Literature DB >> 7831839

The termini of VSV DI particle RNAs are sufficient to signal RNA encapsidation, replication, and budding to generate infectious particles.

A K Pattnaik1, L A Ball, A LeGrone, G W Wertz.   

Abstract

Infectious defective interfering (DI) particles of the negative-stranded RNA virus vesicular stomatitis virus (VSV) have been recovered from negative-sense transcripts of a plasmid that contains a full-length cDNA derived from the DI-T particle genome. In order to determine the cis-acting sequences necessary for RNA replication, encapsidation, and budding and to approximate the minimal size of RNA that can be packaged into infectious particles, we constructed a series of internal deletions in the DI cDNA to generate plasmids that could be transcribed to yield RNAs which ranged in size from 2209 nucleotides down to 102 nucleotides. All the deletion plasmids retained at least 36 nucleotides from the 5'-terminus and 51 nucleotides from the 3'-terminus of the DI genome. In cells expressing the five VSV proteins, the deleted DI RNAs were examined for their ability to be encapsidated, to replicate, and to bud to produce infectious DI particles. An RNA as small as 191 nucleotides, which contained 46 nucleotides from the 5'-end and 145 nucleotides from the 3'-end of the DI genome was encapsidated, replicated, and budded at least as efficiently as the full-length wild-type DI RNA. In contrast, a 102-nucleotide RNA that contained only the 51 nucleotides from the 5'-end of the DI RNA and its perfect 51-nucleotide complement at the 3'-end replicated poorly and failed to bud infectious DI particles. However, an RNA with an insertion of 1499-nucleotide "stuffer" sequences of non-VSV origin between the two 51-nucleotide complementary termini not only replicated but also budded infectious particles. These data show that the signals necessary for RNA encapsidation, replication, and packaging into infectious DI particles are contained within the 5'-terminal 36 nucleotides and the 3'-terminal 51 nucleotides of the DI RNA genome. Furthermore, the results show that a heterologous sequence can be replicated and packaged into infectious particles if it is flanked by the DI RNA termini.

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Year:  1995        PMID: 7831839      PMCID: PMC7131126          DOI: 10.1016/s0042-6822(95)80005-0

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


  33 in total

1.  Characterization of an internal element in turnip crinkle virus RNA involved in both coat protein binding and replication.

Authors:  N Wei; D L Hacker; T J Morris
Journal:  Virology       Date:  1992-09       Impact factor: 3.616

2.  Deletion mapping of Sindbis virus DI RNAs derived from cDNAs defines the sequences essential for replication and packaging.

Authors:  R Levis; B G Weiss; M Tsiang; H Huang; S Schlesinger
Journal:  Cell       Date:  1986-01-17       Impact factor: 41.582

3.  Rescue of synthetic analogs of genomic RNA and replicative-intermediate RNA of human parainfluenza virus type 3.

Authors:  K Dimock; P L Collins
Journal:  J Virol       Date:  1993-05       Impact factor: 5.103

Review 4.  The origins of defective interfering particles of the negative-strand RNA viruses.

Authors:  R A Lazzarini; J D Keene; M Schubert
Journal:  Cell       Date:  1981-10       Impact factor: 41.582

5.  Replication and amplification of defective interfering particle RNAs of vesicular stomatitis virus in cells expressing viral proteins from vectors containing cloned cDNAs.

Authors:  A K Pattnaik; G W Wertz
Journal:  J Virol       Date:  1990-06       Impact factor: 5.103

6.  cis-acting requirements for the replication of flock house virus RNA 2.

Authors:  L A Ball; Y Li
Journal:  J Virol       Date:  1993-06       Impact factor: 5.103

7.  Assembly and transcription of synthetic vesicular stomatitis virus nucleocapsids.

Authors:  S A Moyer; S Smallwood-Kentro; A Haddad; L Prevec
Journal:  J Virol       Date:  1991-05       Impact factor: 5.103

8.  N protein alone satisfies the requirement for protein synthesis during RNA replication of vesicular stomatitis virus.

Authors:  J T Patton; N L Davis; G W Wertz
Journal:  J Virol       Date:  1984-02       Impact factor: 5.103

9.  Infectious defective interfering particles of VSV from transcripts of a cDNA clone.

Authors:  A K Pattnaik; L A Ball; A W LeGrone; G W Wertz
Journal:  Cell       Date:  1992-06-12       Impact factor: 41.582

10.  Structure and origin of a snapback defective interfering particle RNA of vesicular stomatitis virus.

Authors:  M Schubert; R A Lazzarini
Journal:  J Virol       Date:  1981-02       Impact factor: 5.103

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  38 in total

1.  "Rule of six": how does the Sendai virus RNA polymerase keep count?

Authors:  D Vulliémoz; L Roux
Journal:  J Virol       Date:  2001-05       Impact factor: 5.103

2.  Transcription and replication initiate at separate sites on the vesicular stomatitis virus genome.

Authors:  Sean P J Whelan; Gail W Wertz
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-27       Impact factor: 11.205

3.  Chemical modification of nucleotide bases and mRNA editing depend on hexamer or nucleoprotein phase in Sendai virus nucleocapsids.

Authors:  Frédéric Iseni; Florence Baudin; Dominique Garcin; Jean-Baptiste Marq; Rob W H Ruigrok; Daniel Kolakofsky
Journal:  RNA       Date:  2002-08       Impact factor: 4.942

4.  Utilization of homotypic and heterotypic proteins of vesicular stomatitis virus by defective interfering particle genomes for RNA replication and virion assembly: implications for the mechanism of homologous viral interference.

Authors:  Gyoung Nyoun Kim; C Yong Kang
Journal:  J Virol       Date:  2005-08       Impact factor: 5.103

5.  Evidence that the respiratory syncytial virus polymerase is recruited to nucleotides 1 to 11 at the 3' end of the nucleocapsid and can scan to access internal signals.

Authors:  Vanessa M Cowton; Rachel Fearns
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

6.  Ambisense gene expression from recombinant rabies virus: random packaging of positive- and negative-strand ribonucleoprotein complexes into rabies virions.

Authors:  S Finke; K K Conzelmann
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

7.  Secondary structure determination of the conserved 98-base sequence at the 3' terminus of hepatitis C virus genome RNA.

Authors:  K J Blight; C M Rice
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

8.  Deletion analysis of a defective interfering Semliki Forest virus RNA genome defines a region in the nsP2 sequence that is required for efficient packaging of the genome into virus particles.

Authors:  C L White; M Thomson; N J Dimmock
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

9.  Importance of hydrogen bond contacts between the N protein and RNA genome of vesicular stomatitis virus in encapsidation and RNA synthesis.

Authors:  Edward W Rainsford; Djamila Harouaka; Gail W Wertz
Journal:  J Virol       Date:  2009-12-09       Impact factor: 5.103

10.  Identification of a highly conserved sequence element at the 3' terminus of hepatitis C virus genome RNA.

Authors:  A A Kolykhalov; S M Feinstone; C M Rice
Journal:  J Virol       Date:  1996-06       Impact factor: 5.103

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