Ishida N, Taira H, Omata T, Mizumoto K, Hattori S, Iwasaki K, Kawakita M
Nucleic Acids Res. 1986 Aug 26;14(16):6551-64. doi: 10.1093/nar/14.16.6551.
DNA fragments complementary to the Newcastle disease virus genome (strain D26) were cloned and sequenced. The sequence of 2,617 nucleotides from the 3' end of the genome was determined and an open reading frame (OP-1) consisting of 1,467 nucleotides, most likely encoding NP protein, was found in this region. This was followed by a second unfinished open reading frame (OP-2) of at least 729 nucleotides which continued beyond the 2,617th nucleotide. Another relatively short (312 nucleotides long) open reading frame (OP-2') was found overlapping with OP-2, but its significance is still unclear. The amino acid sequence deduced from the nucleotide sequence of OP-1 showed a moderate homology to that of the NP protein of Sendai virus in the central portion of the peptide. The leader sequence of 53 nucleotides was also identified. The 5' end of mRNAs synthesized in the infected cells was analyzed and found to be m7GpppA, suggesting that the transcription of viral mRNAs starts with A, but not with G residue.
克隆并测序了与新城疫病毒基因组(D26株)互补的DNA片段。测定了基因组3'端2617个核苷酸的序列,在此区域发现了一个由1467个核苷酸组成的开放阅读框(OP-1),最有可能编码NP蛋白。紧随其后的是第二个未完成的开放阅读框(OP-2),至少有729个核苷酸,其长度超过了第2617个核苷酸。还发现了另一个相对较短(312个核苷酸长)的开放阅读框(OP-2')与OP-2重叠,但其意义仍不清楚。从OP-1的核苷酸序列推导的氨基酸序列在肽的中部与仙台病毒NP蛋白的氨基酸序列有适度的同源性。还鉴定出了53个核苷酸的前导序列。对感染细胞中合成的mRNA的5'端进行了分析,发现是m7GpppA,这表明病毒mRNA的转录起始于A,而不是G残基。