Lopez-Ochoa Luisa, Ramirez-Prado Jorge, Hanley-Bowdoin Linda
Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC 27695-7622, USA.
J Virol. 2006 Jun;80(12):5841-53. doi: 10.1128/JVI.02698-05.
The AL1 protein of tomato golden mosaic virus (TGMV), a member of the geminivirus family, is essential for viral replication in plants. Its N terminus contains three conserved motifs that mediate origin recognition and DNA cleavage during the initiation of rolling-circle replication. We used the N-terminal domain of TGMV AL1 as bait in a yeast two-hybrid screen of a random peptide aptamer library constrained in the active site of the thioredoxin A (TrxA) gene. The screen selected 88 TrxA peptides that also bind to the full-length TGMV AL1 protein. Plant expression cassettes corresponding to the TrxA peptides and a TGMV A replicon encoding AL1 were cotransfected into tobacco protoplasts, and viral DNA replication was monitored by semiquantitative PCR. In these assays, 31 TrxA peptides negatively impacted TGMV DNA accumulation, reducing viral DNA levels to 13 to 64% of those of the wild type. All of the interfering aptamers also bound to the AL1 protein of cabbage leaf curl virus. A comparison of the 20-mer peptides revealed that their sequences are not random. The alignments detected seven potential binding motifs, five of which are more highly represented among the interfering peptides. One motif was present in 18 peptides, suggesting that these peptides interact with a hot spot in the AL1 N terminus. The peptide aptamers characterized in these studies represent new tools for studying AL1 function and can serve as the basis for the development of crops with broad-based resistance to single-stranded DNA viruses.
番茄金黄花叶病毒(TGMV)是双生病毒科的成员,其AL1蛋白对于病毒在植物中的复制至关重要。它的N端包含三个保守基序,在滚环复制起始过程中介导起始点识别和DNA切割。我们将TGMV AL1的N端结构域作为诱饵,在受硫氧还蛋白A(TrxA)基因活性位点限制的随机肽适配体文库的酵母双杂交筛选中使用。该筛选选出了88个也能与全长TGMV AL1蛋白结合的TrxA肽。将与TrxA肽相对应的植物表达盒和编码AL1的TGMV A复制子共转染到烟草原生质体中,并通过半定量PCR监测病毒DNA复制。在这些试验中,31个TrxA肽对TGMV DNA积累产生负面影响,将病毒DNA水平降低到野生型水平的13%至64%。所有干扰适配体也能与甘蓝叶卷曲病毒的AL1蛋白结合。对20聚体肽的比较表明,它们的序列并非随机。比对检测到七个潜在的结合基序,其中五个在干扰肽中出现的频率更高。一个基序存在于18个肽中,表明这些肽与AL1 N端的一个热点相互作用。这些研究中鉴定的肽适配体代表了研究AL1功能的新工具,可作为开发对单链DNA病毒具有广泛抗性的作物的基础。