SEQUENCE-ANALYSIS OF THE PHOSPHOPROTEIN-(P) GENES OF HUMAN PARAINFLUENZA TYPE-4A AND TYPE-4B VIRUSES AND RNA EDITING AT TRANSCRIPT OF THE P-GENES - THE NUMBER OF G RESIDUES ADDED IS IMPRECISE

被引:59
作者
KONDO, K
BANDO, H
TSURUDOME, M
KAWANO, M
NISHIO, M
ITO, Y
机构
[1] MIE UNIV,SCH MED,DEPT MICROBIOL,2-174 EDOBASH,TSU,MIE 514,JAPAN
[2] FUJIKURA KASEI CO LTD,FUJIKURA RES CTR,ITABASHI KU,TOKYO 174,JAPAN
关键词
D O I
10.1016/0042-6822(90)90413-L
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 of 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. © 1990.
引用
收藏
页码:321 / 326
页数:6
相关论文
共 23 条
  • [1] MOLECULAR-CLONING AND SEQUENCE-ANALYSIS OF HUMAN PARAINFLUENZA TYPE-4A VIRUS HN GENE - ITS IRREGULARITIES ON STRUCTURE AND ACTIVITIES
    BANDO, H
    KONDO, K
    KAWANO, M
    KOMADA, H
    TSURUDOME, M
    NISHIO, M
    ITO, Y
    [J]. VIROLOGY, 1990, 175 (01) : 307 - 312
  • [2] NUCLEOTIDE-SEQUENCE OF THE ENTIRE PROTEIN CODING REGION OF CANINE-DISTEMPER VIRUS POLYMERASE-ASSOCIATED (P) PROTEIN MESSENGER-RNA
    BARRETT, T
    SHRIMPTON, SB
    RUSSELL, SEH
    [J]. VIRUS RESEARCH, 1985, 3 (04) : 367 - 372
  • [3] MEASLES VIRUS-P GENE CODES FOR 2 PROTEINS
    BELLINI, WJ
    ENGLUND, G
    ROZENBLATT, S
    ARNHEITER, H
    RICHARDSON, CD
    [J]. JOURNAL OF VIROLOGY, 1985, 53 (03) : 908 - 919
  • [4] ANTIGENIC VARIATION AMONG NEWLY ISOLATED STRAINS OF PARAINFLUENZA TYPE 4 VIRUS
    CANCHOLA, J
    CHRISTMANN, E
    KIM, HW
    PARROTT, RH
    CHANOCK, RM
    VARGOSKO, AJ
    JEFFRIES, B
    [J]. AMERICAN JOURNAL OF HYGIENE, 1964, 79 (03): : 357 - &
  • [5] MUTATED AND HYPERMUTATED GENES OF PERSISTENT MEASLES VIRUSES WHICH CAUSED LETHAL HUMAN-BRAIN DISEASES
    CATTANEO, R
    SCHMID, A
    SPIELHOFER, P
    KAELIN, K
    BACZKO, K
    TERMEULEN, V
    PARDOWITZ, J
    FLANAGAN, S
    RIMA, BK
    UDEM, SA
    BILLETER, MA
    [J]. VIROLOGY, 1989, 173 (02) : 415 - 425
  • [6] MEASLES-VIRUS EDITING PROVIDES AN ADDITIONAL CYSTEINE-RICH PROTEIN
    CATTANEO, R
    KAELIN, K
    BACZKO, K
    BILLETER, MA
    [J]. CELL, 1989, 56 (05) : 759 - 764
  • [7] CHANOCK RM, 1985, VIROLOGY, P1241
  • [8] NH2-TERMINAL ACIDIC REGION OF THE PHOSPHOPROTEIN OF VESICULAR STOMATITIS-VIRUS CAN BE FUNCTIONALLY REPLACED BY TUBULIN
    CHATTOPADHYAY, D
    BANERJEE, AK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) : 7977 - 7981
  • [9] SENDAI VIRUS CONTAINS OVERLAPPING GENES EXPRESSED FROM A SINGLE MESSENGER-RNA
    GIORGI, C
    BLUMBERG, BM
    KOLAKOFSKY, D
    [J]. CELL, 1983, 35 (03) : 829 - 836
  • [10] Kimura M., 1983, NEUTRAL THEORY MOL E