2017年第44卷第2期目录
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封面故事:在高等植物中,microRNA作为一类非编码RNA,在调控植物的生长发育、应对生物和非生物的胁迫方面扮演着重要的角色.microRNA模拟靶序列通过竞争性结合miRNA,干扰miRNA对靶标mRNA的调控.前期研究工作发现:黄瓜花叶病毒(CMV)作为miRNA模拟靶序列的表达载体能有效地干扰miRNA的功能;同时,CMV携带的miRNA模拟靶序列与miRNA结合在一定程度上抑制了病毒的积累.为了说明模拟靶序列技术作为抗病毒手段的可行性,杜志游研究组以植物内源的miRNA与其相应的模拟靶序列作为测试对象,通过GFP荧光观察分析二者的体内互作对病毒积累的抑制作用.封面图片中的荧光显微照片清晰地呈现植物内源的miR159、miR162、 miR170与病毒携带的相应模拟靶序列结合,显著降低了GFP的表达,间接说明对病毒积累的抑制;封面图片中的拟南芥植株照片表明CMV携带miR165/166模拟靶序列引起拟南芥表型的改变.该论文的研究结果表明植物内源的miRNA与病毒携带的模拟靶序列结合能有效地抑制病毒的积累,暗示利用模拟靶序列技术,在植物体内表达外源的人造miRNA(Artificial microRNA)分子,靶向病毒基因组的关键位点,有可能建立一种抗病毒的新方法.
(王妹妹,陈文虎,廖乾生,杜志游.MicroRNA靶向病毒携带的microRNA模拟靶序列对病毒的抑制作用,本期第155~162页)
Cover Story:MicroRNA Target Mimics (TM) interfere with regulation of miRNA to its target mRNA by competitively binding the miRNA.Previously, we found that Cucumber mosaic virus (CMV) as a vector expressing a TM sequence effectively inhibited the activity or stability of somemiRNAs in plants, thereby impaired their regulation to the targets.However, the miRNAs binding to their TM sequences carried by CMV inhibited accumulation of the virus to some extent. To analyze underlying reason of the inhibition to virus accumulation when a miRNA binds to its TM sequence in CMV genome, we analyzed influence of various miRNA TM sequences in CMV genome on virus accumulation using RNA blotting.Then, using GFP as a reporter gene, effect of the TM sequences on virus accumulation was analyzed by fluorescence microscopy, Western blotting and RNA blotting.Subsequently, using GFP as a reporter gene again, we analyzed effect of the TM sequences on GFP translation.Finally, the influence of the TM sequences on virus negative-strand RNA synthesis was tested using CMV trans-replication system.The results showed that targeting of five plant endogenous miRNA species tested to their TM sequences carried by CMV genome inhibited virus accumulation to a varied extent.Binding of the miRNAs to their TM sequences suppressed translation of the GFP protein and synthesis of the negative strand. Plant endogenous miRNAs targeting to their target mimics carried by viral genome inhibits translation of viral protein and synthesis of negative strand, thus reduces virus accumulation.The data present here provide possibility for developing a new antiviral methods.
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综述与专论
研究报告
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