Steward M, Vipond I B, Millar N S, Emmerson P T
Department of Biochemistry and Genetics, Medical School, University of Newcastle upon Tyne, U.K.
J Gen Virol. 1993 Dec;74 ( Pt 12):2539-47. doi: 10.1099/0022-1317-74-12-2539.
The co-transcriptional editing of the Newcastle disease virus (NDV) P gene has been studied by sequence analysis of cloned viral genomic RNA and mRNA. Evidence has been obtained for the specific insertion of non-templated G nucleotides, the consequence of which is the generation of three populations of P gene-derived mRNAs. The three populations encode proteins (P, V and W) which have a common N-terminal region, but which utilize three different reading frames at their C termini. Paradoxically, NDV edits its P gene mRNA by the insertion of non-templated G residues in a manner similar to Sendai and measles viruses (P-->V editing) despite its apparent closer evolutionary relationship to the simian virus type 5, mumps and related group of viruses which edit a V genomic sequence to generate an mRNA to encode a functional P protein (V-->P editing).
通过对克隆的病毒基因组RNA和mRNA进行序列分析,研究了新城疫病毒(NDV)P基因的共转录编辑。已获得非模板化G核苷酸特异性插入的证据,其结果是产生了三种源自P基因的mRNA群体。这三种群体编码的蛋白质(P、V和W)具有共同的N端区域,但在其C端利用三种不同的阅读框。矛盾的是,尽管新城疫病毒与猿猴病毒5型、腮腺炎病毒及相关病毒组在进化上明显更接近,后者通过编辑V基因组序列来产生编码功能性P蛋白的mRNA(V→P编辑),但新城疫病毒仍以类似于仙台病毒和麻疹病毒的方式(P→V编辑)通过插入非模板化G残基来编辑其P基因mRNA。