Biogenesis of RNase P RNA from an intron requires co-assembly with cognate protein subunits

Nucleic Acids Res. 2019 Sep 19;47(16):8746-8754. doi: 10.1093/nar/gkz572.

Abstract

RNase P RNA (RPR), the catalytic subunit of the essential RNase P ribonucleoprotein, removes the 5' leader from precursor tRNAs. The ancestral eukaryotic RPR is a Pol III transcript generated with mature termini. In the branch of the arthropod lineage that led to the insects and crustaceans, however, a new allele arose in which RPR is embedded in an intron of a Pol II transcript and requires processing from intron sequences for maturation. We demonstrate here that the Drosophila intronic-RPR precursor is trimmed to the mature form by the ubiquitous nuclease Rat1/Xrn2 (5') and the RNA exosome (3'). Processing is regulated by a subset of RNase P proteins (Rpps) that protects the nascent RPR from degradation, the typical fate of excised introns. Our results indicate that the biogenesis of RPR in vivo entails interaction of Rpps with the nascent RNA to form the RNase P holoenzyme and suggests that a new pathway arose in arthropods by coopting ancient mechanisms common to processing of other noncoding RNAs.

Publication types

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

MeSH terms

  • Alternative Splicing*
  • Animals
  • Biological Evolution
  • Cell Line
  • Computational Biology / methods
  • DNA-Directed RNA Polymerases / genetics
  • DNA-Directed RNA Polymerases / metabolism
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / enzymology
  • Drosophila melanogaster / genetics
  • Embryo, Nonmammalian
  • Exons
  • Exoribonucleases / genetics
  • Exoribonucleases / metabolism
  • Introns
  • Macrophages / cytology
  • Macrophages / enzymology
  • Male
  • Nucleic Acid Conformation
  • Protein Subunits / genetics*
  • Protein Subunits / metabolism
  • Proteolysis
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • RNA, Transfer / genetics*
  • RNA, Transfer / metabolism
  • Ribonuclease P / genetics*
  • Ribonuclease P / metabolism

Substances

  • Drosophila Proteins
  • Protein Subunits
  • RNA, Messenger
  • RNA, Transfer
  • DNA-Directed RNA Polymerases
  • Exoribonucleases
  • Ribonuclease P