Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach

Abstract Background Virus-induced gene silencing (VIGS) has been used in many plant species as an attractive post transcriptional gene silencing (PTGS) method for studying gene function either individually or at large-scale in a high-throughput manner. However, the specificity and efficiency for kno...

Full description

Bibliographic Details
Main Authors: Bangjun Zhou, Lirong Zeng
Format: Article
Language:English
Published: BMC 2017-07-01
Series:Plant Methods
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13007-017-0210-6
id doaj-8fadfd2747a949be8fb6adb9862d0bbb
record_format Article
spelling doaj-8fadfd2747a949be8fb6adb9862d0bbb2020-11-25T02:01:41ZengBMCPlant Methods1746-48112017-07-0113111710.1186/s13007-017-0210-6Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approachBangjun Zhou0Lirong Zeng1Center for Plant Science Innovation, Department of Plant Pathology, University of NebraskaCenter for Plant Science Innovation, Department of Plant Pathology, University of NebraskaAbstract Background Virus-induced gene silencing (VIGS) has been used in many plant species as an attractive post transcriptional gene silencing (PTGS) method for studying gene function either individually or at large-scale in a high-throughput manner. However, the specificity and efficiency for knocking down members of a highly homologous gene family have remained to date a significant challenge in VIGS due to silencing of off-targets. Results Here we present an improved method for the selection and evaluation of gene fragments used for VIGS to specifically and efficiently knock down members of a highly homologous gene family. Using this method, we knocked down twelve and four members, respectively of group III of the gene family encoding ubiquitin-conjugating enzymes (E2) in Nicotiana benthamiana. Assays using these VIGS-treated plants revealed that the group III E2s are essential for plant development, plant immunity-associated reactive oxygen species (ROS) production, expression of the gene NbRbohB that is required for ROS production, and suppression of immunity-associated programmed cell death (PCD) by AvrPtoB, an effector protein of the bacterial pathogen Pseudomons syringae. Moreover, functional redundancy for plant development and ROS production was found to exist among members of group III E2s. Conclusions We have found that employment of a gene fragment as short as approximately 70 base pairs (bp) that contains at least three mismatched nucleotides to other genes within any 21-bp sequences prevents silencing of off-target(s) in VIGS. This improved approach in the selection and evaluation of gene fragments allows for specific and efficient knocking down of highly homologous members of a gene family. Using this approach, we implicated N. benthamiana group III E2s in plant development, immunity-associated ROS production, and suppression of multiple immunity-associated PCD by AvrPtoB. We also unraveled functional redundancy among group III members in their requirement for plant development and plant immunity-associated ROS production.http://link.springer.com/article/10.1186/s13007-017-0210-6Virus-induced gene silencingOff-target geneHighly homologous gene familyTobacco rattle virusUbiquitin-conjugating enzymePlant immunity
collection DOAJ
language English
format Article
sources DOAJ
author Bangjun Zhou
Lirong Zeng
spellingShingle Bangjun Zhou
Lirong Zeng
Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach
Plant Methods
Virus-induced gene silencing
Off-target gene
Highly homologous gene family
Tobacco rattle virus
Ubiquitin-conjugating enzyme
Plant immunity
author_facet Bangjun Zhou
Lirong Zeng
author_sort Bangjun Zhou
title Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach
title_short Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach
title_full Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach
title_fullStr Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach
title_full_unstemmed Elucidating the role of highly homologous Nicotiana benthamiana ubiquitin E2 gene family members in plant immunity through an improved virus-induced gene silencing approach
title_sort elucidating the role of highly homologous nicotiana benthamiana ubiquitin e2 gene family members in plant immunity through an improved virus-induced gene silencing approach
publisher BMC
series Plant Methods
issn 1746-4811
publishDate 2017-07-01
description Abstract Background Virus-induced gene silencing (VIGS) has been used in many plant species as an attractive post transcriptional gene silencing (PTGS) method for studying gene function either individually or at large-scale in a high-throughput manner. However, the specificity and efficiency for knocking down members of a highly homologous gene family have remained to date a significant challenge in VIGS due to silencing of off-targets. Results Here we present an improved method for the selection and evaluation of gene fragments used for VIGS to specifically and efficiently knock down members of a highly homologous gene family. Using this method, we knocked down twelve and four members, respectively of group III of the gene family encoding ubiquitin-conjugating enzymes (E2) in Nicotiana benthamiana. Assays using these VIGS-treated plants revealed that the group III E2s are essential for plant development, plant immunity-associated reactive oxygen species (ROS) production, expression of the gene NbRbohB that is required for ROS production, and suppression of immunity-associated programmed cell death (PCD) by AvrPtoB, an effector protein of the bacterial pathogen Pseudomons syringae. Moreover, functional redundancy for plant development and ROS production was found to exist among members of group III E2s. Conclusions We have found that employment of a gene fragment as short as approximately 70 base pairs (bp) that contains at least three mismatched nucleotides to other genes within any 21-bp sequences prevents silencing of off-target(s) in VIGS. This improved approach in the selection and evaluation of gene fragments allows for specific and efficient knocking down of highly homologous members of a gene family. Using this approach, we implicated N. benthamiana group III E2s in plant development, immunity-associated ROS production, and suppression of multiple immunity-associated PCD by AvrPtoB. We also unraveled functional redundancy among group III members in their requirement for plant development and plant immunity-associated ROS production.
topic Virus-induced gene silencing
Off-target gene
Highly homologous gene family
Tobacco rattle virus
Ubiquitin-conjugating enzyme
Plant immunity
url http://link.springer.com/article/10.1186/s13007-017-0210-6
work_keys_str_mv AT bangjunzhou elucidatingtheroleofhighlyhomologousnicotianabenthamianaubiquitine2genefamilymembersinplantimmunitythroughanimprovedvirusinducedgenesilencingapproach
AT lirongzeng elucidatingtheroleofhighlyhomologousnicotianabenthamianaubiquitine2genefamilymembersinplantimmunitythroughanimprovedvirusinducedgenesilencingapproach
_version_ 1724956548093968384