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The Cloning and Sequencing of Read-through Protein Gene from BYDV-GAV Virus

CHANG Sheng-jun WANG Xi-feng LI Li MA Zhan-hong ZHOU Guang-he

中国农业科学(英文版)Issue(1):45-49,5.
中国农业科学(英文版)Issue(1):45-49,5.

The Cloning and Sequencing of Read-through Protein Gene from BYDV-GAV Virus

The Cloning and Sequencing of Read-through Protein Gene from BYDV-GAV Virus

CHANG Sheng-jun 1WANG Xi-feng 1LI Li 1MA Zhan-hong 1ZHOU Guang-he1

作者信息

  • 1. State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Acaderny of Agricultural Sciences, Beijing 100094
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摘要

Abstract

The cDNA of BYDV-GAV read-through protein (RTP) gene was amplified from the extracted RNA of BYDV-GAV by using the polymerase chain reaction (PCR), and cloned into pGEM-7zf( + ). Its complete nucleotide sequence was determined by dideoxynucleotide chain-termination method. The BYDV-GAV RTP gene consists of 1377nt. Its sequences were most similar to that of the RTP gene of BYDV - MAV with identities of 87.4% and 87.1% at the nucleotide and amino acid levels, respectively.

关键词

BYDV-GAV/Read-through protein gene/Sequence

Key words

BYDV-GAV/Read-through protein gene/Sequence

分类

农业科技

引用本文复制引用

CHANG Sheng-jun,WANG Xi-feng,LI Li,MA Zhan-hong,ZHOU Guang-he..The Cloning and Sequencing of Read-through Protein Gene from BYDV-GAV Virus[J].中国农业科学(英文版),2001,(1):45-49,5.

基金项目

This work is supported by the National Key Basic Research (Project 973 No. G2000016201), and National Natural Science Foundation of China (39970034). (Project 973 No. G2000016201)

中国农业科学(英文版)

2095-3119

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