TY - JOUR
T1 - Differential roles of C4 and βC1 in mediating suppression of post-transcriptional gene silencing
T2 - Evidence for transactivation by the C2 of Bhendi yellow vein mosaic virus, a monopartite begomovirus
AU - Gopal, P.
AU - Pravin Kumar, P.
AU - Sinilal, B.
AU - Jose, J.
AU - Kasin Yadunandam, A.
AU - Usha, R.
N1 - Funding Information:
Funding from CSIR, DBT and UGC Center for Potential in the Subject of Genomic Sciences, are gratefully acknowledged. Instrument and computation facilities from DST-FIST and the Bioinformatics Center, respectively, are acknowledged. We thank Prof. K. Rathore, Institute for Plant Genomics and Biotechnology, Texas for the pBinm-gfp5-ER construct, Prof. K. Veluthambi for pGA643, LBA4404 and pRK2013. We extend our thanks to Dr. D.C. Baulcombe and Dr. Frank Schwach, Sainsbury Laboratory, Norwich, UK for providing GFP16c, gfp silenced GFP16c/GFPi plants and 2b constructs. We are very grateful to Dr. J.C. Carrington, Washington State University, Washington, USA, for providing the Hc-Pro construct. For confocal microscopy we thank the TIFAC CORE and Prof. V.R. Muthukkaruppan of Aravind Medical Research Foundation, Madurai and Ms. Arpitha Parthasarathy for her technical help. We thank Prof. G. Kulandaivelu for the fluorescence microscope facility and Mr. Balakrishnan for the technical help. We thank Ms. K. Vydehi for the pUCNOS construct, and her technical help during the Northern analysis is gratefully acknowledged. Senior Research fellowship to PG, PPK and research associateship to BS from CSIR, India are gratefully acknowledged.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2007/1
Y1 - 2007/1
N2 - Bhendi yellow vein mosaic disease (BYVMD) is caused by the association of a DNA β satellite with a begomovirus component. The begomovirus component has two promoters, one in the virion sense (V-sense) and the other in the complementary sense (C-sense) in the intergenic region (IR). To study the promoter activities of V-sense and C-sense promoters, mGFP gene fusion was made downstream to the promoters. Transient and stable expressions in N. benthamiana leaves showed significant GFP expression under C-sense promoter whereas the expression under the V-sense promoter was very weak in the absence of the transactivator C2. Untransformed N. benthamiana plants were agroinfiltrated with binary vector constructs containing V-sense-GFP alone or along with C1, C2, C4, V1, V2 or βC1 (in both sense and antisense orientations) to understand the roles of these gene products in transactivation and/or suppression of post-transcriptional gene silencing (PTGS). The results showed strong suppression of gene silencing activities for C4 and βC1 but a weak activity for C2. The suppression activities were also confirmed using gfp-silenced GFP16c/GFPi plants by agroinfiltration and agroinoculation. The expression of C4 and βC1 as transgenes produced abnormal phenotypic growth compared to the other viral genes mentioned above, further supporting their suppressor function.
AB - Bhendi yellow vein mosaic disease (BYVMD) is caused by the association of a DNA β satellite with a begomovirus component. The begomovirus component has two promoters, one in the virion sense (V-sense) and the other in the complementary sense (C-sense) in the intergenic region (IR). To study the promoter activities of V-sense and C-sense promoters, mGFP gene fusion was made downstream to the promoters. Transient and stable expressions in N. benthamiana leaves showed significant GFP expression under C-sense promoter whereas the expression under the V-sense promoter was very weak in the absence of the transactivator C2. Untransformed N. benthamiana plants were agroinfiltrated with binary vector constructs containing V-sense-GFP alone or along with C1, C2, C4, V1, V2 or βC1 (in both sense and antisense orientations) to understand the roles of these gene products in transactivation and/or suppression of post-transcriptional gene silencing (PTGS). The results showed strong suppression of gene silencing activities for C4 and βC1 but a weak activity for C2. The suppression activities were also confirmed using gfp-silenced GFP16c/GFPi plants by agroinfiltration and agroinoculation. The expression of C4 and βC1 as transgenes produced abnormal phenotypic growth compared to the other viral genes mentioned above, further supporting their suppressor function.
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U2 - 10.1016/j.virusres.2006.07.014
DO - 10.1016/j.virusres.2006.07.014
M3 - Article
C2 - 16949698
AN - SCOPUS:33751000750
SN - 0168-1702
VL - 123
SP - 9
EP - 18
JO - Virus Research
JF - Virus Research
IS - 1
ER -