Mapping the Small RNA Content of Simian Immunodeficiency Virions (SIV)

Recent evidence indicates that regulatory small non-coding RNAs are not only components of eukaryotic cells and vesicles, but also reside within a number of different viruses including retroviral particles. Using ultra-deep sequencing we have comprehensively analyzed the content of simian immunodefi...

Full description

Saved in:
Bibliographic Details
Published inPloS one Vol. 8; no. 9; p. e75063
Main Authors Brameier, Markus, Ibing, Wiebke, Höfer, Katharina, Montag, Judith, Stahl-Hennig, Christiane, Motzkus, Dirk
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 23.09.2013
Public Library of Science (PLoS)
Subjects
Online AccessGet full text
ISSN1932-6203
1932-6203
DOI10.1371/journal.pone.0075063

Cover

More Information
Summary:Recent evidence indicates that regulatory small non-coding RNAs are not only components of eukaryotic cells and vesicles, but also reside within a number of different viruses including retroviral particles. Using ultra-deep sequencing we have comprehensively analyzed the content of simian immunodeficiency virions (SIV), which were compared to mock-control preparations. Our analysis revealed that more than 428,000 sequence reads matched the SIV mac239 genome sequence. Among these we could identify 12 virus-derived small RNAs (vsRNAs) that were highly abundant. Beside known retrovirus-enriched small RNAs, like 7SL-RNA, tRNA(Lys3) and tRNA(Lys) isoacceptors, we also identified defined fragments derived from small ILF3/NF90-associated RNA snaR-A14, that were enriched more than 50 fold in SIV. We also found evidence that small nucleolar RNAs U2 and U12 were underrepresented in the SIV preparation, indicating that the relative number or the content of co-isolated exosomes was changed upon infection. Our comprehensive atlas of SIV-incorporated small RNAs provides a refined picture of the composition of retrovirions, which gives novel insights into viral packaging.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
Competing Interests: The authors have declared that no competing interests exist.
Current address: Molecular and Cellular Physiology, Hannover Medical School, Hannover, Germany
Conceived and designed the experiments: DM. Performed the experiments: WI KH. Analyzed the data: DM MB JM. Contributed reagents/materials/analysis tools: CSH. Wrote the manuscript: MB KH JM CSH DM.
Current address: Department of Vascular and Endovascular Surgery, Düsseldorf University Hospital, Düsseldorf, Germany
Current address: Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Heidelberg, Germany
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0075063