Literature DB >> 6168769

Small reovirus particle composed solely of sigma NS with specificity for binding different nucleic acids.

P J Gomatos, O Prakash, N M Stamatos.   

Abstract

We reported previously that polycytidylate [poly(C)]-dependent RNA polymerase activity was a property of small spherical or triangular reovirus-specific particles which sedimented at 13 to 19S and were composed solely of the reovirus protein, sigma NS. Depending on the fraction of cellular extracts from which they were obtained, these particles exhibited marked differences in stability. Most 13 to 19S particles from a particular fraction repeatedly disaggregated into smaller 4 to 5S subunits with no enzymatic activity. Disruption of many particles could be prevented and polymerase activity retained after these particles had bound different single-stranded (ss) RNAs. Our previous results indicated that there was heterogeneity among the 13 to 19S particles in that possession of poly(C)-dependent RNA polymerase activity was a property of only some. Support for this heterogeneity was derived from the demonstration in this report that there were at least three types of binding sites present within particles in any purified preparation: (i) those binding only poly(C); (ii) those binding only reovirus ss RNAs; and (iii) those binding one or the other, but not both at the same time. It is suggested that only those particles able to bind either poly(C) or reovirus ss RNAs had poly(C)-dependent RNA polymerase activity, as reovirus ss RNAs markedly inhibited the polymerase activity. All three size classes of reovirus ss RNAs were equally effective in binding, but once bound, they were not copied. It is possible that heterogeneity in binding capacity of different particles comprised of only one protein, sigma NS, could result from the ability of subunits containing this protein to assemble into slightly different 13 to 19S particles with specificity of binding or polymerase activity conferred by the configuration of the assembled particles. The high capacity of sigma NS to bind many different nucleic acids with some specificity suggests that these particles may act during infection as condensing agents to bring together 10 reovirus ss RNA templates in preparation for double-stranded RNA synthesis.

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Year:  1981        PMID: 6168769      PMCID: PMC171271          DOI: 10.1128/JVI.39.1.115-124.1981

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


  15 in total

1.  Synthesis of reovirus-specific polypeptides in cells pretreated with cycloheximide.

Authors:  R Y Lau; D Van Alstyne; R Berckmans; A F Graham
Journal:  J Virol       Date:  1975-09       Impact factor: 5.103

2.  Reovirus-coded polypeptides in infected cells: isolation of two native monomeric polypeptides with affinity for single-stranded and double-stranded RNA, respectively.

Authors:  H Huismans; W K Joklik
Journal:  Virology       Date:  1976-04       Impact factor: 3.616

3.  Reovirus-specific enzyme(s) associated with subviral particles responds in vitro to polyribocytidylate to yield double-stranded polyribocytidylate-polyriboguanylate.

Authors:  P J Gomatos; I Kuechenthal
Journal:  J Virol       Date:  1977-07       Impact factor: 5.103

4.  Temperature-sensitive mutants of reovirus type 3: defects in viral maturation as studied by immunofluorescence and electron microscopy.

Authors:  B N Fields; C S Raine; S G Baum
Journal:  Virology       Date:  1971-03       Impact factor: 3.616

5.  Temperature-sensitive mutants of reovirus. I. Patterns of gene expression by mutants of groups C, D, and E.

Authors:  Y Ito; W K Joklik
Journal:  Virology       Date:  1972-10       Impact factor: 3.616

6.  The nature of the polypeptide encoded by each of the 10 double-stranded RNA segments of reovirus type 3.

Authors:  M A McCrae; W K Joklik
Journal:  Virology       Date:  1978-09       Impact factor: 3.616

7.  A genetic map of reovirus. II. Assignment of the double-stranded RNA-negative mutant groups C, D, and E to genome segments.

Authors:  R F Ramig; T A Mustoe; A H Sharpe; B N Fields
Journal:  Virology       Date:  1978-04       Impact factor: 3.616

8.  Synthesis of all the gene products of the reovirus genome in vivo and in vitro.

Authors:  G W Both; S Lavi; A J Shatkin
Journal:  Cell       Date:  1975-02       Impact factor: 41.582

9.  Nonpermissive infection of L cells by an avian reovirus: restricted transcription of the viral genome.

Authors:  D A Spandidos; A F Graham
Journal:  J Virol       Date:  1976-09       Impact factor: 5.103

10.  Reovirus-specific, single-stranded RNA's synthesized in vitro with enzyme purified from reovirus-infected cells.

Authors:  P J Gomatos
Journal:  J Mol Biol       Date:  1968-11-14       Impact factor: 5.469

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  16 in total

1.  Reovirus sigma NS protein localizes to inclusions through an association requiring the mu NS amino terminus.

Authors:  Cathy L Miller; Teresa J Broering; John S L Parker; Michelle M Arnold; Max L Nibert
Journal:  J Virol       Date:  2003-04       Impact factor: 5.103

2.  Reovirus nonstructural protein mu NS recruits viral core surface proteins and entering core particles to factory-like inclusions.

Authors:  Teresa J Broering; Jonghwa Kim; Cathy L Miller; Caroline D S Piggott; Jason B Dinoso; Max L Nibert; John S L Parker
Journal:  J Virol       Date:  2004-02       Impact factor: 5.103

3.  Proteolytic cleavage of the reovirus sigma 3 protein results in enhanced double-stranded RNA-binding activity: identification of a repeated basic amino acid motif within the C-terminal binding region.

Authors:  J E Miller; C E Samuel
Journal:  J Virol       Date:  1992-09       Impact factor: 5.103

4.  Gene-specific inhibition of reovirus replication by RNA interference.

Authors:  Takeshi Kobayashi; James D Chappell; Pranav Danthi; Terence S Dermody
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

5.  In vitro phosphorylation and purification of a nonstructural protein of bluetongue virus with affinity for single-stranded RNA.

Authors:  H Huismans; A A van Dijk; A R Bauskin
Journal:  J Virol       Date:  1987-11       Impact factor: 5.103

6.  Reovirus sigmaNS protein is required for nucleation of viral assembly complexes and formation of viral inclusions.

Authors:  M M Becker; M I Goral; P R Hazelton; G S Baer; S E Rodgers; E G Brown; K M Coombs; T S Dermody
Journal:  J Virol       Date:  2001-02       Impact factor: 5.103

Review 7.  The biochemistry of orbiviruses. Brief review.

Authors:  R P Spence; N F Moore; P A Nuttall
Journal:  Arch Virol       Date:  1984       Impact factor: 2.574

8.  Binding to selected regions of reovirus mRNAs by a nonstructural reovirus protein.

Authors:  N M Stamatos; P J Gomatos
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

9.  Identification of the RNA-binding, dimerization, and eIF4GI-binding domains of rotavirus nonstructural protein NSP3.

Authors:  M Piron; T Delaunay; J Grosclaude; D Poncet
Journal:  J Virol       Date:  1999-07       Impact factor: 5.103

10.  Reovirus Nonstructural Protein σNS Acts as an RNA Stability Factor Promoting Viral Genome Replication.

Authors:  Paula F Zamora; Liya Hu; Jonathan J Knowlton; Roni M Lahr; Rodolfo A Moreno; Andrea J Berman; B V Venkataram Prasad; Terence S Dermody
Journal:  J Virol       Date:  2018-07-17       Impact factor: 5.103

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