Literature DB >> 2330672

Sequence characterization of the membrane protein gene of paramyxovirus simian virus 5.

H Sheshberadaran1, R A Lamb.   

Abstract

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.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2330672     DOI: 10.1016/0042-6822(90)90248-p

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  9 in total

1.  Increased readthrough transcription across the simian virus 5 M-F gene junction leads to growth defects and a global inhibition of viral mRNA synthesis.

Authors:  G D Parks; K R Ward; J C Rassa
Journal:  J Virol       Date:  2001-03       Impact factor: 5.103

2.  Characterizations of the human parainfluenza type 2 virus gene encoding the L protein and the intergenic sequences.

Authors:  M Kawano; K Okamoto; H Bando; K Kondo; M Tsurudome; H Komada; M Nishio; Y Ito
Journal:  Nucleic Acids Res       Date:  1991-05-25       Impact factor: 16.971

3.  RNA editing by G-nucleotide insertion in mumps virus P-gene mRNA transcripts.

Authors:  R G Paterson; R A Lamb
Journal:  J Virol       Date:  1990-09       Impact factor: 5.103

4.  Highly diverse intergenic regions of the paramyxovirus simian virus 5 cooperate with the gene end U tract in viral transcription termination and can influence reinitiation at a downstream gene.

Authors:  J C Rassa; G D Parks
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

5.  Flux of the paramyxovirus hemagglutinin-neuraminidase glycoprotein through the endoplasmic reticulum activates transcription of the GRP78-BiP gene.

Authors:  S S Watowich; R I Morimoto; R A Lamb
Journal:  J Virol       Date:  1991-07       Impact factor: 5.103

6.  A novel CD8-independent high-avidity cytotoxic T-lymphocyte response directed against an epitope in the phosphoprotein of the paramyxovirus simian virus 5.

Authors:  P M Gray; G D Parks; M A Alexander-Miller
Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

7.  Molecular evolution of human paramyxoviruses. Nucleotide sequence analyses of the human parainfluenza type 1 virus NP and M protein genes and construction of phylogenetic trees for all the human paramyxoviruses.

Authors:  K Miyahara; S Kitada; M Yoshimoto; H Matsumura; M Kawano; H Komada; M Tsurudome; S Kusagawa; M Nishio; Y Ito
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

8.  Roles for the cytoplasmic tails of the fusion and hemagglutinin-neuraminidase proteins in budding of the paramyxovirus simian virus 5.

Authors:  David L Waning; Anthony P Schmitt; George P Leser; Robert A Lamb
Journal:  J Virol       Date:  2002-09       Impact factor: 5.103

9.  Cloning and sequencing of the matrix protein (M) gene of turkey rhinotracheitis virus reveal a gene order different from that of respiratory syncytial virus.

Authors:  Q Yu; P J Davis; J Li; D Cavanagh
Journal:  Virology       Date:  1992-02       Impact factor: 3.616

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.