The Physcomitrium (Physcomitrella) patens PpKAI2L receptors for strigolactones and related compounds function via MAX2-dependent and -independent pathways

In angiosperms, the α/β hydrolase DWARF14 (D14), along with the F-box protein MORE AXILLARY GROWTH2 (MAX2), perceives strigolactones (SL) to regulate developmental processes. The key SL biosynthetic enzyme CAROTENOID CLEAVAGE DIOXYGENASE8 (CCD8) is present in the moss Physcomitrium patens, and PpCCD...

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Veröffentlicht in:The Plant cell 2021-11, Vol.33 (11), p.3487-3512
Hauptverfasser: Lopez-Obando, Mauricio, Guillory, Ambre, Boyer, François-Didier, Cornu, David, Hoffmann, Beate, Le Bris, Philippe, Pouvreau, Jean-Bernard, Delavault, Philippe, Rameau, Catherine, de Saint Germain, Alexandre, Bonhomme, Sandrine
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container_end_page 3512
container_issue 11
container_start_page 3487
container_title The Plant cell
container_volume 33
creator Lopez-Obando, Mauricio
Guillory, Ambre
Boyer, François-Didier
Cornu, David
Hoffmann, Beate
Le Bris, Philippe
Pouvreau, Jean-Bernard
Delavault, Philippe
Rameau, Catherine
de Saint Germain, Alexandre
Bonhomme, Sandrine
description In angiosperms, the α/β hydrolase DWARF14 (D14), along with the F-box protein MORE AXILLARY GROWTH2 (MAX2), perceives strigolactones (SL) to regulate developmental processes. The key SL biosynthetic enzyme CAROTENOID CLEAVAGE DIOXYGENASE8 (CCD8) is present in the moss Physcomitrium patens, and PpCCD8-derived compounds regulate moss extension. The PpMAX2 homolog is not involved in the SL response, but 13 PpKAI2LIKE (PpKAI2L) genes homologous to the D14 ancestral paralog KARRIKIN INSENSITIVE2 (KAI2) encode candidate SL receptors. In Arabidopsis thaliana, AtKAI2 perceives karrikins and the elusive endogenous KAI2-Ligand (KL). Here, germination assays of the parasitic plant Phelipanche ramosa suggested that PpCCD8-derived compounds are likely noncanonical SLs. (+)-GR24 SL analog is a good mimic for PpCCD8-derived compounds in P. patens, while the effects of its enantiomer (-)-GR24, a KL mimic in angiosperms, are minimal. Interaction and binding assays of seven PpKAI2L proteins pointed to the stereoselectivity toward (-)-GR24 for a single clade of PpKAI2L (eu-KAI2). Enzyme assays highlighted the peculiar behavior of PpKAI2L-H. Phenotypic characterization of Ppkai2l mutants showed that eu-KAI2 genes are not involved in the perception of PpCCD8-derived compounds but act in a PpMAX2-dependent pathway. In contrast, mutations in PpKAI2L-G, and -J genes abolished the response to the (+)-GR24 enantiomer, suggesting that PpKAI2L-G, and -J proteins are receptors for moss SLs.
doi_str_mv 10.1093/plcell/koab217
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The key SL biosynthetic enzyme CAROTENOID CLEAVAGE DIOXYGENASE8 (CCD8) is present in the moss Physcomitrium patens, and PpCCD8-derived compounds regulate moss extension. The PpMAX2 homolog is not involved in the SL response, but 13 PpKAI2LIKE (PpKAI2L) genes homologous to the D14 ancestral paralog KARRIKIN INSENSITIVE2 (KAI2) encode candidate SL receptors. In Arabidopsis thaliana, AtKAI2 perceives karrikins and the elusive endogenous KAI2-Ligand (KL). Here, germination assays of the parasitic plant Phelipanche ramosa suggested that PpCCD8-derived compounds are likely noncanonical SLs. (+)-GR24 SL analog is a good mimic for PpCCD8-derived compounds in P. patens, while the effects of its enantiomer (-)-GR24, a KL mimic in angiosperms, are minimal. Interaction and binding assays of seven PpKAI2L proteins pointed to the stereoselectivity toward (-)-GR24 for a single clade of PpKAI2L (eu-KAI2). Enzyme assays highlighted the peculiar behavior of PpKAI2L-H. Phenotypic characterization of Ppkai2l mutants showed that eu-KAI2 genes are not involved in the perception of PpCCD8-derived compounds but act in a PpMAX2-dependent pathway. In contrast, mutations in PpKAI2L-G, and -J genes abolished the response to the (+)-GR24 enantiomer, suggesting that PpKAI2L-G, and -J proteins are receptors for moss SLs.</description><identifier>ISSN: 1040-4651</identifier><identifier>ISSN: 1532-298X</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1093/plcell/koab217</identifier><identifier>PMID: 34459915</identifier><language>eng</language><publisher>England: American Society of Plant Biologists (ASPB)</publisher><subject>Biochemistry, Molecular Biology ; Botanics ; Botanik ; Botany ; Bryopsida - genetics ; Bryopsida - metabolism ; Bryopsida - parasitology ; Cell Biology ; Cellbiologi ; Heterocyclic Compounds, 3-Ring - metabolism ; Lactones - metabolism ; Life Sciences ; Orobanchaceae - physiology ; Plant Proteins - genetics ; Plant Proteins - metabolism ; Vegetal Biology</subject><ispartof>The Plant cell, 2021-11, Vol.33 (11), p.3487-3512</ispartof><rights>American Society of Plant Biologists 2021. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>American Society of Plant Biologists 2021. All rights reserved. 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The key SL biosynthetic enzyme CAROTENOID CLEAVAGE DIOXYGENASE8 (CCD8) is present in the moss Physcomitrium patens, and PpCCD8-derived compounds regulate moss extension. The PpMAX2 homolog is not involved in the SL response, but 13 PpKAI2LIKE (PpKAI2L) genes homologous to the D14 ancestral paralog KARRIKIN INSENSITIVE2 (KAI2) encode candidate SL receptors. In Arabidopsis thaliana, AtKAI2 perceives karrikins and the elusive endogenous KAI2-Ligand (KL). Here, germination assays of the parasitic plant Phelipanche ramosa suggested that PpCCD8-derived compounds are likely noncanonical SLs. (+)-GR24 SL analog is a good mimic for PpCCD8-derived compounds in P. patens, while the effects of its enantiomer (-)-GR24, a KL mimic in angiosperms, are minimal. Interaction and binding assays of seven PpKAI2L proteins pointed to the stereoselectivity toward (-)-GR24 for a single clade of PpKAI2L (eu-KAI2). Enzyme assays highlighted the peculiar behavior of PpKAI2L-H. Phenotypic characterization of Ppkai2l mutants showed that eu-KAI2 genes are not involved in the perception of PpCCD8-derived compounds but act in a PpMAX2-dependent pathway. 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Guillory, Ambre ; Boyer, François-Didier ; Cornu, David ; Hoffmann, Beate ; Le Bris, Philippe ; Pouvreau, Jean-Bernard ; Delavault, Philippe ; Rameau, Catherine ; de Saint Germain, Alexandre ; Bonhomme, Sandrine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-41d6578e115f050595fc205540ef30eaa18c082d3b792727c15fbadb49df3a763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biochemistry, Molecular Biology</topic><topic>Botanics</topic><topic>Botanik</topic><topic>Botany</topic><topic>Bryopsida - genetics</topic><topic>Bryopsida - metabolism</topic><topic>Bryopsida - parasitology</topic><topic>Cell Biology</topic><topic>Cellbiologi</topic><topic>Heterocyclic Compounds, 3-Ring - metabolism</topic><topic>Lactones - metabolism</topic><topic>Life Sciences</topic><topic>Orobanchaceae - physiology</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - metabolism</topic><topic>Vegetal Biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lopez-Obando, Mauricio</creatorcontrib><creatorcontrib>Guillory, Ambre</creatorcontrib><creatorcontrib>Boyer, François-Didier</creatorcontrib><creatorcontrib>Cornu, David</creatorcontrib><creatorcontrib>Hoffmann, Beate</creatorcontrib><creatorcontrib>Le Bris, Philippe</creatorcontrib><creatorcontrib>Pouvreau, Jean-Bernard</creatorcontrib><creatorcontrib>Delavault, Philippe</creatorcontrib><creatorcontrib>Rameau, Catherine</creatorcontrib><creatorcontrib>de Saint Germain, Alexandre</creatorcontrib><creatorcontrib>Bonhomme, Sandrine</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</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>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>The Plant cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lopez-Obando, Mauricio</au><au>Guillory, Ambre</au><au>Boyer, François-Didier</au><au>Cornu, David</au><au>Hoffmann, Beate</au><au>Le Bris, Philippe</au><au>Pouvreau, Jean-Bernard</au><au>Delavault, Philippe</au><au>Rameau, Catherine</au><au>de Saint Germain, Alexandre</au><au>Bonhomme, Sandrine</au><aucorp>Sveriges lantbruksuniversitet</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Physcomitrium (Physcomitrella) patens PpKAI2L receptors for strigolactones and related compounds function via MAX2-dependent and -independent pathways</atitle><jtitle>The Plant cell</jtitle><addtitle>Plant Cell</addtitle><date>2021-11-04</date><risdate>2021</risdate><volume>33</volume><issue>11</issue><spage>3487</spage><epage>3512</epage><pages>3487-3512</pages><issn>1040-4651</issn><issn>1532-298X</issn><eissn>1532-298X</eissn><abstract>In angiosperms, the α/β hydrolase DWARF14 (D14), along with the F-box protein MORE AXILLARY GROWTH2 (MAX2), perceives strigolactones (SL) to regulate developmental processes. The key SL biosynthetic enzyme CAROTENOID CLEAVAGE DIOXYGENASE8 (CCD8) is present in the moss Physcomitrium patens, and PpCCD8-derived compounds regulate moss extension. The PpMAX2 homolog is not involved in the SL response, but 13 PpKAI2LIKE (PpKAI2L) genes homologous to the D14 ancestral paralog KARRIKIN INSENSITIVE2 (KAI2) encode candidate SL receptors. In Arabidopsis thaliana, AtKAI2 perceives karrikins and the elusive endogenous KAI2-Ligand (KL). Here, germination assays of the parasitic plant Phelipanche ramosa suggested that PpCCD8-derived compounds are likely noncanonical SLs. (+)-GR24 SL analog is a good mimic for PpCCD8-derived compounds in P. patens, while the effects of its enantiomer (-)-GR24, a KL mimic in angiosperms, are minimal. Interaction and binding assays of seven PpKAI2L proteins pointed to the stereoselectivity toward (-)-GR24 for a single clade of PpKAI2L (eu-KAI2). Enzyme assays highlighted the peculiar behavior of PpKAI2L-H. Phenotypic characterization of Ppkai2l mutants showed that eu-KAI2 genes are not involved in the perception of PpCCD8-derived compounds but act in a PpMAX2-dependent pathway. 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source Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Biochemistry, Molecular Biology
Botanics
Botanik
Botany
Bryopsida - genetics
Bryopsida - metabolism
Bryopsida - parasitology
Cell Biology
Cellbiologi
Heterocyclic Compounds, 3-Ring - metabolism
Lactones - metabolism
Life Sciences
Orobanchaceae - physiology
Plant Proteins - genetics
Plant Proteins - metabolism
Vegetal Biology
title The Physcomitrium (Physcomitrella) patens PpKAI2L receptors for strigolactones and related compounds function via MAX2-dependent and -independent pathways
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