Annamalai Padmanaban, Rao A L N
University of California, Department of Plant Pathology, 3264 Webber Hall, Riverside, CA 925211-0122, USA.
J Virol. 2007 Jan;81(1):173-81. doi: 10.1128/JVI.01500-06. Epub 2006 Sep 27.
The four encapsidated RNAs of brome mosaic virus (BMV; B1, B2, B3, and B4) contain a highly conserved 3' 200-nucleotide (nt) region encompassing the tRNA-like structure (TLS) which is required for packaging in vitro (Y. G. Choi, T. W. Dreher, and A. L. N. Rao, Proc. Natl. Acad. Sci. USA 99:655-660, 2002). To validate these observations in vivo, we performed packaging assays using Agrobacterium-mediated transient expression of RNAs and coat protein (CP) (P. Annamalai and A. L. N. Rao, Virology 338:96-111, 2005). Coexpression of TLS-less constructs of B1 or B2 or B3 and CP mRNAs in Nicotiana benthamiana leaves resulted in packaging of TLS-less B1 and B2 but not B3, suggesting that packaging of B3 requires the TLS in cis. This conjecture was confirmed by the efficient packaging of a B3 chimera in which the viral TLS was replaced with a cellular tRNA(Tyr). When N. benthamiana leaves were infiltrated with a mixture of transformants containing wild-type B1 (wtB1) plus wtB2 plus a TLS-less B3 (wtB1+wtB2+TLS-lessB3), the 3' end of progeny B3 was restored by heterologous recombination with that of either B1 or B2. This intrinsic cis-requirement of TLS in promoting B3 packaging was further confirmed when a mixture containing agrotransformants of TLS-less B1+B2+B3 was supplemented with either wtB4 or a 3' 200-nt or 3' 336-nt untranslated region (UTR) of B3. Northern blot analysis followed by sequencing of B3 progeny revealed that replication of TLS-less B3, but not TLS-less B1 or B2, was fully restored due to recombination with TLS from transiently expressed wtB4 or the B3 3' UTR. Collectively, these observations suggested that the requirement of a cis-acting TLS is distinct for B3 compared with B1 or B2.
雀麦花叶病毒(BMV;B1、B2、B3和B4)的四种衣壳化RNA包含一个高度保守的3'端200个核苷酸(nt)区域,该区域包含体外包装所需的tRNA样结构(TLS)(Y.G. Choi、T.W. Dreher和A.L.N. Rao,《美国国家科学院院刊》99:655 - 660,2002年)。为了在体内验证这些观察结果,我们使用农杆菌介导的RNA和衣壳蛋白(CP)的瞬时表达进行了包装试验(P. Annamalai和A.L.N. Rao,《病毒学》338:96 - 111,2005年)。在本氏烟草叶片中共同表达B1或B2或B3的无TLS构建体与CP mRNA,导致无TLS的B1和B2被包装,但B3未被包装,这表明B3的包装在顺式作用中需要TLS。通过将病毒TLS替换为细胞tRNA(Tyr)的B3嵌合体的有效包装证实了这一推测。当用含有野生型B1(wtB1)加wtB2加无TLS的B3(wtB1 + wtB2 + TLS - lessB3)的转化体混合物浸润本氏烟草叶片时,子代B3的3'端通过与B1或B2的3'端进行异源重组而得以恢复。当含有无TLS的B1 + B2 + B3的农杆菌转化体混合物补充wtB4或B3的3'端200 nt或3'端336 nt非翻译区(UTR)时,TLS在促进B3包装中的这种内在顺式需求得到了进一步证实。Northern印迹分析随后对B3子代进行测序表明,由于与瞬时表达的wtB4或B3 3' UTR的TLS进行重组,无TLS的B3的复制得以完全恢复,但无TLS的B1或B2则不然。总体而言,这些观察结果表明,与B1或B2相比,B3对顺式作用TLS的需求是不同的。