烟草花叶病毒侵染烟草差异表达基因的dna - aflp分析

Q3 Agricultural and Biological Sciences Acta Agronomica Sinica Pub Date : 2012-01-01 DOI:10.1016/S1875-2780(11)60099-0
Rong-Ping CHEN , Lie LIU , Xiu-Qing WAN , En-Jian QIU , Chun-Jun WANG , Bao-Gang SONG , Pei-Qiang YAN , Tie-Zhao YANG
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引用次数: 3

摘要

龙江925是一个对烟草花叶病毒(TMV)具有高抗性的烤烟品种。本研究用240对引物扩增了龙江925接种tmv后叶片的cDNA。共获得9500个基因转录片段,通过克隆和测序筛选出12个可诱导表达的基因片段。诱导片段的功能涉及核酸代谢、蛋白质合成与调节、能量代谢、应激反应、细胞内转运和碳水化合物代谢。在接种后0、12、24、48和72 h采集样品,采用实时荧光定量PCR验证差异表达基因序列TIF2的功能。结果表明,TIF2与tmv抗性有关。利用TIF2序列对cDNA末端进行5′和3′快速扩增(RACE),全长cDNA序列长度为875 bp,包含101 ~ 613 bp的可推测编码区,编码170个氨基酸。对Blastn和Blastp基因的分析表明,该基因可能是烟草抗TMV相关的新基因。
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cDNA-AFLP Analysis of Differentially Expressed Genes in Tobacco Infected by Tobacco Mosaic Virus

Longjiang 925 is a flue-cured tobacco variety with high resistance to Tobacco mosaic virus (TMV). In this study, the cDNA extracted from the TMV-inoculated leaves of Longjiang 925 was amplified with 240 pairs of primers. Approximately 9500 gene transcript fragments were obtained, in which 12 inducible expressed gene fragments were selected by cloning and sequencing. The inducible fragments functions involved in the nucleic acid metabolism, protein synthesis and modulation, energy metabolism, stress responding, intracellular transport, and metabolism of carbohydrates. The function of a differentially expressed gene sequence, TIF2, was validated using real-time PCR with the samples collected at 0, 12, 24, 48, and 72 h post inoculation. The result indicated that TIF2 was related to TMV-resistance. Both 5′- and 3′-rapid amplification of cDNA ends (RACE) were preformed using TIF2 sequence, and the full-length cDNA sequence was 875 bp in length, containing a conjecturable coding region from 101 bp to 613 bp and encoding 170 amino acids. Analyses of Blastn and Blastp showed that this gene was probably a novel gene related to TMV resistance in tobacco.

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1.50
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审稿时长
30 weeks
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