Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector

The coat protein (CP) gene cDNA of Grapevine fanleaf virus (GFLV) Hangzhou isolate was amplified from total viral RNA by RT-PCR, then inserted into pGEM-T-easy Vector. Sequence analysis showed that this gene contained 1515 nucleotide acids encoding 504 amino acids. The nucleotide sequence and deduce...

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Main Authors: LI Hong-ye, CHEN Li-geng, Zhou Xue-ping
Format: Article
Language:English
Published: Zhejiang University Press 2002-11-01
Series:浙江大学学报. 农业与生命科学版
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Online Access:https://www.academax.com/doi/10.3785/1008-9209.2002.06.0646
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author LI Hong-ye
CHEN Li-geng
Zhou Xue-ping
author_facet LI Hong-ye
CHEN Li-geng
Zhou Xue-ping
author_sort LI Hong-ye
collection DOAJ
description The coat protein (CP) gene cDNA of Grapevine fanleaf virus (GFLV) Hangzhou isolate was amplified from total viral RNA by RT-PCR, then inserted into pGEM-T-easy Vector. Sequence analysis showed that this gene contained 1515 nucleotide acids encoding 504 amino acids. The nucleotide sequence and deduced amino acid sequence of GFLV-H CP shared, respectively, 88% and 95% identity to those of GFLV-F13. The gene of GFLV-H CP was cloned into plant expression vector pBI121, which was transferred into Agrobacterium tumefaciens LBA4404 by triparental mating.
format Article
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institution Kabale University
issn 1008-9209
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language English
publishDate 2002-11-01
publisher Zhejiang University Press
record_format Article
series 浙江大学学报. 农业与生命科学版
spelling doaj-art-933197a07f7a4b75bda75a42a4bf7a862025-08-20T03:34:08ZengZhejiang University Press浙江大学学报. 农业与生命科学版1008-92092097-51552002-11-012864664810.3785/1008-9209.2002.06.064610089209Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vectorLI Hong-yeCHEN Li-gengZhou Xue-pingThe coat protein (CP) gene cDNA of Grapevine fanleaf virus (GFLV) Hangzhou isolate was amplified from total viral RNA by RT-PCR, then inserted into pGEM-T-easy Vector. Sequence analysis showed that this gene contained 1515 nucleotide acids encoding 504 amino acids. The nucleotide sequence and deduced amino acid sequence of GFLV-H CP shared, respectively, 88% and 95% identity to those of GFLV-F13. The gene of GFLV-H CP was cloned into plant expression vector pBI121, which was transferred into Agrobacterium tumefaciens LBA4404 by triparental mating.https://www.academax.com/doi/10.3785/1008-9209.2002.06.0646<italic>Grapevine fanleaf virus</italic>gene cloningsequence analysis
spellingShingle LI Hong-ye
CHEN Li-geng
Zhou Xue-ping
Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector
浙江大学学报. 农业与生命科学版
<italic>Grapevine fanleaf virus</italic>
gene cloning
sequence analysis
title Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector
title_full Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector
title_fullStr Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector
title_full_unstemmed Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector
title_short Cloning of coat protein gene of Grapevine fanleaf virus Hangzhou isolate and construction of its plant expression vector
title_sort cloning of coat protein gene of grapevine fanleaf virus hangzhou isolate and construction of its plant expression vector
topic <italic>Grapevine fanleaf virus</italic>
gene cloning
sequence analysis
url https://www.academax.com/doi/10.3785/1008-9209.2002.06.0646
work_keys_str_mv AT lihongye cloningofcoatproteingeneofgrapevinefanleafvirushangzhouisolateandconstructionofitsplantexpressionvector
AT chenligeng cloningofcoatproteingeneofgrapevinefanleafvirushangzhouisolateandconstructionofitsplantexpressionvector
AT zhouxueping cloningofcoatproteingeneofgrapevinefanleafvirushangzhouisolateandconstructionofitsplantexpressionvector