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Protein-protein interactions and nuclear trafficking of coat protein and βC1 protein associated with Bhendi yellow vein mosaic disease
Year:
2006
Source of publication :
Virus Research
Authors :
Gafni, Yedidya
;
.
Levy, Yael
;
.
Spanov, Hila
;
.
Zrachya, Avi
;
.
Volume :
122
Co-Authors:
Kumar P., P., Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, 625021, India
Usha, R., Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, 625021, India
Zrachya, A., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Levy, Y., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Spanov, H., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Gafni, Y., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Facilitators :
From page:
127
To page:
136
(
Total pages:
10
)
Abstract:
Bhendi yellow vein mosaic disease (BYVMD) is caused by a complex consisting of a monopartite begomovirus BYVMV and a satellite DNA β component. BYVMV represents a new member of the emerging group of monopartite begomoviruses requiring a satellite component for symptom induction. Here we report the results of the transient expression of green fluorescent protein (GFP) fused with the βC1 and coat protein (CP) coding regions, in the epidermal cells of Nicotiana benthamiana. GFPCP was found to be targeted into the nucleus whereas GFPβC1 was localized towards the periphery of the cell. The sub-cellular localization of the βC1 protein has been compared with that of the CP in yeast cells using a genetic system for detection of protein nuclear import and export. Expression of βC1 ORF in transgenic N. benthamiana under the control of the Cauliflower mosaic virus 35S promoter produced severe developmental abnormalities in the plant, like distorted stem, leaves and stunting of the plant. We also present the results on the interaction of CP and βC1 proteins using yeast two hybrid analysis, suggesting a collaborative role in the inter- and intracellular dynamics of BYVMD. © 2006 Elsevier B.V. All rights reserved.
Note:
Related Files :
Active Transport, Cell Nucleus
gene expression
plant development
Plant Disease
Plant Diseases
Show More
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More details
DOI :
10.1016/j.virusres.2006.07.007
Article number:
0
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
29997
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:51
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Scientific Publication
Protein-protein interactions and nuclear trafficking of coat protein and βC1 protein associated with Bhendi yellow vein mosaic disease
122
Kumar P., P., Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, 625021, India
Usha, R., Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, 625021, India
Zrachya, A., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Levy, Y., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Spanov, H., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Gafni, Y., Department of Genetics, Agricultural Research Organization, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel
Protein-protein interactions and nuclear trafficking of coat protein and βC1 protein associated with Bhendi yellow vein mosaic disease
Bhendi yellow vein mosaic disease (BYVMD) is caused by a complex consisting of a monopartite begomovirus BYVMV and a satellite DNA β component. BYVMV represents a new member of the emerging group of monopartite begomoviruses requiring a satellite component for symptom induction. Here we report the results of the transient expression of green fluorescent protein (GFP) fused with the βC1 and coat protein (CP) coding regions, in the epidermal cells of Nicotiana benthamiana. GFPCP was found to be targeted into the nucleus whereas GFPβC1 was localized towards the periphery of the cell. The sub-cellular localization of the βC1 protein has been compared with that of the CP in yeast cells using a genetic system for detection of protein nuclear import and export. Expression of βC1 ORF in transgenic N. benthamiana under the control of the Cauliflower mosaic virus 35S promoter produced severe developmental abnormalities in the plant, like distorted stem, leaves and stunting of the plant. We also present the results on the interaction of CP and βC1 proteins using yeast two hybrid analysis, suggesting a collaborative role in the inter- and intracellular dynamics of BYVMD. © 2006 Elsevier B.V. All rights reserved.
Scientific Publication
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