9e4963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>1-aminocyclopropane-1-carboxylic acid</topic><topic>2,4-D</topic><topic>Alleles</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis thaliana</topic><topic>Auxins</topic><topic>Biological Sciences</topic><topic>Botrytis - growth &amp; development</topic><topic>Botrytis - pathogenicity</topic><topic>Botrytis cinerea</topic><topic>ethylene</topic><topic>ethylene receptors</topic><topic>Ethylenes - pharmacology</topic><topic>fungal diseases of plants</topic><topic>Gene Expression Regulation, Plant - drug effects</topic><topic>genes</topic><topic>Genes, Dominant</topic><topic>Genetic Complementation Test</topic><topic>Genetic mutation</topic><topic>Genetic Techniques</topic><topic>Genotype</topic><topic>Hormones</topic><topic>Hypocotyls</topic><topic>ligases</topic><topic>loci</topic><topic>Mitosporic Fungi - growth &amp; development</topic><topic>Mitosporic Fungi - pathogenicity</topic><topic>Models, Genetic</topic><topic>Mutagenesis, Site-Directed</topic><topic>mutants</topic><topic>Mutation</topic><topic>Neurotransmitters</topic><topic>pathogenesis</topic><topic>Phenotypes</topic><topic>Plant Diseases - genetics</topic><topic>Plant Diseases - microbiology</topic><topic>Plant Growth Regulators - pharmacology</topic><topic>plant pathogenic fungi</topic><topic>Plant roots</topic><topic>Plants</topic><topic>Polymerase Chain Reaction</topic><topic>Receptors</topic><topic>root growth</topic><topic>seedling growth</topic><topic>Seedlings</topic><topic>Signal Transduction</topic><topic>transcription factors</topic><topic>ubiquitin ligase</topic><topic>wei genes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alonso, J.M</creatorcontrib><creatorcontrib>Stepanova, A.N</creatorcontrib><creatorcontrib>Solano, R</creatorcontrib><creatorcontrib>Wisman, E</creatorcontrib><creatorcontrib>Ferrari, S</creatorcontrib><creatorcontrib>Ausubel, F.M</creatorcontrib><creatorcontrib>Ecker, J.R</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alonso, J.M</au><au>Stepanova, A.N</au><au>Solano, R</au><au>Wisman, E</au><au>Ferrari, S</au><au>Ausubel, F.M</au><au>Ecker, J.R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2003-03-04</date><risdate>2003</risdate><volume>100</volume><issue>5</issue><spage>2992</spage><epage>2997</epage><pages>2992-2997</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Five ethylene-insensitive loci (wei1-wei5) were identified by using a low-dose screen for "weak" ethylene-insensitive mutants. wei1, wei2, and wei3 seedlings showed hormone insensitivity only in roots, whereas wei4 and wei5 displayed insensitivity in both roots and hypocotyls. The genes corresponding to wei1, wei4, and wei5 were isolated using a positional cloning approach. The wei1 mutant harbored a recessive mutation in TIR1, which encodes a component of the SCF protein ubiquitin ligase involved in the auxin response, wei4, a dominant mutant, resulted from a mutation in the ethylene receptor ERS, whereas wei5, a semidominant mutant, was caused by a mutation in the EIN3-related transcription factor gene EIL1. The simultaneous loss of functional WEI5/EIL1 and EIN3 nearly completely abolished the ethylene response in etiolated seedlings, and adult plants were highly susceptible to infection by the necrotrophic fungal pathogen Botrytis cinerea. Moreover, wei5/eil1 ein3 double mutants were able to fully suppress constitutive signaling caused by ctr1, suggesting a synergistic interaction among these gene products. Unlike previously known root ethylene-insensitive mutants, wei2 and wei3 were not affected in their response to auxin and showed a normal response to gravity. Genetic mapping studies indicate that wei2 and wei3 correspond to previously unidentified ethylene pathway genes that may control cell-elongation processes functioning at the intersection of the ethylene and auxin response pathways.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>12606727</pmid><doi>10.1073/pnas.0438070100</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0027-8424
ispartof Proceedings of the National Academy of Sciences - PNAS, 2003-03, Vol.100 (5), p.2992-2997
issn 0027-8424
1091-6490
language eng
recordid cdi_fao_agris_US201301068006
source MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects 1-aminocyclopropane-1-carboxylic acid
2,4-D
Alleles
Arabidopsis - genetics
Arabidopsis - metabolism
Arabidopsis thaliana
Auxins
Biological Sciences
Botrytis - growth & development
Botrytis - pathogenicity
Botrytis cinerea
ethylene
ethylene receptors
Ethylenes - pharmacology
fungal diseases of plants
Gene Expression Regulation, Plant - drug effects
genes
Genes, Dominant
Genetic Complementation Test
Genetic mutation
Genetic Techniques
Genotype
Hormones
Hypocotyls
ligases
loci
Mitosporic Fungi - growth & development
Mitosporic Fungi - pathogenicity
Models, Genetic
Mutagenesis, Site-Directed
mutants
Mutation
Neurotransmitters
pathogenesis
Phenotypes
Plant Diseases - genetics
Plant Diseases - microbiology
Plant Growth Regulators - pharmacology
plant pathogenic fungi
Plant roots
Plants
Polymerase Chain Reaction
Receptors
root growth
seedling growth
Seedlings
Signal Transduction
transcription factors
ubiquitin ligase
wei genes
title Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T21%3A40%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_fao_a&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Five%20components%20of%20the%20ethylene-response%20pathway%20identified%20in%20a%20screen%20for%20weak%20ethylene-insensitive%20mutants%20in%20Arabidopsis&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Alonso,%20J.M&rft.date=2003-03-04&rft.volume=100&rft.issue=5&rft.spage=2992&rft.epage=2997&rft.pages=2992-2997&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.0438070100&rft_dat=%3Cjstor_fao_a%3E3139641%3C/jstor_fao_a%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=201339238&rft_id=info:pmid/12606727&rft_jstor_id=3139641&rfr_iscdi=true