A noncoding RNA produced by arthropod-borne flaviviruses inhibits the cellular exoribonuclease XRN1 and alters host mRNA stability

• Published in: RNA (Cambridge) Vol. 18; no. 11; pp. 2029 - 2040
• Main Authors: Moon, Stephanie L, Anderson, John R, Kumagai, Yutaro, Wilusz, Carol J, Akira, Shizuo, Khromykh, Alexander A, Wilusz, Jeffrey
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 01.11.2012
• Subjects: 3' Untranslated Regions; Aedes - cytology; Aedes - virology; Animals; Cell Line; Cricetinae; Dengue Virus - genetics; Dengue Virus - physiology; Exoribonucleases - antagonists & inhibitors; Exoribonucleases - chemistry; Exoribonucleases - metabolism; Gene Expression Regulation; Half-Life; Host-Pathogen Interactions; Humans; Insect Proteins - antagonists & inhibitors; Insect Proteins - chemistry; Insect Proteins - metabolism; Microtubule-Associated Proteins - antagonists & inhibitors; Microtubule-Associated Proteins - chemistry; Microtubule-Associated Proteins - metabolism; Oligonucleotide Array Sequence Analysis; RNA Stability; RNA, Messenger - chemistry; RNA, Messenger - metabolism; RNA, Untranslated - chemistry; RNA, Untranslated - metabolism; RNA, Untranslated - physiology; RNA, Viral - chemistry; RNA, Viral - metabolism; RNA, Viral - physiology; Saccharomyces cerevisiae Proteins - antagonists & inhibitors; Saccharomyces cerevisiae Proteins - chemistry; Transcriptome; West Nile virus - genetics; West Nile virus - physiology
• ISSN: 1355-8382; 1469-9001
• DOI: 10.1261/rna.034330.112

All arthropod-borne flaviviruses generate a short noncoding RNA (sfRNA) from the viral 3' untranslated region during infection due to stalling of the cellular 5'-to-3' exonuclease XRN1. We show here that formation of sfRNA also inhibits XRN1 activity. Cells infected with Dengue or Kunjin viruses accumulate uncapped mRNAs, decay intermediates normally targeted by XRN1. XRN1 repression also resulted in the increased overall stability of cellular mRNAs in flavivirus-infected cells. Importantly, a mutant Kunjin virus that cannot form sfRNA but replicates to normal levels failed to affect host mRNA stability or XRN1 activity. Expression of sfRNA in the absence of viral infection demonstrated that sfRNA formation was directly responsible for the stabilization of cellular mRNAs. Finally, numerous cellular mRNAs were differentially expressed in an sfRNA-dependent fashion in a Kunjin virus infection. We conclude that flaviviruses incapacitate XRN1 during infection and dysregulate host mRNA stability as a result of sfRNA formation.