Development of a gene silencing DNA vector derived from a broad host range geminivirus

<p>Abstract</p> <p>Background</p> <p>Gene silencing is proving to be a powerful tool for genetic, developmental, and physiological analyses. The use of viral induced gene silencing (VIGS) offers advantages to transgenic approaches as it can be potentially applied to non...

Full description

Bibliographic Details
Main Authors: Hancock Leandria C, Sather D Noah, Golenberg Edward M, Buckley Kenneth J, Villafranco Natalie M, Bisaro David M
Format: Article
Language:English
Published: BMC 2009-07-01
Series:Plant Methods
Online Access:http://www.plantmethods.com/content/5/1/9
id doaj-0a387b17683a40ba8a73c6f701662d43
record_format Article
spelling doaj-0a387b17683a40ba8a73c6f701662d432020-11-25T00:29:56ZengBMCPlant Methods1746-48112009-07-0151910.1186/1746-4811-5-9Development of a gene silencing DNA vector derived from a broad host range geminivirusHancock Leandria CSather D NoahGolenberg Edward MBuckley Kenneth JVillafranco Natalie MBisaro David M<p>Abstract</p> <p>Background</p> <p>Gene silencing is proving to be a powerful tool for genetic, developmental, and physiological analyses. The use of viral induced gene silencing (VIGS) offers advantages to transgenic approaches as it can be potentially applied to non-model systems for which transgenic techniques are not readily available. However, many VIGS vectors are derived from Gemini viruses that have limited host ranges. We present a new, unipartite vector that is derived from a curtovirus that has a broad host range and will be amenable to use in many non-model systems.</p> <p>Results</p> <p>The construction of a gene silencing vector derived from the geminivirus <it>Beet curly top virus </it>(BCTV), named pWSRi, is reported. Two versions of the vector have been developed to allow application by biolistic techniques or by agro-infiltration. We demonstrate its ability to silence nuclear genes including ribulose bisphosphate carboxylase small subunit (<it>rbcS</it>), <it>transketolase</it>, the sulfur allele of magnesium chelatase (<it>ChlI</it>), and two homeotic transcription factors in spinach or tomato by generating gene-specific knock-down phenotypes. Onset of phenotypes occurred 3 to 12 weeks post-inoculation, depending on the target gene, in organs that developed after the application. The vector lacks movement genes and we found no evidence for significant spread from the site of inoculation. However, viral amplification in inoculated tissue was detected and is necessary for systemic silencing, suggesting that signals generated from active viral replicons are efficiently transported within the plant.</p> <p>Conclusion</p> <p>The unique properties of the pWSRi vector, the ability to silence genes in meristem tissue, the separation of virus and silencing phenotypes, and the broad natural host range of BCTV, suggest that it will have wide utility.</p> http://www.plantmethods.com/content/5/1/9
collection DOAJ
language English
format Article
sources DOAJ
author Hancock Leandria C
Sather D Noah
Golenberg Edward M
Buckley Kenneth J
Villafranco Natalie M
Bisaro David M
spellingShingle Hancock Leandria C
Sather D Noah
Golenberg Edward M
Buckley Kenneth J
Villafranco Natalie M
Bisaro David M
Development of a gene silencing DNA vector derived from a broad host range geminivirus
Plant Methods
author_facet Hancock Leandria C
Sather D Noah
Golenberg Edward M
Buckley Kenneth J
Villafranco Natalie M
Bisaro David M
author_sort Hancock Leandria C
title Development of a gene silencing DNA vector derived from a broad host range geminivirus
title_short Development of a gene silencing DNA vector derived from a broad host range geminivirus
title_full Development of a gene silencing DNA vector derived from a broad host range geminivirus
title_fullStr Development of a gene silencing DNA vector derived from a broad host range geminivirus
title_full_unstemmed Development of a gene silencing DNA vector derived from a broad host range geminivirus
title_sort development of a gene silencing dna vector derived from a broad host range geminivirus
publisher BMC
series Plant Methods
issn 1746-4811
publishDate 2009-07-01
description <p>Abstract</p> <p>Background</p> <p>Gene silencing is proving to be a powerful tool for genetic, developmental, and physiological analyses. The use of viral induced gene silencing (VIGS) offers advantages to transgenic approaches as it can be potentially applied to non-model systems for which transgenic techniques are not readily available. However, many VIGS vectors are derived from Gemini viruses that have limited host ranges. We present a new, unipartite vector that is derived from a curtovirus that has a broad host range and will be amenable to use in many non-model systems.</p> <p>Results</p> <p>The construction of a gene silencing vector derived from the geminivirus <it>Beet curly top virus </it>(BCTV), named pWSRi, is reported. Two versions of the vector have been developed to allow application by biolistic techniques or by agro-infiltration. We demonstrate its ability to silence nuclear genes including ribulose bisphosphate carboxylase small subunit (<it>rbcS</it>), <it>transketolase</it>, the sulfur allele of magnesium chelatase (<it>ChlI</it>), and two homeotic transcription factors in spinach or tomato by generating gene-specific knock-down phenotypes. Onset of phenotypes occurred 3 to 12 weeks post-inoculation, depending on the target gene, in organs that developed after the application. The vector lacks movement genes and we found no evidence for significant spread from the site of inoculation. However, viral amplification in inoculated tissue was detected and is necessary for systemic silencing, suggesting that signals generated from active viral replicons are efficiently transported within the plant.</p> <p>Conclusion</p> <p>The unique properties of the pWSRi vector, the ability to silence genes in meristem tissue, the separation of virus and silencing phenotypes, and the broad natural host range of BCTV, suggest that it will have wide utility.</p>
url http://www.plantmethods.com/content/5/1/9
work_keys_str_mv AT hancockleandriac developmentofagenesilencingdnavectorderivedfromabroadhostrangegeminivirus
AT satherdnoah developmentofagenesilencingdnavectorderivedfromabroadhostrangegeminivirus
AT golenbergedwardm developmentofagenesilencingdnavectorderivedfromabroadhostrangegeminivirus
AT buckleykennethj developmentofagenesilencingdnavectorderivedfromabroadhostrangegeminivirus
AT villafranconataliem developmentofagenesilencingdnavectorderivedfromabroadhostrangegeminivirus
AT bisarodavidm developmentofagenesilencingdnavectorderivedfromabroadhostrangegeminivirus
_version_ 1725328863870844928