Sato H, Oh-hira M, Ishida N, Imamura Y, Hattori S, Kawakita M
Virus Res. 1987 May;7(3):241-55. doi: 10.1016/0168-1702(87)90031-1.
Molecular cloning of most if not all of the genome of an avirulent strain D26 of Newcastle disease virus (NDV) was carried out. cDNA clones were aligned by mutual hybridization and restriction map analysis. The nucleotide sequence of 3672 bases which completed the partial sequence of P gene reported in our previous paper (Ishida, N. et al., 1986, Nucleic Acids Res. 14, 6551-6564), and also covered M and F genes, was determined. Each gene contained one long open reading frame which could code for polypeptides of 395, 364, and 553 amino acid residues, respectively. The deduced amino acid sequences of P and M gene products showed little homology to those of other paramyxoviruses. In contrast, comparison of the amino acid sequence of the F gene product revealed highly conserved regions including the amino terminal sequence of the F1 portion following the putative processing site. There was only one basic amino acid residue at the putative processing site, which would explain the low virulence of this strain.
对新城疫病毒(NDV)无毒力毒株D26的大部分(如果不是全部)基因组进行了分子克隆。通过相互杂交和限制性图谱分析对cDNA克隆进行比对。测定了3672个碱基的核苷酸序列,该序列完成了我们之前论文(Ishida, N.等人,1986年,《核酸研究》14卷,6551 - 6564页)中报道的P基因部分序列,并且还涵盖了M和F基因。每个基因都包含一个长开放阅读框,分别可编码395、364和553个氨基酸残基的多肽。P和M基因产物的推导氨基酸序列与其他副粘病毒的序列几乎没有同源性。相比之下,F基因产物氨基酸序列的比较显示出高度保守的区域,包括假定加工位点之后F1部分的氨基末端序列。在假定加工位点只有一个碱性氨基酸残基,这可以解释该毒株的低毒力。