VIGS vectors for gene silencing: Many targets, many tools

被引:222
作者
Robertson, D [1 ]
机构
[1] N Carolina State Univ, Dept Bot, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Genet, Raleigh, NC 27695 USA
关键词
RNAi; hpRNA; functional genomics; geminiviruses;
D O I
10.1146/annurev.arplant.55.031903.141803
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The discovery that plants recognize and degrade invading viral RNA caused a paradigm shift in our understanding of viral/host interactions. Combined with the discovery that plants cosuppress their own genes if they are transformed with homologous transgenes, new models for both plant intercellular communication and viral defense have emerged. Plant biologists adapted homology-based defense mechanisms triggered by incoming viruses to target individual genes for silencing in a process called virus-induced gene silencing (VIGS). Both VIGS- and dsRNA-containing transformation cassettes are increasingly being used for reverse genetics as part of an integrated approach to determining gene function. Virus-derived vectors silence gene expression without transformation and selection. However, because viruses also alter gene expression in their host, the process of VIGS must be understood. This review examines how DNA and RNA viruses have been modified to silence plant gene expression. I discuss advantages and disadvantages of VIGS in determining gene function and guidelines for the safe use of viral vectors.
引用
收藏
页码:495 / 519
页数:25
相关论文
共 161 条
[1]   Silencing of a gene encoding a protein component of the oxygen-evolving complex of photosystem II enhances virus replication in plants [J].
Abbink, TEM ;
Peart, JR ;
Mos, TNM ;
Baulcombe, DC ;
Bol, JF ;
Linthorst, HJM .
VIROLOGY, 2002, 295 (02) :307-319
[2]   Transcriptional and posttranscriptional plant gene silencing in response to a pathogen [J].
Al-Kaff, NS ;
Covey, SN ;
Kreike, MM ;
Page, AM ;
Pinder, R ;
Dale, PJ .
SCIENCE, 1998, 279 (5359) :2113-2115
[3]   Plants rendered herbicide-susceptible by cauliflower mosaic virus-elicited suppression of a 35S promoter-regulated transgene [J].
Al-Kaff, NS ;
Kreike, MM ;
Covey, SN ;
Pitcher, R ;
Page, AM ;
Dale, PJ .
NATURE BIOTECHNOLOGY, 2000, 18 (09) :995-999
[4]   Use of matrix attachment regions (MARs) to minimize transgene silencing [J].
Allen, GC ;
Spiker, S ;
Thompson, WF .
PLANT MOLECULAR BIOLOGY, 2000, 43 (2-3) :361-376
[5]   A viral suppressor of gene silencing in plants [J].
Anandalakshmi, R ;
Pruss, GJ ;
Ge, X ;
Marathe, R ;
Mallory, AC ;
Smith, TH ;
Vance, VB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13079-13084
[6]  
Angell SM, 1999, PLANT J, V20, P357, DOI 10.1046/j.1365-313X.1999.t01-1-00597.x
[7]   Analysis of trans-silencing interactions using transcriptional silencers of varying strength and targets with and without flanking nuclear matrix attachment regions [J].
Ascenzi, R ;
Ülker, B ;
Todd, JJ ;
Sowinski, DA ;
Schimeneck, CR ;
Allen, GC ;
Weissinger, AK ;
Thompson, WF .
TRANSGENIC RESEARCH, 2003, 12 (03) :305-318
[8]   REGENERATION OF INTACT TOBACCO PLANTS CONTAINING FULL LENGTH COPIES OF GENETICALLY ENGINEERED T-DNA, AND TRANSMISSION OF T-DNA TO R1-PROGENY [J].
BARTON, KA ;
BINNS, AN ;
MATZKE, AJM ;
CHILTON, MD .
CELL, 1983, 32 (04) :1033-1043
[9]  
Bass HW, 2000, J CELL SCI, V113, P1149
[10]   Infection of tobacco or Arabidopsis plants by CMV counteracts systemic post-transcriptional silencing of nonviral (trans)genes [J].
Béclin, C ;
Berthomé, R ;
Palauqui, JC ;
Tepfer, M ;
Vaucheret, H .
VIROLOGY, 1998, 252 (02) :313-317