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. 1996 Mar;60(1):250–265. doi: 10.1128/mr.60.1.250-265.1996

Double-stranded RNA viruses of Saccharomyces cerevisiae.

R B Wickner 1
PMCID: PMC239427  PMID: 8852903

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Selected References

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  1. Atkins J. F., Weiss R. B., Thompson S., Gesteland R. F. Towards a genetic dissection of the basis of triplet decoding, and its natural subversion: programmed reading frame shifts and hops. Annu Rev Genet. 1991;25:201–228. doi: 10.1146/annurev.ge.25.120191.001221. [DOI] [PubMed] [Google Scholar]
  2. Balasundaram D., Dinman J. D., Wickner R. B., Tabor C. W., Tabor H. Spermidine deficiency increases +1 ribosomal frameshifting efficiency and inhibits Ty1 retrotransposition in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1994 Jan 4;91(1):172–176. doi: 10.1073/pnas.91.1.172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ball S. G., Tirtiaux C., Wickner R. B. Genetic Control of L-a and L-(Bc) Dsrna Copy Number in Killer Systems of SACCHAROMYCES CEREVISIAE. Genetics. 1984 Jun;107(2):199–217. doi: 10.1093/genetics/107.2.199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Belcourt M. F., Farabaugh P. J. Ribosomal frameshifting in the yeast retrotransposon Ty: tRNAs induce slippage on a 7 nucleotide minimal site. Cell. 1990 Jul 27;62(2):339–352. doi: 10.1016/0092-8674(90)90371-K. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Belfort M., Perlman P. S. Mechanisms of intron mobility. J Biol Chem. 1995 Dec 22;270(51):30237–30240. doi: 10.1074/jbc.270.51.30237. [DOI] [PubMed] [Google Scholar]
  6. Bevan E. A., Herring A. J., Mitchell D. J. Preliminary characterization of two species of dsRNA in yeast and their relationship to the "killer" character. Nature. 1973 Sep 14;245(5420):81–86. doi: 10.1038/245081b0. [DOI] [PubMed] [Google Scholar]
  7. Bishop D. H., Gay M. E., Matsuoko Y. Nonviral heterogeneous sequences are present at the 5' ends of one species of snowshoe hare bunyavirus S complementary RNA. Nucleic Acids Res. 1983 Sep 24;11(18):6409–6418. doi: 10.1093/nar/11.18.6409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Blanc A., Goyer C., Sonenberg N. The coat protein of the yeast double-stranded RNA virus L-A attaches covalently to the cap structure of eukaryotic mRNA. Mol Cell Biol. 1992 Aug;12(8):3390–3398. doi: 10.1128/mcb.12.8.3390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Blanc A., Ribas J. C., Wickner R. B., Sonenberg N. His-154 is involved in the linkage of the Saccharomyces cerevisiae L-A double-stranded RNA virus Gag protein to the cap structure of mRNAs and is essential for M1 satellite virus expression. Mol Cell Biol. 1994 Apr;14(4):2664–2674. doi: 10.1128/mcb.14.4.2664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Bostian K. A., Sturgeon J. A., Tipper D. J. Encapsidation of yeast killer double-stranded ribonucleic acids: dependence of M on L. J Bacteriol. 1980 Jul;143(1):463–470. doi: 10.1128/jb.143.1.463-470.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Bouloy M., Plotch S. J., Krug R. M. Globin mRNAs are primers for the transcription of influenza viral RNA in vitro. Proc Natl Acad Sci U S A. 1978 Oct;75(10):4886–4890. doi: 10.1073/pnas.75.10.4886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Brierley I., Digard P., Inglis S. C. Characterization of an efficient coronavirus ribosomal frameshifting signal: requirement for an RNA pseudoknot. Cell. 1989 May 19;57(4):537–547. doi: 10.1016/0092-8674(89)90124-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Brierley I., Rolley N. J., Jenner A. J., Inglis S. C. Mutational analysis of the RNA pseudoknot component of a coronavirus ribosomal frameshifting signal. J Mol Biol. 1991 Aug 20;220(4):889–902. doi: 10.1016/0022-2836(91)90361-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Bruenn J. A. A closely related group of RNA-dependent RNA polymerases from double-stranded RNA viruses. Nucleic Acids Res. 1993 Dec 11;21(24):5667–5669. doi: 10.1093/nar/21.24.5667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Bruenn J. A., Brennan V. E. Yeast viral double-stranded RNAs have heterogeneous 3' termini. Cell. 1980 Apr;19(4):923–933. doi: 10.1016/0092-8674(80)90084-7. [DOI] [PubMed] [Google Scholar]
  16. Bussey H., Boone C., Zhu H., Vernet T., Whiteway M., Thomas D. Y. Genetic and molecular approaches to synthesis and action of the yeast killer toxin. Experientia. 1990 Feb 15;46(2):193–200. doi: 10.1007/BF02027313. [DOI] [PubMed] [Google Scholar]
  17. Bussey H. Proteases and the processing of precursors to secreted proteins in yeast. Yeast. 1988 Mar;4(1):17–26. doi: 10.1002/yea.320040103. [DOI] [PubMed] [Google Scholar]
  18. CASPAR D. L., KLUG A. Physical principles in the construction of regular viruses. Cold Spring Harb Symp Quant Biol. 1962;27:1–24. doi: 10.1101/sqb.1962.027.001.005. [DOI] [PubMed] [Google Scholar]
  19. Carroll K., Wickner R. B. Translation and M1 double-stranded RNA propagation: MAK18 = RPL41B and cycloheximide curing. J Bacteriol. 1995 May;177(10):2887–2891. doi: 10.1128/jb.177.10.2887-2891.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Chen D., Zeng C. Q., Wentz M. J., Gorziglia M., Estes M. K., Ramig R. F. Template-dependent, in vitro replication of rotavirus RNA. J Virol. 1994 Nov;68(11):7030–7039. doi: 10.1128/jvi.68.11.7030-7039.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Cheng R. H., Caston J. R., Wang G. J., Gu F., Smith T. J., Baker T. S., Bozarth R. F., Trus B. L., Cheng N., Wickner R. B. Fungal virus capsids, cytoplasmic compartments for the replication of double-stranded RNA, formed as icosahedral shells of asymmetric Gag dimers. J Mol Biol. 1994 Dec 2;244(3):255–258. doi: 10.1006/jmbi.1994.1726. [DOI] [PubMed] [Google Scholar]
  22. Cleveland D. R., Zarbl H., Millward S. Reovirus guanylyltransferase is L2 gene product lambda 2. J Virol. 1986 Oct;60(1):307–311. doi: 10.1128/jvi.60.1.307-311.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Cooper A., Bussey H. Characterization of the yeast KEX1 gene product: a carboxypeptidase involved in processing secreted precursor proteins. Mol Cell Biol. 1989 Jun;9(6):2706–2714. doi: 10.1128/mcb.9.6.2706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Dangel A. W., Shen L., Mendoza A. R., Wu L. C., Yu C. Y. Human helicase gene SKI2W in the HLA class III region exhibits striking structural similarities to the yeast antiviral gene SKI2 and to the human gene KIAA0052: emergence of a new gene family. Nucleic Acids Res. 1995 Jun 25;23(12):2120–2126. doi: 10.1093/nar/23.12.2120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Dihanich M., van Tuinen E., Lambris J. D., Marshallsay B. Accumulation of viruslike particles in a yeast mutant lacking a mitochondrial pore protein. Mol Cell Biol. 1989 Mar;9(3):1100–1108. doi: 10.1128/mcb.9.3.1100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Dinman J. D., Icho T., Wickner R. B. A -1 ribosomal frameshift in a double-stranded RNA virus of yeast forms a gag-pol fusion protein. Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):174–178. doi: 10.1073/pnas.88.1.174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Dinman J. D. Ribosomal frameshifting in yeast viruses. Yeast. 1995 Sep 30;11(12):1115–1127. doi: 10.1002/yea.320111202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Dinman J. D., Wickner R. B. 5 S rRNA is involved in fidelity of translational reading frame. Genetics. 1995 Sep;141(1):95–105. doi: 10.1093/genetics/141.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Dinman J. D., Wickner R. B. Ribosomal frameshifting efficiency and gag/gag-pol ratio are critical for yeast M1 double-stranded RNA virus propagation. J Virol. 1992 Jun;66(6):3669–3676. doi: 10.1128/jvi.66.6.3669-3676.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Dinman J. D., Wickner R. B. Translational maintenance of frame: mutants of Saccharomyces cerevisiae with altered -1 ribosomal frameshifting efficiencies. Genetics. 1994 Jan;136(1):75–86. doi: 10.1093/genetics/136.1.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Dmochowska A., Dignard D., Henning D., Thomas D. Y., Bussey H. Yeast KEX1 gene encodes a putative protease with a carboxypeptidase B-like function involved in killer toxin and alpha-factor precursor processing. Cell. 1987 Aug 14;50(4):573–584. doi: 10.1016/0092-8674(87)90030-4. [DOI] [PubMed] [Google Scholar]
  32. Esteban L. M., Rodriguez-Cousiño N., Esteban R. T double-stranded RNA (dsRNA) sequence reveals that T and W dsRNAs form a new RNA family in Saccharomyces cerevisiae. Identification of 23 S RNA as the single-stranded form of T dsRNA. J Biol Chem. 1992 May 25;267(15):10874–10881. [PubMed] [Google Scholar]
  33. Esteban R., Fujimura T., Wickner R. B. Internal and terminal cis-acting sites are necessary for in vitro replication of the L-A double-stranded RNA virus of yeast. EMBO J. 1989 Mar;8(3):947–954. doi: 10.1002/j.1460-2075.1989.tb03456.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Esteban R., Fujimura T., Wickner R. B. Site-specific binding of viral plus single-stranded RNA to replicase-containing open virus-like particles of yeast. Proc Natl Acad Sci U S A. 1988 Jun;85(12):4411–4415. doi: 10.1073/pnas.85.12.4411. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Esteban R., Wickner R. B. A deletion mutant of L-A double-stranded RNA replicates like M1 double-stranded RNA. J Virol. 1988 Apr;62(4):1278–1285. doi: 10.1128/jvi.62.4.1278-1285.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Esteban R., Wickner R. B. A new non-mendelian genetic element of yeast that increases cytopathology produced by M1 double-stranded RNA in ski strains. Genetics. 1987 Nov;117(3):399–408. doi: 10.1093/genetics/117.3.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Esteban R., Wickner R. B. Three different M1 RNA-containing viruslike particle types in Saccharomyces cerevisiae: in vitro M1 double-stranded RNA synthesis. Mol Cell Biol. 1986 May;6(5):1552–1561. doi: 10.1128/mcb.6.5.1552. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Everett J. G., Gallie D. R. RNA delivery in Saccharomyces cerevisiae using electroporation. Yeast. 1992 Dec;8(12):1007–1014. doi: 10.1002/yea.320081203. [DOI] [PubMed] [Google Scholar]
  39. Farabaugh P. J. Alternative readings of the genetic code. Cell. 1993 Aug 27;74(4):591–596. doi: 10.1016/0092-8674(93)90507-M. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Field L. J., Bobek L. A., Brennan V. E., Reilly J. D., Bruenn J. A. There are at least two yeast viral double-stranded RNAs of the same size: an explanation for viral exclusion. Cell. 1982 Nov;31(1):193–200. doi: 10.1016/0092-8674(82)90419-6. [DOI] [PubMed] [Google Scholar]
  41. Fink G. R., Styles C. A. Curing of a killer factor in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1972 Oct;69(10):2846–2849. doi: 10.1073/pnas.69.10.2846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Fried H. M., Fink G. R. Electron microscopic heteroduplex analysis of "killer" double-stranded RNA species from yeast. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4224–4228. doi: 10.1073/pnas.75.9.4224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Fried H. M., Warner J. R. Molecular cloning and analysis of yeast gene for cycloheximide resistance and ribosomal protein L29. Nucleic Acids Res. 1982 May 25;10(10):3133–3148. doi: 10.1093/nar/10.10.3133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Frilander M., Gottlieb P., Strassman J., Bamford D. H., Mindich L. Dependence of minus-strand synthesis on complete genomic packaging in the double-stranded RNA bacteriophage phi 6. J Virol. 1992 Aug;66(8):5013–5017. doi: 10.1128/jvi.66.8.5013-5017.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Fujimura T., Esteban R., Esteban L. M., Wickner R. B. Portable encapsidation signal of the L-A double-stranded RNA virus of S. cerevisiae. Cell. 1990 Aug 24;62(4):819–828. doi: 10.1016/0092-8674(90)90125-x. [DOI] [PubMed] [Google Scholar]
  46. Fujimura T., Esteban R., Wickner R. B. In vitro L-A double-stranded RNA synthesis in virus-like particles from Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1986 Jun;83(12):4433–4437. doi: 10.1073/pnas.83.12.4433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Fujimura T., Ribas J. C., Makhov A. M., Wickner R. B. Pol of gag-pol fusion protein required for encapsidation of viral RNA of yeast L-A virus. Nature. 1992 Oct 22;359(6397):746–749. doi: 10.1038/359746a0. [DOI] [PubMed] [Google Scholar]
  48. Fujimura T., Wickner R. B. Gene overlap results in a viral protein having an RNA binding domain and a major coat protein domain. Cell. 1988 Nov 18;55(4):663–671. doi: 10.1016/0092-8674(88)90225-5. [DOI] [PubMed] [Google Scholar]
  49. Fujimura T., Wickner R. B. Interaction of two cis sites with the RNA replicase of the yeast L-A virus. J Biol Chem. 1992 Feb 5;267(4):2708–2713. [PubMed] [Google Scholar]
  50. Fujimura T., Wickner R. B. Reconstitution of template-dependent in vitro transcriptase activity of a yeast double-stranded RNA virus. J Biol Chem. 1989 Jun 25;264(18):10872–10877. [PubMed] [Google Scholar]
  51. Fujimura T., Wickner R. B. Replicase of L-A virus-like particles of Saccharomyces cerevisiae. In vitro conversion of exogenous L-A and M1 single-stranded RNAs to double-stranded form. J Biol Chem. 1988 Jan 5;263(1):454–460. [PubMed] [Google Scholar]
  52. Furfine E. S., Wang C. C. Transfection of the Giardia lamblia double-stranded RNA virus into giardia lamblia by electroporation of a single-stranded RNA copy of the viral genome. Mol Cell Biol. 1990 Jul;10(7):3659–3662. doi: 10.1128/mcb.10.7.3659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Furuichi Y., Muthukrishnan S., Tomasz J., Shatkin A. J. Mechanism of formation of reovirus mRNA 5'-terminal blocked and methylated sequence, m7GpppGmpC. J Biol Chem. 1976 Aug 25;251(16):5043–5053. [PubMed] [Google Scholar]
  54. Ghabrial S. A., Havens W. M. The Helminthosporium victoriae 190S mycovirus has two forms distinguishable by capsid protein composition and phosphorylation state. Virology. 1992 Jun;188(2):657–665. doi: 10.1016/0042-6822(92)90520-y. [DOI] [PubMed] [Google Scholar]
  55. Ghabrial S. A. New developments in fungal virology. Adv Virus Res. 1994;43:303–388. doi: 10.1016/S0065-3527(08)60052-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Gottlieb P., Qiao X., Strassman J., Frilander M., Mindich L. Identification of the packaging regions within the genomic RNA segments of bacteriophage phi 6. Virology. 1994 Apr;200(1):42–47. doi: 10.1006/viro.1994.1160. [DOI] [PubMed] [Google Scholar]
  57. HARRIS J. I., HINDLEY J. The protein subunit of turnip yellow mosaic virus. J Mol Biol. 1961 Feb;3:117–120. doi: 10.1016/s0022-2836(61)80014-4. [DOI] [PubMed] [Google Scholar]
  58. Hannig E. M., Leibowitz M. J., Wickner R. B. On the mechanism of exclusion of M2 double-stranded RNA by L-A-E double-stranded RNA in Saccharomyces cerevisiae. Yeast. 1985 Sep;1(1):57–65. doi: 10.1002/yea.320010107. [DOI] [PubMed] [Google Scholar]
  59. Hannig E. M., Thiele D. J., Leibowitz M. J. Saccharomyces cerevisiae killer virus transcripts contain template-coded polyadenylate tracts. Mol Cell Biol. 1984 Jan;4(1):101–109. doi: 10.1128/mcb.4.1.101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Hatfield D. L., Levin J. G., Rein A., Oroszlan S. Translational suppression in retroviral gene expression. Adv Virus Res. 1992;41:193–239. doi: 10.1016/S0065-3527(08)60037-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Hsu C. L., Stevens A. Yeast cells lacking 5'-->3' exoribonuclease 1 contain mRNA species that are poly(A) deficient and partially lack the 5' cap structure. Mol Cell Biol. 1993 Aug;13(8):4826–4835. doi: 10.1128/mcb.13.8.4826. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Hutchins K., Bussey H. Cell wall receptor for yeast killer toxin: involvement of (1 leads to 6)-beta-D-glucan. J Bacteriol. 1983 Apr;154(1):161–169. doi: 10.1128/jb.154.1.161-169.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Icho T., Wickner R. B. The MAK11 protein is essential for cell growth and replication of M double-stranded RNA and is apparently a membrane-associated protein. J Biol Chem. 1988 Jan 25;263(3):1467–1475. [PubMed] [Google Scholar]
  64. Icho T., Wickner R. B. The double-stranded RNA genome of yeast virus L-A encodes its own putative RNA polymerase by fusing two open reading frames. J Biol Chem. 1989 Apr 25;264(12):6716–6723. [PubMed] [Google Scholar]
  65. Iizuka N., Najita L., Franzusoff A., Sarnow P. Cap-dependent and cap-independent translation by internal initiation of mRNAs in cell extracts prepared from Saccharomyces cerevisiae. Mol Cell Biol. 1994 Nov;14(11):7322–7330. doi: 10.1128/mcb.14.11.7322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Isono K., Isono S. Ribosomal protein modification in Escherichia coli. II. Studies of a mutant lacking the N-terminal acetylation of protein S18. Mol Gen Genet. 1980;177(4):645–651. doi: 10.1007/BF00272675. [DOI] [PubMed] [Google Scholar]
  67. Jacks T., Madhani H. D., Masiarz F. R., Varmus H. E. Signals for ribosomal frameshifting in the Rous sarcoma virus gag-pol region. Cell. 1988 Nov 4;55(3):447–458. doi: 10.1016/0092-8674(88)90031-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Jacks T. Translational suppression in gene expression in retroviruses and retrotransposons. Curr Top Microbiol Immunol. 1990;157:93–124. doi: 10.1007/978-3-642-75218-6_4. [DOI] [PubMed] [Google Scholar]
  69. Janda M., Ahlquist P. RNA-dependent replication, transcription, and persistence of brome mosaic virus RNA replicons in S. cerevisiae. Cell. 1993 Mar 26;72(6):961–970. doi: 10.1016/0092-8674(93)90584-d. [DOI] [PubMed] [Google Scholar]
  70. Jang S. K., Kräusslich H. G., Nicklin M. J., Duke G. M., Palmenberg A. C., Wimmer E. A segment of the 5' nontranslated region of encephalomyocarditis virus RNA directs internal entry of ribosomes during in vitro translation. J Virol. 1988 Aug;62(8):2636–2643. doi: 10.1128/jvi.62.8.2636-2643.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Johnson A. W., Kolodner R. D. Synthetic lethality of sep1 (xrn1) ski2 and sep1 (xrn1) ski3 mutants of Saccharomyces cerevisiae is independent of killer virus and suggests a general role for these genes in translation control. Mol Cell Biol. 1995 May;15(5):2719–2727. doi: 10.1128/mcb.15.5.2719. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Julius D., Schekman R., Thorner J. Glycosylation and processing of prepro-alpha-factor through the yeast secretory pathway. Cell. 1984 Feb;36(2):309–318. doi: 10.1016/0092-8674(84)90224-1. [DOI] [PubMed] [Google Scholar]
  73. Kawakami K., Pande S., Faiola B., Moore D. P., Boeke J. D., Farabaugh P. J., Strathern J. N., Nakamura Y., Garfinkel D. J. A rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiae. Genetics. 1993 Oct;135(2):309–320. doi: 10.1093/genetics/135.2.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  74. Kennell J. C., Moran J. V., Perlman P. S., Butow R. A., Lambowitz A. M. Reverse transcriptase activity associated with maturase-encoding group II introns in yeast mitochondria. Cell. 1993 Apr 9;73(1):133–146. doi: 10.1016/0092-8674(93)90166-n. [DOI] [PubMed] [Google Scholar]
  75. Khoshnan A., Alderete J. F. Multiple double-stranded RNA segments are associated with virus particles infecting Trichomonas vaginalis. J Virol. 1993 Dec;67(12):6950–6955. doi: 10.1128/jvi.67.12.6950-6955.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Kim J., Ljungdahl P. O., Fink G. R. kem mutations affect nuclear fusion in Saccharomyces cerevisiae. Genetics. 1990 Dec;126(4):799–812. doi: 10.1093/genetics/126.4.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Kipling D., Tambini C., Kearsey S. E. rar mutations which increase artificial chromosome stability in Saccharomyces cerevisiae identify transcription and recombination proteins. Nucleic Acids Res. 1991 Apr 11;19(7):1385–1391. doi: 10.1093/nar/19.7.1385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  78. Kraal B., De Graaf J. M., Bakker T. A., Van Beynum G. M., Goedhart M., Bosch L. Structural studies on the coat protein of alfalfa-mosaic virus. Eur J Biochem. 1972 Jun 23;28(1):20–29. doi: 10.1111/j.1432-1033.1972.tb01879.x. [DOI] [PubMed] [Google Scholar]
  79. Kulkarni M. S., Sherman F. NAT2, an essential gene encoding methionine N alpha-acetyltransferase in the yeast Saccharomyces cerevisiae. J Biol Chem. 1994 May 6;269(18):13141–13147. [PubMed] [Google Scholar]
  80. Larimer F. W., Hsu C. L., Maupin M. K., Stevens A. Characterization of the XRN1 gene encoding a 5'-->3' exoribonuclease: sequence data and analysis of disparate protein and mRNA levels of gene-disrupted yeast cells. Gene. 1992 Oct 12;120(1):51–57. doi: 10.1016/0378-1119(92)90008-d. [DOI] [PubMed] [Google Scholar]
  81. Lee S. G., Lee I., Park S. H., Kang C., Song K. Identification and characterization of a human cDNA homologous to yeast SKI2. Genomics. 1995 Feb 10;25(3):660–666. doi: 10.1016/0888-7543(95)80008-a. [DOI] [PubMed] [Google Scholar]
  82. Lee S. I., Umen J. G., Varmus H. E. A genetic screen identifies cellular factors involved in retroviral -1 frameshifting. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6587–6591. doi: 10.1073/pnas.92.14.6587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  83. Lee Y. J., Wickner R. B. MAK10, a glucose-repressible gene necessary for replication of a dsRNA virus of Saccharomyces cerevisiae, has T cell receptor alpha-subunit motifs. Genetics. 1992 Sep;132(1):87–96. doi: 10.1093/genetics/132.1.87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  84. Leibowitz M. J., Wickner R. B. A chromosomal gene required for killer plasmid expression, mating, and spore maturation in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1976 Jun;73(6):2061–2065. doi: 10.1073/pnas.73.6.2061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  85. Leibowitz M. J., Wickner R. B. Pet18: a chromosomal gene required for cell growth and for the maintenance of mitochondrial DNA and the killer plasmid of yeast. Mol Gen Genet. 1978 Oct 4;165(2):115–121. doi: 10.1007/BF00269899. [DOI] [PubMed] [Google Scholar]
  86. Liu D. X., Inglis S. C. Internal entry of ribosomes on a tricistronic mRNA encoded by infectious bronchitis virus. J Virol. 1992 Oct;66(10):6143–6154. doi: 10.1128/jvi.66.10.6143-6154.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  87. MacBeth K. J., Patterson J. L. The short transcript of Leishmania RNA virus is generated by RNA cleavage. J Virol. 1995 Jun;69(6):3458–3464. doi: 10.1128/jvi.69.6.3458-3464.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  88. Maga J. A., Widmer G., LeBowitz J. H. Leishmania RNA virus 1-mediated cap-independent translation. Mol Cell Biol. 1995 Sep;15(9):4884–4889. doi: 10.1128/mcb.15.9.4884. [DOI] [PMC free article] [PubMed] [Google Scholar]
  89. Martinac B., Zhu H., Kubalski A., Zhou X. L., Culbertson M., Bussey H., Kung C. Yeast K1 killer toxin forms ion channels in sensitive yeast spheroplasts and in artificial liposomes. Proc Natl Acad Sci U S A. 1990 Aug;87(16):6228–6232. doi: 10.1073/pnas.87.16.6228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  90. Masison D. C., Blanc A., Ribas J. C., Carroll K., Sonenberg N., Wickner R. B. Decoying the cap- mRNA degradation system by a double-stranded RNA virus and poly(A)- mRNA surveillance by a yeast antiviral system. Mol Cell Biol. 1995 May;15(5):2763–2771. doi: 10.1128/mcb.15.5.2763. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. Matsumoto Y., Fishel R., Wickner R. B. Circular single-stranded RNA replicon in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1990 Oct;87(19):7628–7632. doi: 10.1073/pnas.87.19.7628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Miki T., Knight C. A. The protein subunit of potato virus X. Virology. 1968 Oct;36(2):168–173. doi: 10.1016/0042-6822(68)90132-3. [DOI] [PubMed] [Google Scholar]
  93. Mueller M. W., Allmaier M., Eskes R., Schweyen R. J. Transposition of group II intron aI1 in yeast and invasion of mitochondrial genes at new locations. Nature. 1993 Nov 11;366(6451):174–176. doi: 10.1038/366174a0. [DOI] [PubMed] [Google Scholar]
  94. Muhlrad D., Decker C. J., Parker R. Deadenylation of the unstable mRNA encoded by the yeast MFA2 gene leads to decapping followed by 5'-->3' digestion of the transcript. Genes Dev. 1994 Apr 1;8(7):855–866. doi: 10.1101/gad.8.7.855. [DOI] [PubMed] [Google Scholar]
  95. Muhlrad D., Decker C. J., Parker R. Turnover mechanisms of the stable yeast PGK1 mRNA. Mol Cell Biol. 1995 Apr;15(4):2145–2156. doi: 10.1128/mcb.15.4.2145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  96. Munroe D., Jacobson A. Tales of poly(A): a review. Gene. 1990 Jul 16;91(2):151–158. doi: 10.1016/0378-1119(90)90082-3. [DOI] [PubMed] [Google Scholar]
  97. NARITA K. Isolation of acetylpeptide from enzymic digests of TMV-protein. Biochim Biophys Acta. 1958 Apr;28(1):184–191. doi: 10.1016/0006-3002(58)90445-1. [DOI] [PubMed] [Google Scholar]
  98. Newman A. M., Elliott S. G., McLaughlin C. S., Sutherland P. A., Warner R. C. Replication of double-stranded RNA of the virus-like particles in Saccharomyces cerevisiae. J Virol. 1981 Apr;38(1):263–271. doi: 10.1128/jvi.38.1.263-271.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  99. Nomura N., Miyajima N., Sazuka T., Tanaka A., Kawarabayasi Y., Sato S., Nagase T., Seki N., Ishikawa K., Tabata S. Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1. DNA Res. 1994;1(1):27–35. doi: 10.1093/dnares/1.1.27. [DOI] [PubMed] [Google Scholar]
  100. Ohtake Y., Wickner R. B. KRB1, a suppressor of mak7-1 (a mutant RPL4A), is RPL4B, a second ribosomal protein L4 gene, on a fragment of Saccharomyces chromosome XII. Genetics. 1995 May;140(1):129–137. doi: 10.1093/genetics/140.1.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  101. Ohtake Y., Wickner R. B. Yeast virus propagation depends critically on free 60S ribosomal subunit concentration. Mol Cell Biol. 1995 May;15(5):2772–2781. doi: 10.1128/mcb.15.5.2772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  102. Palmiter R. D., Gagnon J., Vogt V. M., Ripley S., Eisenman R. N. The NH2-terminal sequence of the avian oncovirus gag precursor polyprotein (Pr76gag). Virology. 1978 Dec;91(2):423–433. doi: 10.1016/0042-6822(78)90388-4. [DOI] [PubMed] [Google Scholar]
  103. Patterson J. L., Holloway B., Kolakofsky D. La Crosse virions contain a primer-stimulated RNA polymerase and a methylated cap-dependent endonuclease. J Virol. 1984 Oct;52(1):215–222. doi: 10.1128/jvi.52.1.215-222.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  104. Pelletier J., Sonenberg N. Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA. Nature. 1988 Jul 28;334(6180):320–325. doi: 10.1038/334320a0. [DOI] [PubMed] [Google Scholar]
  105. Plotch S. J., Bouloy M., Ulmanen I., Krug R. M. A unique cap(m7GpppXm)-dependent influenza virion endonuclease cleaves capped RNAs to generate the primers that initiate viral RNA transcription. Cell. 1981 Mar;23(3):847–858. doi: 10.1016/0092-8674(81)90449-9. [DOI] [PubMed] [Google Scholar]
  106. Quadt R., Ishikawa M., Janda M., Ahlquist P. Formation of brome mosaic virus RNA-dependent RNA polymerase in yeast requires coexpression of viral proteins and viral RNA. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4892–4896. doi: 10.1073/pnas.92.11.4892. [DOI] [PMC free article] [PubMed] [Google Scholar]
  107. Rhee S. K., Icho T., Wickner R. B. Structure and nuclear localization signal of the SKI3 antiviral protein of Saccharomyces cerevisiae. Yeast. 1989 May-Jun;5(3):149–158. doi: 10.1002/yea.320050304. [DOI] [PubMed] [Google Scholar]
  108. Ribas J. C., Fujimura T., Wickner R. B. A cryptic RNA-binding domain in the Pol region of the L-A double-stranded RNA virus Gag-Pol fusion protein. J Virol. 1994 Sep;68(9):6014–6020. doi: 10.1128/jvi.68.9.6014-6020.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  109. Ribas J. C., Fujimura T., Wickner R. B. Essential RNA binding and packaging domains of the Gag-Pol fusion protein of the L-A double-stranded RNA virus of Saccharomyces cerevisiae. J Biol Chem. 1994 Nov 11;269(45):28420–28428. [PubMed] [Google Scholar]
  110. Ribas J. C., Wickner R. B. RNA-dependent RNA polymerase consensus sequence of the L-A double-stranded RNA virus: definition of essential domains. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2185–2189. doi: 10.1073/pnas.89.6.2185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  111. Ribas J. C., Wickner R. B. Saccharomyces cerevisiae L-BC double-stranded RNA virus replicase recognizes the L-A positive-strand RNA 3' end. J Virol. 1996 Jan;70(1):292–297. doi: 10.1128/jvi.70.1.292-297.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  112. Ridley S. P., Sommer S. S., Wickner R. B. Superkiller mutations in Saccharomyces cerevisiae suppress exclusion of M2 double-stranded RNA by L-A-HN and confer cold sensitivity in the presence of M and L-A-HN. Mol Cell Biol. 1984 Apr;4(4):761–770. doi: 10.1128/mcb.4.4.761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  113. Russell P. J., Hambidge S. J., Kirkegaard K. Direct introduction and transient expression of capped and non-capped RNA in Saccharomyces cerevisiae. Nucleic Acids Res. 1991 Sep 25;19(18):4949–4953. doi: 10.1093/nar/19.18.4949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  114. Sandmeyer S. B. Yeast retrotransposons. Curr Opin Genet Dev. 1992 Oct;2(5):705–711. doi: 10.1016/s0959-437x(05)80130-3. [DOI] [PubMed] [Google Scholar]
  115. Scheidel L. M., Durbin R. K., Stollar V. SVLM21, a Sindbis virus mutant resistant to methionine deprivation, encodes an altered methyltransferase. Virology. 1989 Dec;173(2):408–414. doi: 10.1016/0042-6822(89)90553-9. [DOI] [PubMed] [Google Scholar]
  116. Schmitt M. J., Tipper D. J. Genetic analysis of maintenance and expression of L and M double-stranded RNAs from yeast killer virus K28. Yeast. 1992 May;8(5):373–384. doi: 10.1002/yea.320080505. [DOI] [PubMed] [Google Scholar]
  117. Schmitt M., Radler F. Mannoprotein of the yeast cell wall as primary receptor for the killer toxin of Saccharomyces cerevisiae strain 28. J Gen Microbiol. 1987 Dec;133(12):3347–3354. doi: 10.1099/00221287-133-12-3347. [DOI] [PubMed] [Google Scholar]
  118. Sclafani R. A., Fangman W. L. Conservative replication of double-stranded RNA in Saccharomyces cerevisiae by displacement of progeny single strands. Mol Cell Biol. 1984 Aug;4(8):1618–1626. doi: 10.1128/mcb.4.8.1618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  119. Sepp T., Entzeroth R., Mertsching J., Hofschneider P. H., Kandolf R. Novel ribonucleic acid species in Eimeria nieschulzi are associated with RNA-dependent RNA polymerase activity. Parasitol Res. 1991;77(7):581–584. doi: 10.1007/BF00931017. [DOI] [PubMed] [Google Scholar]
  120. Shen Y., Bruenn J. A. RNA structural requirements for RNA binding, replication, and packaging in the yeast double-stranded RNA virus. Virology. 1993 Aug;195(2):481–491. doi: 10.1006/viro.1993.1399. [DOI] [PubMed] [Google Scholar]
  121. Sommer S. S., Wickner R. B. Yeast L dsRNA consists of at least three distinct RNAs; evidence that the non-Mendelian genes [HOK], [NEX] and [EXL] are on one of these dsRNAs. Cell. 1982 Dec;31(2 Pt 1):429–441. doi: 10.1016/0092-8674(82)90136-2. [DOI] [PubMed] [Google Scholar]
  122. Somogyi P., Jenner A. J., Brierley I., Inglis S. C. Ribosomal pausing during translation of an RNA pseudoknot. Mol Cell Biol. 1993 Nov;13(11):6931–6940. doi: 10.1128/mcb.13.11.6931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  123. Steiner D. F., Smeekens S. P., Ohagi S., Chan S. J. The new enzymology of precursor processing endoproteases. J Biol Chem. 1992 Nov 25;267(33):23435–23438. [PubMed] [Google Scholar]
  124. Stevens A., Maupin M. K. A 5'----3' exoribonuclease of Saccharomyces cerevisiae: size and novel substrate specificity. Arch Biochem Biophys. 1987 Feb 1;252(2):339–347. doi: 10.1016/0003-9861(87)90040-3. [DOI] [PubMed] [Google Scholar]
  125. Stevens A. Purification and characterization of a Saccharomyces cerevisiae exoribonuclease which yields 5'-mononucleotides by a 5' leads to 3' mode of hydrolysis. J Biol Chem. 1980 Apr 10;255(7):3080–3085. [PubMed] [Google Scholar]
  126. Stucka R., Schwarzlose C., Lochmüller H., Häcker U., Feldmann H. Molecular analysis of the yeast Ty4 element: homology with Ty1, copia, and plant retrotransposons. Gene. 1992 Dec 1;122(1):119–128. doi: 10.1016/0378-1119(92)90039-r. [DOI] [PubMed] [Google Scholar]
  127. Tarr P. I., Aline R. F., Jr, Smiley B. L., Scholler J., Keithly J., Stuart K. LR1: a candidate RNA virus of Leishmania. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9572–9575. doi: 10.1073/pnas.85.24.9572. [DOI] [PMC free article] [PubMed] [Google Scholar]
  128. Tercero J. C., Dinman J. D., Wickner R. B. Yeast MAK3 N-acetyltransferase recognizes the N-terminal four amino acids of the major coat protein (gag) of the L-A double-stranded RNA virus. J Bacteriol. 1993 May;175(10):3192–3194. doi: 10.1128/jb.175.10.3192-3194.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  129. Tercero J. C., Riles L. E., Wickner R. B. Localized mutagenesis and evidence for post-transcriptional regulation of MAK3. A putative N-acetyltransferase required for double-stranded RNA virus propagation in Saccharomyces cerevisiae. J Biol Chem. 1992 Oct 5;267(28):20270–20276. [PubMed] [Google Scholar]
  130. Tercero J. C., Wickner R. B. MAK3 encodes an N-acetyltransferase whose modification of the L-A gag NH2 terminus is necessary for virus particle assembly. J Biol Chem. 1992 Oct 5;267(28):20277–20281. [PubMed] [Google Scholar]
  131. Thrash C., Voelkel K., DiNardo S., Sternglanz R. Identification of Saccharomyces cerevisiae mutants deficient in DNA topoisomerase I activity. J Biol Chem. 1984 Feb 10;259(3):1375–1377. [PubMed] [Google Scholar]
  132. Tipper D. J., Schmitt M. J. Yeast dsRNA viruses: replication and killer phenotypes. Mol Microbiol. 1991 Oct;5(10):2331–2338. doi: 10.1111/j.1365-2958.1991.tb02078.x. [DOI] [PubMed] [Google Scholar]
  133. Tishkoff D. X., Johnson A. W., Kolodner R. D. Molecular and genetic analysis of the gene encoding the Saccharomyces cerevisiae strand exchange protein Sep1. Mol Cell Biol. 1991 May;11(5):2593–2608. doi: 10.1128/mcb.11.5.2593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  134. Toh-E A., Guerry P., Wickner R. B. Chromosomal superkiller mutants of Saccharomyces cerevisiae. J Bacteriol. 1978 Dec;136(3):1002–1007. doi: 10.1128/jb.136.3.1002-1007.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  135. Toh-E A., Wickner R. B. "Superkiller" mutations suppress chromosomal mutations affecting double-stranded RNA killer plasmid replication in saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1980 Jan;77(1):527–530. doi: 10.1073/pnas.77.1.527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  136. Toh-e A., Sahashi Y. The PET18 locus of Saccharomyces cerevisiae: a complex locus containing multiple genes. Yeast. 1985 Dec;1(2):159–171. doi: 10.1002/yea.320010204. [DOI] [PubMed] [Google Scholar]
  137. Tu C., Tzeng T. H., Bruenn J. A. Ribosomal movement impeded at a pseudoknot required for frameshifting. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8636–8640. doi: 10.1073/pnas.89.18.8636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  138. Van Ryk D. I., Lee Y., Nazar R. N. Efficient expression and utilization of mutant 5 S rRNA in Saccharomyces cerevisiae. J Biol Chem. 1990 May 25;265(15):8377–8381. [PubMed] [Google Scholar]
  139. Voytas D. F., Boeke J. D. Yeast retrotransposon revealed. Nature. 1992 Aug 27;358(6389):717–717. doi: 10.1038/358717a0. [DOI] [PubMed] [Google Scholar]
  140. Wagner J. C., Wolf D. H. Hormone (pheromone) processing enzymes in yeast. The carboxy-terminal processing enzyme of the mating pheromone alpha-factor, carboxypeptidase ysc alpha, is absent in alpha-factor maturation-defective kex1 mutant cells. FEBS Lett. 1987 Sep 14;221(2):423–426. doi: 10.1016/0014-5793(87)80967-5. [DOI] [PubMed] [Google Scholar]
  141. Wang A. L., Yang H. M., Shen K. A., Wang C. C. Giardiavirus double-stranded RNA genome encodes a capsid polypeptide and a gag-pol-like fusion protein by a translation frameshift. Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8595–8599. doi: 10.1073/pnas.90.18.8595. [DOI] [PMC free article] [PubMed] [Google Scholar]
  142. Wang A., Wang C. C., Alderete J. F. Trichomonas vaginalis phenotypic variation occurs only among trichomonads infected with the double-stranded RNA virus. J Exp Med. 1987 Jul 1;166(1):142–150. doi: 10.1084/jem.166.1.142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  143. Wesolowski M., Wickner R. B. Two new double-stranded RNA molecules showing non-mendelian inheritance and heat inducibility in Saccharomyces cerevisiae. Mol Cell Biol. 1984 Jan;4(1):181–187. doi: 10.1128/mcb.4.1.181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  144. Wickner R. B., Boutelet F., Hilger F. Evidence for a new chromosome in Saccharomyces cerevisiae. Mol Cell Biol. 1983 Mar;3(3):415–420. doi: 10.1128/mcb.3.3.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  145. Wickner R. B. Chromosomal and nonchromosomal mutations affecting the "killer character" of Saccharomyces cerevisiae. Genetics. 1974 Mar;76(3):423–432. doi: 10.1093/genetics/76.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  146. Wickner R. B. Double-stranded and single-stranded RNA viruses of Saccharomyces cerevisiae. Annu Rev Microbiol. 1992;46:347–375. doi: 10.1146/annurev.mi.46.100192.002023. [DOI] [PubMed] [Google Scholar]
  147. Wickner R. B. Host function of MAK16: G1 arrest by a mak16 mutant of Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1988 Aug;85(16):6007–6011. doi: 10.1073/pnas.85.16.6007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  148. Wickner R. B., Icho T., Fujimura T., Widner W. R. Expression of yeast L-A double-stranded RNA virus proteins produces derepressed replication: a ski- phenocopy. J Virol. 1991 Jan;65(1):155–161. doi: 10.1128/jvi.65.1.155-161.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  149. Wickner R. B. Killer systems in Saccharomyces cerevisiae: three distinct modes of exclusion of M2 double-stranded RNA by three species of double-stranded RNA, M1, L-A-E, and L-A-HN. Mol Cell Biol. 1983 Apr;3(4):654–661. doi: 10.1128/mcb.3.4.654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  150. Wickner R. B., Leibowitz M. J. Chromosomal genes essential for replication of a double-stranded RNA plasmid of Saccharomyces cerevisiae: the killer character of yeast. J Mol Biol. 1976 Aug 15;105(3):427–443. doi: 10.1016/0022-2836(76)90102-9. [DOI] [PubMed] [Google Scholar]
  151. Wickner R. B. MKT1, a nonessential Saccharomyces cerevisiae gene with a temperature-dependent effect on replication of M2 double-stranded RNA. J Bacteriol. 1987 Nov;169(11):4941–4945. doi: 10.1128/jb.169.11.4941-4945.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  152. Wickner R. B. Mapping chromosomal genes of Saccharomyces cerevisiae using an improved genetic mapping method. Genetics. 1979 Jul;92(3):803–821. doi: 10.1093/genetics/92.3.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  153. Wickner R. B. Plasmids controlled exclusion of the K2 killer double-stranded RNA plasmid of yeast. Cell. 1980 Aug;21(1):217–226. doi: 10.1016/0092-8674(80)90129-4. [DOI] [PubMed] [Google Scholar]
  154. Wickner R. B., Ridley S. P., Fried H. M., Ball S. G. Ribosomal protein L3 is involved in replication or maintenance of the killer double-stranded RNA genome of Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4706–4708. doi: 10.1073/pnas.79.15.4706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  155. Wickner R. B., Toh-e A. [HOK], a new yeast non-Mendelian trait, enables a replication-defective killer plasmid to be maintained. Genetics. 1982 Feb;100(2):159–174. doi: 10.1093/genetics/100.2.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  156. Wickner R. B. Twenty-six chromosomal genes needed to maintain the killer double-stranded RNA plasmid of Saccharomyces cerevisiae. Genetics. 1978 Mar;88(3):419–425. doi: 10.1093/genetics/88.3.419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  157. Wickner R. B. [URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae. Science. 1994 Apr 22;264(5158):566–569. doi: 10.1126/science.7909170. [DOI] [PubMed] [Google Scholar]
  158. Widner W. R., Wickner R. B. Evidence that the SKI antiviral system of Saccharomyces cerevisiae acts by blocking expression of viral mRNA. Mol Cell Biol. 1993 Jul;13(7):4331–4341. doi: 10.1128/mcb.13.7.4331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  159. Xu H., Boeke J. D. Host genes that influence transposition in yeast: the abundance of a rare tRNA regulates Ty1 transposition frequency. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8360–8364. doi: 10.1073/pnas.87.21.8360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  160. Yoshikawa A., Isono S., Sheback A., Isono K. Cloning and nucleotide sequencing of the genes rimI and rimJ which encode enzymes acetylating ribosomal proteins S18 and S5 of Escherichia coli K12. Mol Gen Genet. 1987 Oct;209(3):481–488. doi: 10.1007/BF00331153. [DOI] [PubMed] [Google Scholar]

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