Tie-Break: Host and Retrotransposons Play tRNA

Trends Cell Biol. 2018 Oct;28(10):793-806. doi: 10.1016/j.tcb.2018.05.006. Epub 2018 Jun 19.

Abstract

tRNA fragments (tRFs) are a class of small, regulatory RNAs with diverse functions. 3'-Derived tRFs perfectly match long terminal repeat (LTR)-retroelements which use the 3'-end of tRNAs to prime reverse transcription. Recent work has shown that tRFs target LTR-retroviruses and -transposons for the RNA interference (RNAi) pathway and also inhibit mobility by blocking reverse transcription. The highly conserved tRNA primer binding site (PBS) in LTR-retroelements is a unique target for 3'-tRFs to recognize and block abundant but diverse LTR-retrotransposons that become transcriptionally active during epigenetic reprogramming in development and disease. 3'-tRFs are processed from full-length tRNAs under so far unknown conditions and potentially protect many cell types. tRFs appear to be an ancient link between RNAi, transposons, and genome stability.

Keywords: LTR-retrotransposon; primer binding site; retrovirus; small RNA; tRF; tRNA.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Binding Sites
  • Humans
  • RNA, Transfer* / genetics
  • RNA, Transfer* / metabolism
  • Retroelements / genetics*

Substances

  • Retroelements
  • RNA, Transfer