A novel narnavirus is widespread in Saccharomyces cerevisiae and impacts multiple host phenotypes

被引:3
|
作者
Vijayraghavan, Sriram [1 ,2 ]
Kozmin, Stanislav G. [1 ]
Xi, Wen [1 ]
McCusker, John H. [1 ,3 ]
机构
[1] Duke Univ Med Ctr, Dept Mol Genet & Microbiol, Jones Bldg Room 239,561 Res Dr 3020,Jones Bldg Roo, Durham, NC 27710 USA
[2] Med Univ South Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[3] Duke Univ Med Ctr, Dept Mol Genet & Microbiol, Jones Bldg Room 239,561 Res Dr 3020, Durham, NC 27710 USA
来源
G3-GENES GENOMES GENETICS | 2023年 / 13卷 / 02期
关键词
RNA viruses; narnavirus; autophagy; Ras; PKA; 100-genomes strains; Saccharomyces cerevisiae; DOUBLE-STRANDED-RNA; YEAST; VIRUSES; PROTEIN; AUTOPHAGY; PRIONS; KINASE; DNA; PHOSPHODIESTERASE; ACCURATE;
D O I
10.1093/g3journal/jkac337
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
RNA viruses are a widespread, biologically diverse group that includes the narnaviridiae, a family of unencapsidated RNA viruses containing a single ORF that encodes an RNA-dependent RNA polymerase. In the yeast Saccharomyces cerevisiae, the 20S and 23S RNA viruses are well-studied members of the narnaviridiae, which are present at low intracellular copy numbers, unless induced by stress or unfavorable growth conditions, and are not known to affect host fitness. In this study, we describe a new S. cerevisiae narnavirus that we designate as N1199. We show that N1199 is uniquely present as a double-stranded RNA at a high level relative to other known members of this family in 1 strain background, YJM1199, and is present as a single-stranded RNA at lower levels in 98 of the remaining 100-genomes strains. Furthermore, we see a strong association between the presence of high level N1199 and host phenotype defects, including greatly reduced sporulation efficiency and growth on multiple carbon sources. Finally, we describe associations between N1199 abundance and host phenotype defects, including autophagy.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
    Kawashima, Tadashi
    Douglass, Stephen
    Gabunilas, Jason
    Pellegrini, Matteo
    Chanfreau, Guillaume F.
    PLOS GENETICS, 2014, 10 (04):
  • [32] Saccharomyces cerevisiae- Insects Association: Impacts, Biogeography, and Extent
    Meriggi, Niccolo'
    Di Paola, Monica
    Cavalieri, Duccio
    Stefanini, Irene
    FRONTIERS IN MICROBIOLOGY, 2020, 11
  • [33] Identification of a novel lysophospholipid acyltransferase in Saccharomyces cerevisiae
    Jain, Shilpa
    Stanford, NaTaza
    Bhagwat, Neha
    Seiler, Brian
    Costanzo, Michael
    Boone, Charles
    Oelkers, Peter
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (42) : 30562 - 30569
  • [34] A novel pathway of ceramide metabolism in Saccharomyces cerevisiae
    Voynova, Natalia S.
    Vionnet, Christine
    Ejsing, Christer S.
    Conzelmann, Andreas
    BIOCHEMICAL JOURNAL, 2012, 447 : 103 - 114
  • [35] A novel method for subcellular fractionation of Saccharomyces cerevisiae
    Blackwell, KJ
    White, JS
    Tobin, JM
    BIOTECHNOLOGY TECHNIQUES, 1999, 13 (09) : 583 - 587
  • [36] A novel assay for replicative lifespan in Saccharomyces cerevisiae
    Jarolim, S
    Millen, J
    Heeren, G
    Laun, P
    Goldfarb, DS
    Breitenbach, M
    FEMS YEAST RESEARCH, 2004, 5 (02) : 169 - 177
  • [37] Novel methods of genome shuffling in Saccharomyces cerevisiae
    Lihua Hou
    Biotechnology Letters, 2009, 31 : 671 - 677
  • [38] Novel methods of genome shuffling in Saccharomyces cerevisiae
    Hou, Lihua
    BIOTECHNOLOGY LETTERS, 2009, 31 (05) : 671 - 677
  • [40] Saccharomyces cerevisiae as host for the recombinant production of polyketides and nonribosomal peptides
    Tippelt, Anna
    Nett, Markus
    MICROBIAL CELL FACTORIES, 2021, 20 (01)