Saeed Muhammad, Briddon Rob W, Dalakouras Athanasios, Krczal Gabi, Wassenegger Michael
RLP AgroScience GmbH, AlPlanta-Institute for Plant Research, Breitenweg 71, Neustadt D-67435, Germany.
National Institute for Biotechnology and Genetic Engineering, Jhang Road, PO Box 577, Faisalabad 38000, Pakistan.
Biology (Basel). 2015 Oct 23;4(4):697-714. doi: 10.3390/biology4040697.
In South Asia, Cotton leaf curl disease (CLCuD) is caused by a complex of phylogenetically-related begomovirus species and a specific betasatellite, Cotton leaf curl Multan betasatellite (CLCuMuB). The post-transcriptional gene silencing (PTGS) suppression activities of the transcriptional activator protein (TrAP), C4, V2 and βC1 proteins encoded by Cotton leaf curl Kokhran virus (CLCuKoV)/CLCuMuB were assessed in Nicotiana benthamiana. A variable degree of local silencing suppression was observed for each viral protein tested, with V2 protein exhibiting the strongest suppression activity and only the C4 protein preventing the spread of systemic silencing. The CLCuKoV-encoded TrAP, C4, V2 and CLCuMuB-encoded βC1 proteins were expressed in Escherichia coli and purified. TrAP was shown to bind various small and long nucleic acids including single-stranded (ss) and double-stranded (ds) RNA and DNA molecules. C4, V2, and βC1 bound ssDNA and dsDNA with varying affinities. Transgenic expression of C4 under the constitutive 35S Cauliflower mosaic virus promoter and βC1 under a dexamethasone inducible promoter induced severe developmental abnormalities in N. benthamiana. The results indicate that homologous proteins from even quite closely related begomoviruses may differ in their suppressor activity and mechanism of action. The significance of these findings is discussed.
在南亚,棉花曲叶病(CLCuD)由一组系统发育相关的双生病毒物种和一种特定的卫星分子——棉花曲叶木尔坦卫星分子(CLCuMuB)引起。在本氏烟草中评估了由棉花曲叶科赫兰病毒(CLCuKoV)/CLCuMuB编码的转录激活蛋白(TrAP)、C4、V2和βC1蛋白的转录后基因沉默(PTGS)抑制活性。对所测试的每种病毒蛋白都观察到了不同程度的局部沉默抑制,其中V2蛋白表现出最强的抑制活性,只有C4蛋白能阻止系统性沉默的传播。CLCuKoV编码的TrAP、C4、V2和CLCuMuB编码的βC1蛋白在大肠杆菌中表达并纯化。结果表明,TrAP能结合各种小的和长的核酸,包括单链(ss)和双链(ds)RNA及DNA分子。C4、V2和βC1以不同亲和力结合ssDNA和dsDNA。在组成型35S花椰菜花叶病毒启动子控制下的C4转基因表达以及在地塞米松诱导型启动子控制下的βC1转基因表达在本氏烟草中诱导了严重的发育异常。结果表明,即使是亲缘关系相当密切的双生病毒的同源蛋白,其抑制活性和作用机制也可能不同。本文讨论了这些发现的意义。