scholarly journals Soybean Mosaic Virus Resistance in Transgenic Soybean Caused by Post-transcriptional Gene Silencing

2007 ◽  
Vol 57 (2) ◽  
pp. 123-128 ◽  
Author(s):  
Noriyuki Furutani ◽  
Noriko Yamagishi ◽  
Soh Hidaka ◽  
Yoshiaki Shizukawa ◽  
Seiji Kanematsu ◽  
...  
2008 ◽  
Vol 18 (3) ◽  
pp. 331-345 ◽  
Author(s):  
Marina Brumin ◽  
Svetlana Stukalov ◽  
Sabrina Haviv ◽  
Mookkan Muruganantham ◽  
Yoni Moskovitz ◽  
...  

Microbiology ◽  
2000 ◽  
Vol 81 (1) ◽  
pp. 235-242 ◽  
Author(s):  
Fuh-Jyh Jan ◽  
Carmen Fagoaga ◽  
Sheng-Zhi Pang ◽  
Dennis Gonsalves

We showed previously that transgenic plants with the green fluorescent protein (GFP) gene fused to segments of the nucleocapsid (N) gene of tomato spotted wilt virus (TSWV) displayed post-transcriptional gene silencing of the GFP and N gene segments and resistance to TSWV. These results suggested that a chimeric transgene composed of viral gene segments might confer multiple virus resistance in transgenic plants. To test this hypothesis and to determine the minimum length of the N gene that could trans-inactivate the challenging TSWV, transgenic plants were developed that contained GFP fused with N gene segments of 24–453 bp. Progeny from these plants were challenged with: (i) a chimeric tobacco mosaic virus containing the GFP gene, (ii) a chimeric tobacco mosaic virus with GFP plus the N gene of TSWV and (iii) TSWV. A number of transgenic plants expressing the transgene with GFP fused to N gene segments from 110 to 453 bp in size were resistant to these viruses. Resistant plants exhibited post-transcriptional gene silencing. In contrast, all transgenic lines with transgenes consisting of GFP fused to N gene segments of 24 or 59 bp were susceptible to TSWV, even though the transgene was post-transcriptionally silenced. Thus, virus resistance and post-transcriptional gene silencing were uncoupled when the N gene segment was 59 bp or less. These results provide evidence that multiple virus resistance is possible through the simple strategy of linking viral gene segments to a silencer DNA such as GFP.


2002 ◽  
Vol 14 (3) ◽  
pp. 629-639 ◽  
Author(s):  
Jean-Benoit Morel ◽  
Christian Godon ◽  
Philippe Mourrain ◽  
Christophe Béclin ◽  
Stéphanie Boutet ◽  
...  

2006 ◽  
Vol 23 (3) ◽  
pp. 259-265 ◽  
Author(s):  
Shungo Otagaki ◽  
Makoto Arai ◽  
Akiko Takahashi ◽  
Kazunori Goto ◽  
Jin-Sung Hong ◽  
...  

2002 ◽  
Vol 15 (8) ◽  
pp. 753-763 ◽  
Author(s):  
Ezequiel Balmori-Melian ◽  
Robin M. MacDiarmid ◽  
David L. Beck ◽  
Richard C. Gardner ◽  
Richard L. S. Forster

Transgenic Nicotiana benthamiana plants expressing an untranslatable version of the coat protein (CP) gene from the Tamarillo mosaic virus (TaMV) were either resistant to TaMV infection or recovered from infection. These phenotypes were the result of a post-transcriptional gene silencing (PTGS) mechanism that targeted TaMV-CP sequences for degradation. The TaMV-CP sequences were degraded when present in the wild-type TaMV potyvirus, in transgene mRNA, or in chimeric viral vectors based on White clover mosaic virus. The more efficiently targeted region was mapped to a 134-nt segment. Differences were observed in the efficiency of targeting during cell-to-cell and long-distance movement of the chimeric viruses. However, the TaMV-CP sequences do not appear to be targeted for degradation when delivered by biolistics.


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