Literature DB >> 7906311

Sequence and genome organization of Borna disease virus.

B Cubitt1, C Oldstone, J C de la Torre.   

Abstract

We have previously demonstrated that Borna disease virus (BDV) has a negative nonsegmented single-stranded (NNS) RNA genome that replicates in the nucleus of infected cells. Here we report for the first time the cloning and complete sequence of the BDV genome. Our results revealed that BDV has a genomic organization similar to that of other members of the Mononegavirales order. We have identified five main open reading frames (ORFs). The largest ORF, V, is located closest to the 5' end in the BDV genome and, on the basis of strong homology with other NNS-RNA virus polymerases, is a member of the L-protein family. The intercistronic regions vary in length and nucleotide composition and contain putative transcriptional start and stop signals. BDV untranslated 3' and 5' RNA sequences resemble those of other NNS-RNA viruses. Using a set of overlapping probes across the BDV genome, we identified nine in vivo synthesized species of polyadenylated subgenomic RNAs complementary to the negative-strand RNA genome, including monocistronic transcripts corresponding to ORFs I, II, and IV, as well as six polycistronic polyadenylated BDV RNAs. Interestingly, although ORFs III and V were detected within polycistronic transcripts, their corresponding monocistronic transcripts were not detected. Our data indicate that BDV is a member of the Mononegavirales, specially related to the family Rhabdoviridae. However, in contrast to the rest of the NNS-RNA animal viruses, BDV replication and transcription occur in the nucleus of infected cells. These findings suggest a possible relationship between BDV and the plant rhabdoviruses, which also replicate and transcribe in the nucleus.

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Year:  1994        PMID: 7906311      PMCID: PMC236592     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  61 in total

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2.  A simple and very efficient method for generating cDNA libraries.

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4.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

5.  Replication of Borna disease virus in cell cultures.

Authors:  S Herzog; R Rott
Journal:  Med Microbiol Immunol       Date:  1980       Impact factor: 3.402

6.  In vitro studies on Borna virus. II. Properties of the virus.

Authors:  K Danner; A Mayr
Journal:  Arch Virol       Date:  1979       Impact factor: 2.574

7.  Cloning and DNA sequence of double-stranded copies of haemagglutinin genes from H2 and H3 strains elucidates antigenic shift and drift in human influenza virus.

Authors:  M J Gething; J Bye; J Skehel; M Waterfield
Journal:  Nature       Date:  1980-09-25       Impact factor: 49.962

8.  Polycistronic vesicular stomatitis virus RNA transcripts.

Authors:  R C Herman; M Schubert; J D Keene; R A Lazzarini
Journal:  Proc Natl Acad Sci U S A       Date:  1980-08       Impact factor: 11.205

9.  Detection of antibodies against Borna disease virus in sera and cerebrospinal fluid of horses in the USA.

Authors:  M Kao; A N Hamir; C E Rupprecht; Z F Fu; V Shankar; H Koprowski; B Dietzschold
Journal:  Vet Rec       Date:  1993-03-06       Impact factor: 2.695

10.  Structural and functional characterization of Newcastle disease virus polycistronic RNA species.

Authors:  A Wilde; T Morrison
Journal:  J Virol       Date:  1984-07       Impact factor: 5.103

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  88 in total

1.  Expression and characterization of the Borna disease virus polymerase.

Authors:  M P Walker; I Jordan; T Briese; N Fischer; W I Lipkin
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  Sequence variability of Borna disease virus: resistance to superinfection may contribute to high genome stability in persistently infected cells.

Authors:  S Formella; C Jehle; C Sauder; P Staeheli; M Schwemmle
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

3.  A novel borna disease virus vector system that stably expresses foreign proteins from an intercistronic noncoding region.

Authors:  Takuji Daito; Kan Fujino; Tomoyuki Honda; Yusuke Matsumoto; Yohei Watanabe; Keizo Tomonaga
Journal:  J Virol       Date:  2011-09-21       Impact factor: 5.103

4.  Implication of a cis-acting element in the cytoplasmic accumulation of unspliced Borna disease virus RNAs.

Authors:  P A Schneider; M Schwemmle; W I Lipkin
Journal:  J Virol       Date:  1997-11       Impact factor: 5.103

Review 5.  Borna disease virus and human disease.

Authors:  K M Carbone
Journal:  Clin Microbiol Rev       Date:  2001-07       Impact factor: 26.132

6.  A methionine-rich domain mediates CRM1-dependent nuclear export activity of Borna disease virus phosphoprotein.

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Journal:  J Virol       Date:  2006-02       Impact factor: 5.103

7.  RNA splicing in Borna disease virus, a nonsegmented, negative-strand RNA virus.

Authors:  P A Schneider; A Schneemann; W I Lipkin
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

8.  Developmental alterations in serotoninergic neurotransmission in Borna disease virus (BDV)-infected rats: a multidisciplinary analysis.

Authors:  David Dietz; Michael Vogel; Steven Rubin; Timothy Moran; Kathryn Carbone; Mikhail Pletnikov
Journal:  J Neurovirol       Date:  2004-10       Impact factor: 2.643

9.  Borna disease virus (BDV), a nonsegmented RNA virus, replicates in the nuclei of infected cells where infectious BDV ribonucleoproteins are present.

Authors:  B Cubitt; J C de la Torre
Journal:  J Virol       Date:  1994-03       Impact factor: 5.103

10.  Persistence of Borna disease virus in naturally infected sheep.

Authors:  Thomas W Vahlenkamp; Andrea Konrath; Matthias Weber; Hermann Müller
Journal:  J Virol       Date:  2002-10       Impact factor: 5.103

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