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新疆甜菜坏死黄脉病毒RNA5的检测及核苷酸序列分析
引用本文:向本春,刘升学,黄家风,席德慧,吴彩兰.新疆甜菜坏死黄脉病毒RNA5的检测及核苷酸序列分析[J].西北农业学报,2003,12(3):76-80.
作者姓名:向本春  刘升学  黄家风  席德慧  吴彩兰
作者单位:1. 石河子大学农学院农科系,新疆,石河子,832003
2. 石河子大学生物工程学院,新疆,石河子,832003
基金项目:国家自然科学基金项目(39960046);高等学校骨干教师资助项目.
摘    要:利用RT-PCR方法,对12个新疆不同地区的甜菜坏死黄脉病毒(BNYVV)分离物和美国的BN-TX及黑龙江的He分离物进行检测,结果表明,只有库尔勒地区的所有分离物和来自黑龙江的He分离物含有RNA5,其他地区的分离物未检测到RNA5。选K2和He分离物进行序列分析,测得K2分离物长为1323 nt,He分离物长为1300 nt;与国内外报道的中国包头B分离物、呼和浩特H、日本的D5分离物和法国的F72分离物的RNA5序列相比,序列同源性K2为95.0%~96.8%,He为96.0%~99.3%,均含有一个开放阅读框(ORF),由此推导出的各分离物的氨基酸同源性,K2为93.0%~96.5%,He为96.5%~99.6%。其变异主要集中在富含A的区域。

关 键 词:新疆  甜菜坏死黄脉病毒  RNA5  RT-PCR  序列分析
文章编号:1004-1389(2003)03-0076-05
收稿时间:2003/1/3 0:00:00
修稿时间:2003年1月3日

Detection and Nucleotide Sequence Analysis of Beet Necrotic Yellow Vein Virus RNA5 Isolated from Xingjiang
XIANG Ben-chun,LIU Sheng-xue,HUANG Jia-feng,XI De-hui and WU Cai-lan.Detection and Nucleotide Sequence Analysis of Beet Necrotic Yellow Vein Virus RNA5 Isolated from Xingjiang[J].Acta Agriculturae Boreali-occidentalis Sinica,2003,12(3):76-80.
Authors:XIANG Ben-chun  LIU Sheng-xue  HUANG Jia-feng  XI De-hui and WU Cai-lan
Institution:Department of Agronomy Science, College of Agriculture, Shihezi University, Shihezi Xingjiang 832003, China;College of Bio-Engineering, Shihezi University, Shihezi Xingjiang 832003, China;Department of Agronomy Science, College of Agriculture, Shihezi University, Shihezi Xingjiang 832003, China;College of Bio-Engineering, Shihezi University, Shihezi Xingjiang 832003, China;Department of Agronomy Science, College of Agriculture, Shihezi University, Shihezi Xingjiang 832003, China
Abstract:Using RT-PCR method,the RNA5 genomic component waw detected for 12 beet necrotic yellow vein virus (BNYW) isolates from different beet production areas in Xingjiang. The result showed that RNA5 was only found in all kurle isolates and Heilongjiang isolate He,but not in isolates from other areas. Nucleotide sequence were analyzed for K2 and He,the results demonstrated that the RNA5 genome of K2 and He and 1323 nt and 1300 nt in length respectively, which contained single open reading frame(ORF). Comparing with the published sequences of B,H,D5 and F72 isolates,K2 and He isolates shared 95. 0%-96. 8% and 96. 1%-99. 3% nucleotide identity respectively deduced 26 KD protein amino acid identity of K2 and He is 93. 0%-96. 5% and 96. 5%-99. 6% respectively. The variation of genome is mainly in A-rich region.
Keywords:Xinjiang  BNYW  RT-PCR  RNA5  Sequence analysis
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