Kondo K, Bando H, Tsurudome M, Kawano M, Nishio M, Ito Y
Department of Microbiology, Mie University School of Medicine, Tokyo, Japan.
Virology. 1990 Sep;178(1):321-6. doi: 10.1016/0042-6822(90)90413-l.
We cloned and sequenced the cDNAs against genomic RNAs and mRNAs for phosphoproteins (Ps) of human parainfluenza virus types 4A (PIV-4A) and 4B (PIV-4B). The PIV-4A and -4B P genes were 1535 nucleotides including poly(A) tract and were found to have two small open reading frames, neither of which was apparently large enough to encode the P protein. A cluster of G residues was found in genomic RNA and the number of G residues was 6 in both PIV-4A and -4B. However, the number of G residues at the corresponding site in the mRNAs to the genomic RNA was not constant. Three different mRNA cDNA clones were obtained; the first type of mRNA encodes a larger (P) protein of 399 amino acids, the second type encodes V protein of 229 or 230 amino acids, and the third type encodes the smallest protein (156 amino acids). Comparisons on the nucleotide and the amino acid sequences P and V proteins between these two subtypes revealed extensive homologies. However, these homology degrees are lower than that of NP protein. The C-terminal regions of the P and V proteins of PIV-4s could be aligned with all other Paramyxoviruses, PIV-2, mumps virus (MuV), simian virus 5 (SV 5), Newcastle disease virus (NDV), measles virus (MV), canine distemper virus (CDV), Sendai virus (SV), and PIV-3. On the other hand, the P-V common (N-terminal) regions showed no homology with MV, CDV, SV, and PIV-3. Seven phylogenetic trees of Paramyxoviruses were constructed from the entire and partial regions of P and V proteins.
我们针对人副流感病毒4型A(PIV - 4A)和4型B(PIV - 4B)的磷蛋白(Ps),克隆了基因组RNA和mRNA的cDNA并进行测序。PIV - 4A和 - 4B的P基因包含多聚腺苷酸尾,长度为1535个核苷酸,发现有两个小的开放阅读框,但显然都不足以编码P蛋白。在基因组RNA中发现了一串鸟嘌呤(G)残基,PIV - 4A和 - 4B中的G残基数均为6个。然而,与基因组RNA相对应的mRNA中该位点的G残基数并不恒定。获得了三种不同的mRNA cDNA克隆;第一种类型的mRNA编码一个由399个氨基酸组成的较大(P)蛋白,第二种类型编码由229或230个氨基酸组成的V蛋白,第三种类型编码最小的蛋白(156个氨基酸)。对这两个亚型的P和V蛋白的核苷酸和氨基酸序列进行比较,发现有广泛的同源性。然而,这些同源程度低于核蛋白(NP)。PIV - 4的P和V蛋白的C末端区域可以与所有其他副粘病毒、PIV - 2、腮腺炎病毒(MuV)、猴病毒5(SV 5)、新城疫病毒(NDV)、麻疹病毒(MV)、犬瘟热病毒(CDV)、仙台病毒(SV)和PIV - 3对齐。另一方面,P - V共同(N末端)区域与MV、CDV、SV和PIV - 3没有同源性。根据P和V蛋白的全部和部分区域构建了七个副粘病毒的系统发育树。