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STRESS INDUCED FACTOR 2 Regulates Arabidopsis Stomatal Immunity through Phosphorylation of the Anion Channel SLAC1
SIF2 is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity, belongs to the FLS2/BAK1 immunity receptor complex, and phosphorylates the anion channel SLAC1. Abstract Upon recognition of microbes, pattern recognition receptors (PRRs) activate pattern...
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| Published in: | The Plant cell 2020-07, Vol.32 (7), p.2216-2236 |
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| container_end_page | 2236 |
| container_issue | 7 |
| container_start_page | 2216 |
| container_title | The Plant cell |
| container_volume | 32 |
| creator | Chan, Ching Panzeri, Dario Okuma, Eiji Tõldsepp, Kadri Wang, Ya-Yun Louh, Guan-Yu Chin, Tzu-Chuan Yeh, Yu-Hung Yeh, Hung-Ling Yekondi, Shweta Huang, You-Huei Huang, Tai-Yuan Chiou, Tzyy-Jen Murata, Yoshiyuki Kollist, Hannes Zimmerli, Laurent |
| description | SIF2 is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity, belongs to the FLS2/BAK1 immunity receptor complex, and phosphorylates the anion channel SLAC1.
Abstract
Upon recognition of microbes, pattern recognition receptors (PRRs) activate pattern-triggered immunity. FLAGELLIN SENSING2 (FLS2) and BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) form a typical PRR complex that senses bacteria. Here, we report that the kinase activity of the malectin-like receptor-like kinase STRESS INDUCED FACTOR 2 (SIF2) is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity. SIF2 physically associates with the FLS2-BAK1 PRR complex and interacts with and phosphorylates the guard cell SLOW ANION CHANNEL1 (SLAC1), which is necessary for abscisic acid (ABA)-mediated stomatal closure. SIF2 is also required for the activation of ABA-induced S-type anion currents in Arabidopsis protoplasts, and SIF2 is sufficient to activate SLAC1 anion channels in Xenopus oocytes. SIF2-mediated activation of SLAC1 depends on specific phosphorylation of Ser 65. This work reveals that SIF2 functions between the FLS2-BAK1 initial immunity receptor complex and the final actuator SLAC1 in stomatal immunity. |
| doi_str_mv | 10.1105/tpc.19.00578 |
| format | article |
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Abstract
Upon recognition of microbes, pattern recognition receptors (PRRs) activate pattern-triggered immunity. FLAGELLIN SENSING2 (FLS2) and BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) form a typical PRR complex that senses bacteria. Here, we report that the kinase activity of the malectin-like receptor-like kinase STRESS INDUCED FACTOR 2 (SIF2) is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity. SIF2 physically associates with the FLS2-BAK1 PRR complex and interacts with and phosphorylates the guard cell SLOW ANION CHANNEL1 (SLAC1), which is necessary for abscisic acid (ABA)-mediated stomatal closure. SIF2 is also required for the activation of ABA-induced S-type anion currents in Arabidopsis protoplasts, and SIF2 is sufficient to activate SLAC1 anion channels in Xenopus oocytes. SIF2-mediated activation of SLAC1 depends on specific phosphorylation of Ser 65. This work reveals that SIF2 functions between the FLS2-BAK1 initial immunity receptor complex and the final actuator SLAC1 in stomatal immunity.</description><identifier>ISSN: 1040-4651</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1105/tpc.19.00578</identifier><identifier>PMID: 32327536</identifier><language>eng</language><publisher>England: American Society of Plant Biologists</publisher><subject>Abscisic Acid - metabolism ; Abscisic Acid - pharmacology ; Animals ; Arabidopsis - microbiology ; Arabidopsis - physiology ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - immunology ; Arabidopsis Proteins - metabolism ; Disease Resistance - physiology ; Female ; Histone Deacetylases - genetics ; Histone Deacetylases - immunology ; Histone Deacetylases - metabolism ; Membrane Proteins - genetics ; Membrane Proteins - immunology ; Membrane Proteins - metabolism ; Mutation ; Oocytes - physiology ; Phosphorylation ; Plant Diseases - immunology ; Plant Diseases - microbiology ; Plant Immunity - drug effects ; Plant Stomata - immunology ; Plant Stomata - metabolism ; Plants, Genetically Modified ; Protein Kinases - metabolism ; Protein Serine-Threonine Kinases - metabolism ; Repressor Proteins - genetics ; Repressor Proteins - immunology ; Repressor Proteins - metabolism ; Serine - metabolism ; Xenopus</subject><ispartof>The Plant cell, 2020-07, Vol.32 (7), p.2216-2236</ispartof><rights>2020 American Society of Plant Biologists. All rights reserved. 2020</rights><rights>2020 American Society of Plant Biologists. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-78ef259a968c55a6c8a765c628e23631d4c989c814229fd1182b4de5857ba8b83</citedby><orcidid>0000-0002-5973-2455 ; 0000-0003-3767-5717 ; 0000-0001-9297-4942 ; 0000-0003-3058-7482 ; 0000-0003-1954-0747 ; 0000-0003-4597-8742 ; 0000-0002-6895-3583 ; 0000-0002-3119-6638 ; 0000-0003-1280-4295 ; 0000-0001-5953-4144 ; 0000-0002-7864-1903 ; 0000-0002-8764-6378 ; 0000-0002-3823-2136 ; 0000-0002-5520-3206 ; 0000-0003-1234-5324 ; 0000-0003-0418-0160</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32327536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chan, Ching</creatorcontrib><creatorcontrib>Panzeri, Dario</creatorcontrib><creatorcontrib>Okuma, Eiji</creatorcontrib><creatorcontrib>Tõldsepp, Kadri</creatorcontrib><creatorcontrib>Wang, Ya-Yun</creatorcontrib><creatorcontrib>Louh, Guan-Yu</creatorcontrib><creatorcontrib>Chin, Tzu-Chuan</creatorcontrib><creatorcontrib>Yeh, Yu-Hung</creatorcontrib><creatorcontrib>Yeh, Hung-Ling</creatorcontrib><creatorcontrib>Yekondi, Shweta</creatorcontrib><creatorcontrib>Huang, You-Huei</creatorcontrib><creatorcontrib>Huang, Tai-Yuan</creatorcontrib><creatorcontrib>Chiou, Tzyy-Jen</creatorcontrib><creatorcontrib>Murata, Yoshiyuki</creatorcontrib><creatorcontrib>Kollist, Hannes</creatorcontrib><creatorcontrib>Zimmerli, Laurent</creatorcontrib><title>STRESS INDUCED FACTOR 2 Regulates Arabidopsis Stomatal Immunity through Phosphorylation of the Anion Channel SLAC1</title><title>The Plant cell</title><addtitle>Plant Cell</addtitle><description>SIF2 is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity, belongs to the FLS2/BAK1 immunity receptor complex, and phosphorylates the anion channel SLAC1.
Abstract
Upon recognition of microbes, pattern recognition receptors (PRRs) activate pattern-triggered immunity. FLAGELLIN SENSING2 (FLS2) and BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) form a typical PRR complex that senses bacteria. Here, we report that the kinase activity of the malectin-like receptor-like kinase STRESS INDUCED FACTOR 2 (SIF2) is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity. SIF2 physically associates with the FLS2-BAK1 PRR complex and interacts with and phosphorylates the guard cell SLOW ANION CHANNEL1 (SLAC1), which is necessary for abscisic acid (ABA)-mediated stomatal closure. SIF2 is also required for the activation of ABA-induced S-type anion currents in Arabidopsis protoplasts, and SIF2 is sufficient to activate SLAC1 anion channels in Xenopus oocytes. SIF2-mediated activation of SLAC1 depends on specific phosphorylation of Ser 65. This work reveals that SIF2 functions between the FLS2-BAK1 initial immunity receptor complex and the final actuator SLAC1 in stomatal immunity.</description><subject>Abscisic Acid - metabolism</subject><subject>Abscisic Acid - pharmacology</subject><subject>Animals</subject><subject>Arabidopsis - microbiology</subject><subject>Arabidopsis - physiology</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - immunology</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Disease Resistance - physiology</subject><subject>Female</subject><subject>Histone Deacetylases - genetics</subject><subject>Histone Deacetylases - immunology</subject><subject>Histone Deacetylases - metabolism</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - immunology</subject><subject>Membrane Proteins - metabolism</subject><subject>Mutation</subject><subject>Oocytes - physiology</subject><subject>Phosphorylation</subject><subject>Plant Diseases - immunology</subject><subject>Plant Diseases - microbiology</subject><subject>Plant Immunity - drug effects</subject><subject>Plant Stomata - immunology</subject><subject>Plant Stomata - metabolism</subject><subject>Plants, Genetically Modified</subject><subject>Protein Kinases - metabolism</subject><subject>Protein Serine-Threonine Kinases - metabolism</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - immunology</subject><subject>Repressor Proteins - metabolism</subject><subject>Serine - metabolism</subject><subject>Xenopus</subject><issn>1040-4651</issn><issn>1532-298X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kU1v1DAQhiMEoqVw44x8g0Oz9Ufs2BekKN3CSqsWbbYSN8txnE1QEgfbqbT_HpctFVw4zYzmmXdG8ybJewRXCEF6FWa9QmIFIc35i-QcUYJTLPj3lzGHGUwzRtFZ8sb7HxBClCPxOjkjmOCcEnaeuGq_W1cV2Nxe35fra3BTlPu7HcBgZw7LoILxoHCq7hs7-96DKthRBTWAzTguUx-OIHTOLocOfOusnzvrjnGotxOwbWwZUEyPRdmpaTIDqLZFid4mr1o1ePPuKV4k9zfrffk13d592ZTFNtUZYiHNuWkxFUowrilVTHOVM6oZ5gYTRlCTacGF5ijDWLQNQhzXWWMop3mteM3JRfL5pDsv9Wgababg1CBn14_KHaVVvfy3M_WdPNgHmZP4MyqiwKcnAWd_LsYHOfZem2FQk7GLl5iIjHPKEIno5QnVznrvTPu8BkH5aJOMNkkk5G-bIv7h79Oe4T--RODjCbDL_H-pX4JQmhQ</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Chan, Ching</creator><creator>Panzeri, Dario</creator><creator>Okuma, Eiji</creator><creator>Tõldsepp, Kadri</creator><creator>Wang, Ya-Yun</creator><creator>Louh, Guan-Yu</creator><creator>Chin, Tzu-Chuan</creator><creator>Yeh, Yu-Hung</creator><creator>Yeh, Hung-Ling</creator><creator>Yekondi, Shweta</creator><creator>Huang, You-Huei</creator><creator>Huang, Tai-Yuan</creator><creator>Chiou, Tzyy-Jen</creator><creator>Murata, Yoshiyuki</creator><creator>Kollist, Hannes</creator><creator>Zimmerli, Laurent</creator><general>American Society of Plant Biologists</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5973-2455</orcidid><orcidid>https://orcid.org/0000-0003-3767-5717</orcidid><orcidid>https://orcid.org/0000-0001-9297-4942</orcidid><orcidid>https://orcid.org/0000-0003-3058-7482</orcidid><orcidid>https://orcid.org/0000-0003-1954-0747</orcidid><orcidid>https://orcid.org/0000-0003-4597-8742</orcidid><orcidid>https://orcid.org/0000-0002-6895-3583</orcidid><orcidid>https://orcid.org/0000-0002-3119-6638</orcidid><orcidid>https://orcid.org/0000-0003-1280-4295</orcidid><orcidid>https://orcid.org/0000-0001-5953-4144</orcidid><orcidid>https://orcid.org/0000-0002-7864-1903</orcidid><orcidid>https://orcid.org/0000-0002-8764-6378</orcidid><orcidid>https://orcid.org/0000-0002-3823-2136</orcidid><orcidid>https://orcid.org/0000-0002-5520-3206</orcidid><orcidid>https://orcid.org/0000-0003-1234-5324</orcidid><orcidid>https://orcid.org/0000-0003-0418-0160</orcidid></search><sort><creationdate>20200701</creationdate><title>STRESS INDUCED FACTOR 2 Regulates Arabidopsis Stomatal Immunity through Phosphorylation of the Anion Channel SLAC1</title><author>Chan, Ching ; Panzeri, Dario ; Okuma, Eiji ; Tõldsepp, Kadri ; Wang, Ya-Yun ; Louh, Guan-Yu ; Chin, Tzu-Chuan ; Yeh, Yu-Hung ; Yeh, Hung-Ling ; Yekondi, Shweta ; Huang, You-Huei ; Huang, Tai-Yuan ; Chiou, Tzyy-Jen ; Murata, Yoshiyuki ; Kollist, Hannes ; Zimmerli, Laurent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-78ef259a968c55a6c8a765c628e23631d4c989c814229fd1182b4de5857ba8b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Abscisic Acid - metabolism</topic><topic>Abscisic Acid - pharmacology</topic><topic>Animals</topic><topic>Arabidopsis - microbiology</topic><topic>Arabidopsis - physiology</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - immunology</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Disease Resistance - physiology</topic><topic>Female</topic><topic>Histone Deacetylases - genetics</topic><topic>Histone Deacetylases - immunology</topic><topic>Histone Deacetylases - metabolism</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - immunology</topic><topic>Membrane Proteins - metabolism</topic><topic>Mutation</topic><topic>Oocytes - physiology</topic><topic>Phosphorylation</topic><topic>Plant Diseases - immunology</topic><topic>Plant Diseases - microbiology</topic><topic>Plant Immunity - drug effects</topic><topic>Plant Stomata - immunology</topic><topic>Plant Stomata - metabolism</topic><topic>Plants, Genetically Modified</topic><topic>Protein Kinases - metabolism</topic><topic>Protein Serine-Threonine Kinases - metabolism</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - immunology</topic><topic>Repressor Proteins - metabolism</topic><topic>Serine - metabolism</topic><topic>Xenopus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chan, Ching</creatorcontrib><creatorcontrib>Panzeri, Dario</creatorcontrib><creatorcontrib>Okuma, Eiji</creatorcontrib><creatorcontrib>Tõldsepp, Kadri</creatorcontrib><creatorcontrib>Wang, Ya-Yun</creatorcontrib><creatorcontrib>Louh, Guan-Yu</creatorcontrib><creatorcontrib>Chin, Tzu-Chuan</creatorcontrib><creatorcontrib>Yeh, Yu-Hung</creatorcontrib><creatorcontrib>Yeh, Hung-Ling</creatorcontrib><creatorcontrib>Yekondi, Shweta</creatorcontrib><creatorcontrib>Huang, You-Huei</creatorcontrib><creatorcontrib>Huang, Tai-Yuan</creatorcontrib><creatorcontrib>Chiou, Tzyy-Jen</creatorcontrib><creatorcontrib>Murata, Yoshiyuki</creatorcontrib><creatorcontrib>Kollist, Hannes</creatorcontrib><creatorcontrib>Zimmerli, Laurent</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Plant cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chan, Ching</au><au>Panzeri, Dario</au><au>Okuma, Eiji</au><au>Tõldsepp, Kadri</au><au>Wang, Ya-Yun</au><au>Louh, Guan-Yu</au><au>Chin, Tzu-Chuan</au><au>Yeh, Yu-Hung</au><au>Yeh, Hung-Ling</au><au>Yekondi, Shweta</au><au>Huang, You-Huei</au><au>Huang, Tai-Yuan</au><au>Chiou, Tzyy-Jen</au><au>Murata, Yoshiyuki</au><au>Kollist, Hannes</au><au>Zimmerli, Laurent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>STRESS INDUCED FACTOR 2 Regulates Arabidopsis Stomatal Immunity through Phosphorylation of the Anion Channel SLAC1</atitle><jtitle>The Plant cell</jtitle><addtitle>Plant Cell</addtitle><date>2020-07-01</date><risdate>2020</risdate><volume>32</volume><issue>7</issue><spage>2216</spage><epage>2236</epage><pages>2216-2236</pages><issn>1040-4651</issn><eissn>1532-298X</eissn><abstract>SIF2 is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity, belongs to the FLS2/BAK1 immunity receptor complex, and phosphorylates the anion channel SLAC1.
Abstract
Upon recognition of microbes, pattern recognition receptors (PRRs) activate pattern-triggered immunity. FLAGELLIN SENSING2 (FLS2) and BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) form a typical PRR complex that senses bacteria. Here, we report that the kinase activity of the malectin-like receptor-like kinase STRESS INDUCED FACTOR 2 (SIF2) is critical for Arabidopsis (Arabidopsis thaliana) resistance to bacteria by regulating stomatal immunity. SIF2 physically associates with the FLS2-BAK1 PRR complex and interacts with and phosphorylates the guard cell SLOW ANION CHANNEL1 (SLAC1), which is necessary for abscisic acid (ABA)-mediated stomatal closure. SIF2 is also required for the activation of ABA-induced S-type anion currents in Arabidopsis protoplasts, and SIF2 is sufficient to activate SLAC1 anion channels in Xenopus oocytes. SIF2-mediated activation of SLAC1 depends on specific phosphorylation of Ser 65. This work reveals that SIF2 functions between the FLS2-BAK1 initial immunity receptor complex and the final actuator SLAC1 in stomatal immunity.</abstract><cop>England</cop><pub>American Society of Plant Biologists</pub><pmid>32327536</pmid><doi>10.1105/tpc.19.00578</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-5973-2455</orcidid><orcidid>https://orcid.org/0000-0003-3767-5717</orcidid><orcidid>https://orcid.org/0000-0001-9297-4942</orcidid><orcidid>https://orcid.org/0000-0003-3058-7482</orcidid><orcidid>https://orcid.org/0000-0003-1954-0747</orcidid><orcidid>https://orcid.org/0000-0003-4597-8742</orcidid><orcidid>https://orcid.org/0000-0002-6895-3583</orcidid><orcidid>https://orcid.org/0000-0002-3119-6638</orcidid><orcidid>https://orcid.org/0000-0003-1280-4295</orcidid><orcidid>https://orcid.org/0000-0001-5953-4144</orcidid><orcidid>https://orcid.org/0000-0002-7864-1903</orcidid><orcidid>https://orcid.org/0000-0002-8764-6378</orcidid><orcidid>https://orcid.org/0000-0002-3823-2136</orcidid><orcidid>https://orcid.org/0000-0002-5520-3206</orcidid><orcidid>https://orcid.org/0000-0003-1234-5324</orcidid><orcidid>https://orcid.org/0000-0003-0418-0160</orcidid><oa>free_for_read</oa></addata></record> |
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| ispartof | The Plant cell, 2020-07, Vol.32 (7), p.2216-2236 |
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| source | Oxford Journals Online |
| subjects | Abscisic Acid - metabolism Abscisic Acid - pharmacology Animals Arabidopsis - microbiology Arabidopsis - physiology Arabidopsis Proteins - genetics Arabidopsis Proteins - immunology Arabidopsis Proteins - metabolism Disease Resistance - physiology Female Histone Deacetylases - genetics Histone Deacetylases - immunology Histone Deacetylases - metabolism Membrane Proteins - genetics Membrane Proteins - immunology Membrane Proteins - metabolism Mutation Oocytes - physiology Phosphorylation Plant Diseases - immunology Plant Diseases - microbiology Plant Immunity - drug effects Plant Stomata - immunology Plant Stomata - metabolism Plants, Genetically Modified Protein Kinases - metabolism Protein Serine-Threonine Kinases - metabolism Repressor Proteins - genetics Repressor Proteins - immunology Repressor Proteins - metabolism Serine - metabolism Xenopus |
| title | STRESS INDUCED FACTOR 2 Regulates Arabidopsis Stomatal Immunity through Phosphorylation of the Anion Channel SLAC1 |
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