Cargando…
Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins
MonocotJRLs are Poaceae-specific two-domain proteins that consist of a jacalin-related lectin (JRL) and a dirigent (DIR) domain which participate in multiple developmental processes, including disease resistance. For OsJAC1, a monocotJRL from rice, it has been confirmed that constitutive expression...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824508/ https://www.ncbi.nlm.nih.gov/pubmed/36616196 http://dx.doi.org/10.3390/plants12010067 |
_version_ | 1784866427480571904 |
---|---|
author | Esch, Lara Kirsch, Christian Vogel, Lara Kelm, Jana Huwa, Nikolai Schmitz, Maike Classen, Thomas Schaffrath, Ulrich |
author_facet | Esch, Lara Kirsch, Christian Vogel, Lara Kelm, Jana Huwa, Nikolai Schmitz, Maike Classen, Thomas Schaffrath, Ulrich |
author_sort | Esch, Lara |
collection | PubMed |
description | MonocotJRLs are Poaceae-specific two-domain proteins that consist of a jacalin-related lectin (JRL) and a dirigent (DIR) domain which participate in multiple developmental processes, including disease resistance. For OsJAC1, a monocotJRL from rice, it has been confirmed that constitutive expression in transgenic rice or barley plants facilitates broad-spectrum disease resistance. In this process, both domains of OsJAC1 act cooperatively, as evidenced from experiments with artificially separated JRL- or DIR-domain-containing proteins. Interestingly, these chimeric proteins did not evolve in dicotyledonous plants. Instead, proteins with a single JRL domain, multiple JRL domains or JRL domains fused to domains other than DIR domains are present. In this study, we wanted to test if the cooperative function of JRL and DIR proteins leading to pathogen resistance was conserved in the dicotyledonous plant Arabidopsis thaliana. In Arabidopsis, we identified 50 JRL and 24 DIR proteins, respectively, from which seven single-domain JRL and two single-domain DIR candidates were selected. A single-cell transient gene expression assay in barley revealed that specific combinations of the Arabidopsis JRL and DIR candidates reduced the penetration success of barley powdery mildew. Strikingly, one of these pairs, AtJAX1 and AtDIR19, is encoded by genes located next to each other on chromosome one. However, when using natural variation and analyzing Arabidopsis ecotypes that express full-length or truncated versions of AtJAX1, the presence/absence of the full-length AtJAX1 protein could not be correlated with resistance to the powdery mildew fungus Golovinomyces orontii. Furthermore, an analysis of the additional JRL and DIR candidates in a bi-fluorescence complementation assay in Nicotiana benthamiana revealed no direct interaction of these JRL/DIR pairs. Since transgenic Arabidopsis plants expressing OsJAC1-GFP also did not show increased resistance to G. orontii, it was concluded that the resistance mediated by the synergistic activities of DIR and JRL proteins is specific for members of the Poaceae, at least regarding the resistance against powdery mildew. Arabidopsis lacks the essential components of the DIR-JRL-dependent resistance pathway. |
format | Online Article Text |
id | pubmed-9824508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98245082023-01-08 Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins Esch, Lara Kirsch, Christian Vogel, Lara Kelm, Jana Huwa, Nikolai Schmitz, Maike Classen, Thomas Schaffrath, Ulrich Plants (Basel) Article MonocotJRLs are Poaceae-specific two-domain proteins that consist of a jacalin-related lectin (JRL) and a dirigent (DIR) domain which participate in multiple developmental processes, including disease resistance. For OsJAC1, a monocotJRL from rice, it has been confirmed that constitutive expression in transgenic rice or barley plants facilitates broad-spectrum disease resistance. In this process, both domains of OsJAC1 act cooperatively, as evidenced from experiments with artificially separated JRL- or DIR-domain-containing proteins. Interestingly, these chimeric proteins did not evolve in dicotyledonous plants. Instead, proteins with a single JRL domain, multiple JRL domains or JRL domains fused to domains other than DIR domains are present. In this study, we wanted to test if the cooperative function of JRL and DIR proteins leading to pathogen resistance was conserved in the dicotyledonous plant Arabidopsis thaliana. In Arabidopsis, we identified 50 JRL and 24 DIR proteins, respectively, from which seven single-domain JRL and two single-domain DIR candidates were selected. A single-cell transient gene expression assay in barley revealed that specific combinations of the Arabidopsis JRL and DIR candidates reduced the penetration success of barley powdery mildew. Strikingly, one of these pairs, AtJAX1 and AtDIR19, is encoded by genes located next to each other on chromosome one. However, when using natural variation and analyzing Arabidopsis ecotypes that express full-length or truncated versions of AtJAX1, the presence/absence of the full-length AtJAX1 protein could not be correlated with resistance to the powdery mildew fungus Golovinomyces orontii. Furthermore, an analysis of the additional JRL and DIR candidates in a bi-fluorescence complementation assay in Nicotiana benthamiana revealed no direct interaction of these JRL/DIR pairs. Since transgenic Arabidopsis plants expressing OsJAC1-GFP also did not show increased resistance to G. orontii, it was concluded that the resistance mediated by the synergistic activities of DIR and JRL proteins is specific for members of the Poaceae, at least regarding the resistance against powdery mildew. Arabidopsis lacks the essential components of the DIR-JRL-dependent resistance pathway. MDPI 2022-12-23 /pmc/articles/PMC9824508/ /pubmed/36616196 http://dx.doi.org/10.3390/plants12010067 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Esch, Lara Kirsch, Christian Vogel, Lara Kelm, Jana Huwa, Nikolai Schmitz, Maike Classen, Thomas Schaffrath, Ulrich Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins |
title | Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins |
title_full | Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins |
title_fullStr | Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins |
title_full_unstemmed | Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins |
title_short | Pathogen Resistance Depending on Jacalin-Dirigent Chimeric Proteins Is Common among Poaceae but Absent in the Dicot Arabidopsis as Evidenced by Analysis of Homologous Single-Domain Proteins |
title_sort | pathogen resistance depending on jacalin-dirigent chimeric proteins is common among poaceae but absent in the dicot arabidopsis as evidenced by analysis of homologous single-domain proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824508/ https://www.ncbi.nlm.nih.gov/pubmed/36616196 http://dx.doi.org/10.3390/plants12010067 |
work_keys_str_mv | AT eschlara pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT kirschchristian pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT vogellara pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT kelmjana pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT huwanikolai pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT schmitzmaike pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT classenthomas pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins AT schaffrathulrich pathogenresistancedependingonjacalindirigentchimericproteinsiscommonamongpoaceaebutabsentinthedicotarabidopsisasevidencedbyanalysisofhomologoussingledomainproteins |