Literature DB >> 6991125

Yeast viral double-stranded RNAs have heterogeneous 3' termini.

J A Bruenn, V E Brennan.   

Abstract

The yeast virus, ScV, is communicated only by mating. It has two separately encapsidated dsRNAs. One of these, L, codes for the major capsid polypeptide. The other, M, codes for a polypeptide toxic to yeasts without ScV-M particles. Defective interfering particles containing fragments of M (S) displace ScV-M when they arise. We have shown that five independently isolated S dsRNAs are all derived by internal deletion of M. The 3' ends of all the ScV dsRNAs are markedly heterogeneous. For instance, half of the first 35 nucleotides at one 3' end of M and S are variable. Conserved sequences at the 3' ends of M and S are AAACACCCAUCAOH and AUUUCUUUAUUUUUCAOH. Conserved sequences at the 3' ends of L are UAAAAAUUUUUCAOH and AAAAAUXCAOH, where X is variable. We propose that the sequence AUUUUUCAOH is a recognition sequence for the capsid-associated single-stranded RNA polymerase activity. Since all the viral RNAs have pppGp 5' termini, their 3' termini probably extended one nucleotide beyond the terminal pppGp.

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Year:  1980        PMID: 6991125     DOI: 10.1016/0092-8674(80)90084-7

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  34 in total

1.  Yeast L double-stranded ribonucleic acid is synthesized during the G1 phase but not the S phase of the cell cycle.

Authors:  V A Zakian; D W Wagner; W L Fangman
Journal:  Mol Cell Biol       Date:  1981-08       Impact factor: 4.272

2.  Both yeast W double-stranded RNA and its single-stranded form 20S RNA are linear.

Authors:  N Rodriguez-Cousiño; R Esteban
Journal:  Nucleic Acids Res       Date:  1992-06-11       Impact factor: 16.971

3.  Defective Interference in the Killer System of Saccharomyces cerevisiae.

Authors:  S P Ridley; R B Wickner
Journal:  J Virol       Date:  1983-02       Impact factor: 5.103

4.  Structural properties of double-stranded RNAs associated with biological control of chestnut blight fungus.

Authors:  J Tartaglia; C P Paul; D W Fulbright; D L Nuss
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

5.  Nontemplated terminal nucleotidyltransferase activity of double-stranded RNA bacteriophage phi6 RNA-dependent RNA polymerase.

Authors:  Minna M Poranen; Minni R L Koivunen; Dennis H Bamford
Journal:  J Virol       Date:  2008-07-09       Impact factor: 5.103

6.  Two biochemically and genetically different forms of L dsRNA of Saccharomyces cerevisiae exist: One form, L2, is correlated.

Authors:  M El-Sherbeini; E A Bevan; D J Mitchell
Journal:  Curr Genet       Date:  1983-03       Impact factor: 3.886

7.  In vivo mapping of a sequence required for interference with the yeast killer virus.

Authors:  B F Huan; Y Q Shen; J A Bruenn
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-15       Impact factor: 11.205

8.  Co-curing of plasmids affecting killer double-stranded RNAs of Saccharomyces cerevisiae: [HOK], [NEX], and the abundance of L are related and further evidence that M1 requires L.

Authors:  S S Sommer; R B Wickner
Journal:  J Bacteriol       Date:  1982-05       Impact factor: 3.490

9.  Separation and sequence of the 3' termini of M double-stranded RNA from killer yeast.

Authors:  D J Thiele; R W Wang; M J Leibowitz
Journal:  Nucleic Acids Res       Date:  1982-03-11       Impact factor: 16.971

10.  Overlapping genes in a yeast double-stranded RNA virus.

Authors:  M E Diamond; J J Dowhanick; M E Nemeroff; D F Pietras; C L Tu; J A Bruenn
Journal:  J Virol       Date:  1989-09       Impact factor: 5.103

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