1. Genome-wide mapping of infection-induced SINE RNAs reveals a role in selective mRNA export.
- Author
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Karijolich J, Zhao Y, Alla R, and Glaunsinger B
- Subjects
- Animals, Biological Transport genetics, Cell Cycle Proteins genetics, Gene Knockdown Techniques, Herpesviridae Infections genetics, Mice, NIH 3T3 Cells, Nuclear Matrix-Associated Proteins metabolism, RNA Interference, RNA Polymerase III genetics, RNA, Messenger metabolism, RNA-Binding Proteins metabolism, Retroelements physiology, Rhadinovirus, Sequence Analysis, DNA, Stress, Physiological genetics, Subcellular Fractions metabolism, Transcription, Genetic, Tumor Virus Infections genetics, Gene Expression Regulation genetics, RNA, Messenger genetics, Short Interspersed Nucleotide Elements genetics
- Abstract
Short interspersed nuclear elements (SINEs) are retrotransposons evolutionarily derived from endogenous RNA Polymerase III RNAs. Though SINE elements have undergone exaptation into gene regulatory elements, how transcribed SINE RNA impacts transcriptional and post-transcriptional regulation is largely unknown. This is partly due to a lack of information regarding which of the loci have transcriptional potential. Here, we present an approach (short interspersed nuclear element sequencing, SINE-seq), which selectively profiles RNA Polymerase III-derived SINE RNA, thereby identifying transcriptionally active SINE loci. Applying SINE-seq to monitor murine B2 SINE expression during a gammaherpesvirus infection revealed transcription from 28 270 SINE loci, with ∼50% of active SINE elements residing within annotated RNA Polymerase II loci. Furthermore, B2 RNA can form intermolecular RNA-RNA interactions with complementary mRNAs, leading to nuclear retention of the targeted mRNA via a mechanism involving p54nrb. These findings illuminate a pathway for the selective regulation of mRNA export during stress via retrotransposon activation., (© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.)
- Published
- 2017
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