Blanchard C L, Boyce P M, Anderson B J
School of Science and Technology, Charles Sturt University, Wagga Wagga, NSW, Australia.
Virology. 1996 Mar 15;217(2):598-601. doi: 10.1006/viro.1996.0155.
Analysis of encapsidated RNA from the Q strain of CMV (Q-CMV) has indicated the presence of a discreet population of molecules of approximately 300 nt termed RNA 5 (Peden, K.W.C., and Symons, R.H., Virology 53,487-492, 1973.). Q-CMV RNA 5 was isolated and the 5'-end sequence was determined by direct RNA sequencing. This sequence corresponded to the exact beginning of the imperfectly conserved 3'-terminal region of genomic RNAs 1, 2, and 3. A probe generated from RNA 3 consisting of the last 130 nt of this region hybridised to RNA 5. Oligonucleotides containing sequences from the 5'- and 3'-ends of the conserved region were used to generate RNA 5 cDNA clones by RT-PCR on gel-purified RNA 5. Sequencing of these clones and primer extension analysis of transcripts (derived from the cDNA clones) and purified RNA 5 indicated that RNA 5 consists of the conserved 3'-terminal region of genomic RNAs 2 and 3.
对巨细胞病毒Q株(Q-CMV)衣壳化RNA的分析表明,存在一群约300个核苷酸的离散分子,称为RNA 5(佩登,K.W.C.,和西蒙斯,R.H.,《病毒学》53,487 - 492,1973年)。分离出Q-CMV RNA 5,并通过直接RNA测序确定其5'端序列。该序列对应于基因组RNA 1、2和3不完全保守的3'端区域的确切起始位置。由该区域最后130个核苷酸组成的来自RNA 3的探针与RNA 5杂交。含有保守区域5'端和3'端序列的寡核苷酸用于通过对凝胶纯化的RNA 5进行逆转录聚合酶链反应(RT-PCR)来生成RNA 5 cDNA克隆。对这些克隆的测序以及对转录本(源自cDNA克隆)和纯化的RNA 5的引物延伸分析表明,RNA 5由基因组RNA 2和3的保守3'端区域组成。