期刊论文详细信息
Plant Methods
Method: low-cost delivery of the cotton leaf crumple virus-induced gene silencing system
Dominique Robertson2  Candace H Haigler2  John Richard Tuttle1 
[1] Department of Crop Science, North Carolina State University, Raleigh, NC 27695, USA;Department of Plant Biology, North Carolina State University, Raleigh, NC 27695, USA
关键词: Gossypium;    Bombardment;    Particle inflow gun;    Agroinoculation;    Cotton leaf crumple virus;    Virus-induced gene silencing;    VIGS;    Cotton;   
Others  :  821953
DOI  :  10.1186/1746-4811-8-27
 received in 2012-04-23, accepted in 2012-07-19,  发布年份 2012
PDF
【 摘 要 】

Background

We previously developed a virus-induced gene silencing (VIGS) vector for cotton from the bipartite geminivirusCotton leaf crumple virus (CLCrV). The original CLCrV VIGS vector was designed for biolistic delivery by a gene gun. This prerequisite limited the use of the system to labs with access to biolistic equipment. Here we describe the adaptation of this system for delivery by Agrobacterium (Agrobacterium tumefaciens). We also describe the construction of two low-cost particle inflow guns.

Results

The biolistic CLCrV vector was transferred into two Agrobacterium binary plasmids. Agroinoculation of the binary plasmids into cotton resulted in silencing and GFP expression comparable to the biolistic vector. Two homemade low-cost gene guns were used to successfully inoculate cotton (G. hirsutum) and N. benthamiana with either the CLCrV VIGS vector or the Tomato golden mosaic virus (TGMV) VIGS vector respectively.

Conclusions

These innovations extend the versatility of CLCrV-based VIGS for analyzing gene function in cotton. The two low-cost gene guns make VIGS experiments affordable for both research and teaching labs by providing a working alternative to expensive commercial gene guns.

【 授权许可】

   
2012 Tuttle et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140712091025133.pdf 1567KB PDF download
Figure 5 . 40KB Image download
Figure 4 . 30KB Image download
Figure 3 . 131KB Image download
Figure 2 . 27KB Image download
Figure 1 . 63KB Image download
【 图 表 】

Figure 1 .

Figure 2 .

Figure 3 .

Figure 4 .

Figure 5 .

【 参考文献 】
  • [1]Burch-Smith TM, Anderson JC, Martin GB, Dinesh-Kumar SP: Applications and advantages of virus-induced gene silencing for gene function studies in plants. Plant J 2004, 39:734-746.
  • [2]Carrillo-Tripp J, Shimada-Beltran H, Rivera-Bustamante R: Use of geminiviral vectors for functional genomics. Curr Opin Plant Biol 2006, 9:209-215.
  • [3]Robertson D: VIGS vectors for gene silencing: many targets, many tools. Annu Rev Plant Biol 2004, 55:495-519.
  • [4]Davies JW, Stanley J: Geminivirus genes and vectors. Trends Genet 1989, 5:77-81.
  • [5]Laufs J, Traut W, Heyraud F, Matzeit V, Rogers SG, Schell J, Gronenborn B: In vitro cleavage and joining at the viral origin of replication by the replication initiator protein of tomato yellow leaf curl virus. Proc Natl Acad Sci U S A 1995, 92:3879-3883.
  • [6]Preiss W, Jeske H: Multitasking in replication is common among geminiviruses. J Virol 2003, 77:2972-2980.
  • [7]Rogers SG, Bisaro DM, Horsch RB, Fraley RT, Hoffmann NL, Brand L, Elmer JS, Lloyd AM: Tomato golden mosaic virus A component DNA replicates autonomously in transgenic plants. Cell 1986, 45:593-600.
  • [8]Stenger DC, Revington GN, Stevenson MC, Bisaro DM: Replicational release of geminivirus genomes from tandemly repeated copies: evidence for rolling-circle replication of a plant viral DNA. Proc Natl Acad Sci U S A 1991, 88:8029-8033.
  • [9]Peele C, Jordan CV, Muangsan N, Turnage M, Egelkrout E, Eagle P, Hanley-Bowdoin L, Robertson D: Silencing of a meristematic gene using geminivirus-derived vectors. Plant J 2001, 27:357-366.
  • [10]Turnage MA, Muangsan N, Peele CG, Robertson D: Geminivirus-based vectors for gene silencing in Arabidopsis. Plant J 2002, 30:107-114.
  • [11]Fofana IB, Sangare A, Collier R, Taylor C, Fauquet CM: A geminivirus-induced gene silencing system for gene function validation in cassava. Plant Mol Biol 2004, 56:613-624.
  • [12]Tuttle JR, Idris AM, Brown JK, Haigler CH, Robertson D: Geminivirus-mediated gene silencing from Cotton leaf crumple virus is enhanced by low temperature in cotton. Plant Physiol 2008, 148:41-50.
  • [13]Briddon RW, Watts J, Markham PG, Stanley J: The coat protein of beet curly top virus is essential for infectivity. Virology 1989, 172:628-633.
  • [14]Azzam O, Frazer J, de la Rosa D, Beaver JS, Ahlquist P, Maxwell DP: Whitefly transmission and efficient ssDNA accumulation of bean golden mosaic geminivirus require functional coat protein. Virology 1994, 204:289-296.
  • [15]Finer JJ, Vain P, Jones MW, McMullen MD: Development of the particle inflow gun for DNA delivery to plant cells. Plant Cell Rep 1992, 11:323-328.
  • [16]Vain PK, Keen N, Murillo J, Rathus C, Nemes C, Finer J: Development of the Particle Inflow Gun. Plant Cell, Tissue and Organ Culture 1993, 33:237-246.
  • [17]Gal-On A, Meiri E, Elman C, Gray DJ, Gaba V: Simple hand-held devices for the efficient infection of plants with viral-encoding constructs by particle bombardment. J Virol Methods 1997, 64:103-110.
  • [18]Ascencio-Ibanez JT, Settlage SB: DNA abrasion onto plants is an effective method for geminivirus infection and virus-induced gene silencing. J Virol Methods 2007, 142:198-203.
  • [19]Rojas MR, Hagen C, Lucas WJ, Gilbertson RL: Exploiting chinks in the plant's armor: evolution and emergence of geminiviruses. Annu Rev Phytopathol 2005, 43:361-394.
  • [20]Elmer JS, Sunter G, Gardiner WE, Brand L, Browning CK, Bisaro DM, Rogers SG: Agrobacterium-mediated inoculation of plants with tomato golden mosaic virus DNAs. Plant Mol Biol 1988, 10:225-234.
  • [21]Briddon RW, Mansoor S, Bedford ID, Pinner MS, Markham PG: Clones of cotton leaf curl geminivirus induce symptoms atypical of cotton leaf curl disease. Virus Genes 2000, 20:19-26.
  • [22]Gao S, Qu J, Chua NH, Ye J: A new strain of Indian cassava mosaic virus causes a mosaic disease in the biodiesel crop Jatrophacurcas. Arch Virol 2010, 155:607-612.
  • [23]Brown JN, Nelson MR: Host range and vector relationships of Cotton leaf crumple virus. Plant Dis 1987, 71:522-524.
  • [24]Brown JN, Nelson MR: Geminate particles associated with cotton leaf crumple disease in Arizona. Phytopathology 1984, 74:987-990.
  • [25]Idris AM, Tuttle JR, Robertson D, Haigler CH, Brown JK: Differential Cotton leaf crumple virus-VIGS-mediated gene silencing and viral genome localization in different Gossypiumhirsutum genetic backgrounds. Physiol Mol Plant Pathol 2010, 75:13-22.
  • [26]Koncz CS, Schell J: The promoter of TL-DNA gene 5 controls the tissue-specific expression of chimaeric genes carried by a novel type ofAgrobacteriumbinary vector. Mol Gen Genet 1986, 204:383-396.
  • [27]Hofgen R, Willmitzer L: Storage of competent cells for Agrobacteriumtransformation. Nucleic Acids Res 1988, 16:9877.
  • [28]Davis SJ, Vierstra RD: Soluble, highly fluorescent variants of green fluorescent protein (GFP) for use in higher plants. Plant Mol Biol 1998, 36:521-528.
  • [29]Lacroix B, Vaidya M, Tzfira T, Citovsky V: The VirE3 protein ofAgrobacterium mimics a host cell function required for plant genetic transformation. EMBO J 2005, 24:428-437.
  • [30]Veena , Jiang H, Doerge RW, Gelvin SB: Transfer of T-DNA and Vir proteins to plant cells byAgrobacteriumtumefaciens induces expression of host genes involved in mediating transformation and suppresses host defense gene expression. Plant J 2003, 35:219-236.
  • [31]Idris AM, Brown JK: Cotton leaf crumple virusis a distinct western hemisphere begomovirus species with complex evolutionary relationships indicative of recombination and reassortment. Phytopathology 2004, 94:1068-1074.
  • [32]Burch-Smith TM, Schiff M, Liu Y, Dinesh-Kumar SP: Efficient Virus-Induced Gene Silencing in Arabidopsis. Plant Physiol 2006, 142:21-27.
  文献评价指标  
  下载次数:114次 浏览次数:12次