SEQUENCE CHARACTERIZATION OF THE MEMBRANE-PROTEIN GENE OF PARAMYXOVIRUS SIMIAN VIRUS-5

被引:29
作者
SHESHBERADARAN, H [1 ]
LAMB, RA [1 ]
机构
[1] NORTHWESTERN UNIV,DEPT BIOCHEM MOLEC BIOL & CELL BIOL,EVANSTON,IL 60208
关键词
D O I
10.1016/0042-6822(90)90248-P
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The complete nucleotide sequence of the membrane (M) protein gene of the paramyxovirus simian virus 5 (SV5) was determined from cDNA clones of viral mRNAs. The M gene boundaries were determined by (i) primer extension sequencing on M mRNA; (ii) nuclease S1 analysis; and (iii) primer extension sequencing on viral genomic RNA. The M gene mRNA consisted of 1371 templated nucleotides. It contains a single large open reading frame that can encode a protein of 377 amino acids with a predicted Mr = 42,253. The authenticity of the predicted M protein coding sequence was confirmed by synthesis of the M protein from mRNA synthesized from cDNA. The predicted M amino acid sequence indicated it is an overall hydrophobic protein carrying a net positive charge. Alignment of the SV5 protein amino acid sequence with the M protein sequences of other paramyxoviruses indicated that these viruses fall into the following two groups: (1) SV5, mumps virus, and Newcastle disease virus; or (2) Sendai, parainfluenza virus type 3, measles virus, and canine distemper virus, with mumps virus M sequence being the most closely related to SV5. © 1990.
引用
收藏
页码:234 / 243
页数:10
相关论文
共 51 条
[31]   ANALYSIS AND GENE ASSIGNMENT OF MESSENGER-RNAS OF A PARAMYXOVIRUS, SIMIAN VIRUS-5 [J].
PATERSON, RG ;
HARRIS, TJR ;
LAMB, RA .
VIROLOGY, 1984, 138 (02) :310-323
[32]   FUSION PROTEIN OF THE PARAMYXOVIRUS SIMIAN-VIRUS 5 - NUCLEOTIDE-SEQUENCE OF MESSENGER-RNA PREDICTS A HIGHLY HYDROPHOBIC GLYCOPROTEIN [J].
PATERSON, RG ;
HARRIS, TJR ;
LAMB, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (21) :6706-6710
[33]   EXPRESSION AT THE CELL-SURFACE OF BIOLOGICALLY-ACTIVE FUSION AND HEMAGGLUTININ NEURAMINIDASE PROTEINS OF THE PARAMYXOVIRUS SIMIAN VIRUS-5 FROM CLONED CDNA [J].
PATERSON, RG ;
HIEBERT, SW ;
LAMB, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (22) :7520-7524
[34]   MUTATION IN THE MATRIX PROTEIN OF NEWCASTLE-DISEASE VIRUS CAN RESULT IN DECREASED FUSION GLYCOPROTEIN INCORPORATION INTO PARTICLES AND DECREASED INFECTIVITY [J].
PEEPLES, ME ;
BRATT, MA .
JOURNAL OF VIROLOGY, 1984, 51 (01) :81-90
[35]   POLYPEPTIDE-SYNTHESIS IN SIMIAN VIRUS-5-INFECTED CELLS [J].
PELUSO, RW ;
LAMB, RA ;
CHOPPIN, PW .
JOURNAL OF VIROLOGY, 1977, 23 (01) :177-187
[36]   A COMPREHENSIVE SEQUENCE-ANALYSIS PROGRAM FOR THE IBM PERSONAL-COMPUTER [J].
QUEEN, C ;
KORN, LJ .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :581-599
[37]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[38]  
SATO H, 1987, VIRUS RES, V7, P241
[39]  
SATO H, 1987, VIRUS RES, V8, P217, DOI 10.1016/0168-1702(87)90017-7
[40]   IDENTIFICATION OF BIOLOGICAL-ACTIVITIES OF PARAMYXOVIRUS GLYCOPROTEINS - ACTIVATION OF CELL-FUSION, HEMOLYSIS, AND INFECTIVITY BY PROTEOLYTIC CLEAVAGE OF AN INACTIVE PRECURSOR PROTEIN OF SENDAI VIRUS [J].
SCHEID, A ;
CHOPPIN, PW .
VIROLOGY, 1974, 57 (02) :475-490