Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1

In plants, the actin cytoskeleton plays a critical role in defense against diverse pathogens. The formation of actin patches is essential for the intracellular transport of organelles and molecules toward pathogen penetration sites and the formation of papillae for an early cellular response to powd...

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Main Authors: Peng Gao, Li Qin, Hanh Nguyen, Huajin Sheng, Teagen D. Quilichini, Daoquan Xiang, Leon V. Kochian, Yangdou Wei, Raju Datla
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Plant Science
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fpls.2022.934002/full
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author Peng Gao
Peng Gao
Li Qin
Hanh Nguyen
Huajin Sheng
Teagen D. Quilichini
Daoquan Xiang
Leon V. Kochian
Yangdou Wei
Raju Datla
author_facet Peng Gao
Peng Gao
Li Qin
Hanh Nguyen
Huajin Sheng
Teagen D. Quilichini
Daoquan Xiang
Leon V. Kochian
Yangdou Wei
Raju Datla
author_sort Peng Gao
collection DOAJ
description In plants, the actin cytoskeleton plays a critical role in defense against diverse pathogens. The formation of actin patches is essential for the intracellular transport of organelles and molecules toward pathogen penetration sites and the formation of papillae for an early cellular response to powdery mildew attack in Arabidopsis thaliana. This response process is regulated by the actin-related protein (ARP)2/3 complex and its activator, the WAVE/SCAR complex (W/SRC). The ARP2/3 complex is also required for maintaining steady-state levels of the defense-associated protein, PENETRATION 1 (PEN1), at the plasma membrane and for its deposition into papillae. However, specific ARP2 functionalities in this context remain unresolved, as knockout mutants expressing GFP-PEN1 reporter constructs could not be obtained by conventional crossing approaches. In this study, employing a CRISPR/Cas9 multiplexing-mediated genome editing approach, we produced an ARP2 knockout expressing the GFP-PEN1 marker in Arabidopsis. This study successfully identified diallelic somatic mutations with both ARP2 alleles edited among the primary T1 transgenic plants, and also obtained independent lines with stable arp2/arp2 mutations in the T2 generation. Further analyses on these arp2/arp2 mutants showed similar biological functions of ARP2 to ARP3 in the accumulation of PEN1 against fungal invasion. Together, this CRISPR/Cas9-based approach offers highly efficient simultaneous disruption of the two ARP2 alleles in GFP-PEN1-expressing lines, and a rapid method for performing live-cell imaging to facilitate the investigation of important plant–pathogen interactions using a well-established and widely applied GFP marker system, thus gaining insights and elucidating the contributions of ARP2 upon fungal attack.
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spelling doaj.art-e30169914b584590bae99a71a063c1aa2022-12-22T04:30:47ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2022-09-011310.3389/fpls.2022.934002934002Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1Peng Gao0Peng Gao1Li Qin2Hanh Nguyen3Huajin Sheng4Teagen D. Quilichini5Daoquan Xiang6Leon V. Kochian7Yangdou Wei8Raju Datla9Global Institute for Food Security, University of Saskatchewan, Saskatoon, SK, CanadaAgriculture and Agri-Food Canada, Saskatoon Research and Development Centre, Saskatoon, SK, CanadaGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, SK, CanadaGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, SK, CanadaGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, SK, CanadaAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, SK, CanadaAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, SK, CanadaGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, SK, CanadaCollege of Arts and Science, University of Saskatchewan, Saskatoon, SK, CanadaGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, SK, CanadaIn plants, the actin cytoskeleton plays a critical role in defense against diverse pathogens. The formation of actin patches is essential for the intracellular transport of organelles and molecules toward pathogen penetration sites and the formation of papillae for an early cellular response to powdery mildew attack in Arabidopsis thaliana. This response process is regulated by the actin-related protein (ARP)2/3 complex and its activator, the WAVE/SCAR complex (W/SRC). The ARP2/3 complex is also required for maintaining steady-state levels of the defense-associated protein, PENETRATION 1 (PEN1), at the plasma membrane and for its deposition into papillae. However, specific ARP2 functionalities in this context remain unresolved, as knockout mutants expressing GFP-PEN1 reporter constructs could not be obtained by conventional crossing approaches. In this study, employing a CRISPR/Cas9 multiplexing-mediated genome editing approach, we produced an ARP2 knockout expressing the GFP-PEN1 marker in Arabidopsis. This study successfully identified diallelic somatic mutations with both ARP2 alleles edited among the primary T1 transgenic plants, and also obtained independent lines with stable arp2/arp2 mutations in the T2 generation. Further analyses on these arp2/arp2 mutants showed similar biological functions of ARP2 to ARP3 in the accumulation of PEN1 against fungal invasion. Together, this CRISPR/Cas9-based approach offers highly efficient simultaneous disruption of the two ARP2 alleles in GFP-PEN1-expressing lines, and a rapid method for performing live-cell imaging to facilitate the investigation of important plant–pathogen interactions using a well-established and widely applied GFP marker system, thus gaining insights and elucidating the contributions of ARP2 upon fungal attack.https://www.frontiersin.org/articles/10.3389/fpls.2022.934002/fullCRISPR/Cas9actin-related proteindiallelic mutantssomatic mutationsplant pathogen interactions
spellingShingle Peng Gao
Peng Gao
Li Qin
Hanh Nguyen
Huajin Sheng
Teagen D. Quilichini
Daoquan Xiang
Leon V. Kochian
Yangdou Wei
Raju Datla
Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1
Frontiers in Plant Science
CRISPR/Cas9
actin-related protein
diallelic mutants
somatic mutations
plant pathogen interactions
title Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1
title_full Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1
title_fullStr Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1
title_full_unstemmed Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1
title_short Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9-generated diallelic mutants reveal Arabidopsis actin-related protein 2 function in the trafficking of syntaxin PEN1
title_sort clustered regularly interspaced short palindromic repeats crispr associated protein 9 generated diallelic mutants reveal arabidopsis actin related protein 2 function in the trafficking of syntaxin pen1
topic CRISPR/Cas9
actin-related protein
diallelic mutants
somatic mutations
plant pathogen interactions
url https://www.frontiersin.org/articles/10.3389/fpls.2022.934002/full
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