Abstract
The processing of precursor tRNAs at their 5′ and 3′ termini is a fundamental event in the biosynthesis of tRNA. RNase P is generally responsible for endonucleolytic removal of a leader sequence of precursor tRNA to generate the mature 5′ terminus. However, much less is known about the RNase P counterparts or other proteins that are active at the tRNA 3′ terminus. Here we show that one of the human RNase P subunits, Rpp14, together with one of its interacting protein partners, OIP2, is a 3′→5′ exoribonuclease with a phosphorolytic activity that processes the 3′ terminus of precursor tRNA. Immunoprecipitates of a crude human RNase P complex can process both ends of precursor tRNA by hydrolysis, but purified RNase P has no exonuclease activity. Rpp14 and OIP2 may be part of an exosome activity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 5295-5300 |
| Number of pages | 6 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 99 |
| Issue number | 8 |
| DOIs | |
| State | Published - Apr 16 2002 |
| Externally published | Yes |
Keywords
- Exosome
- Phosphorolytic enzymes
- tRNA processing
ASJC Scopus subject areas
- General
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