PPR-SMR protein SOT1 has RNA endonuclease activity

Proc Natl Acad Sci U S A. 2017 Feb 21;114(8):E1554-E1563. doi: 10.1073/pnas.1612460114. Epub 2017 Feb 6.

Abstract

Numerous attempts have been made to identify and engineer sequence-specific RNA endonucleases, as these would allow for efficient RNA manipulation. However, no natural RNA endonuclease that recognizes RNA in a sequence-specific manner has been described to date. Here, we report that SUPPRESSOR OF THYLAKOID FORMATION 1 (SOT1), an Arabidopsis pentatricopeptide repeat (PPR) protein with a small MutS-related (SMR) domain, has RNA endonuclease activity. We show that the SMR moiety of SOT1 performs the endonucleolytic maturation of 23S and 4.5S rRNA through the PPR domain, specifically recognizing a 13-nucleotide RNA sequence in the 5' end of the chloroplast 23S-4.5S rRNA precursor. In addition, we successfully engineered the SOT1 protein with altered PPR motifs to recognize and cleave a predicted RNA substrate. Our findings point to SOT1 as an exciting tool for RNA manipulation.

Keywords: PPR-SMR protein; RNA endonuclease; photosynthesis; rRNA biogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / enzymology*
  • Arabidopsis / genetics
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Chloroplasts / genetics
  • Chloroplasts / metabolism
  • Electrophoretic Mobility Shift Assay
  • Endoribonucleases / genetics
  • Endoribonucleases / metabolism*
  • Genetic Engineering
  • Membrane Proteins / metabolism
  • Protein Biosynthesis
  • RNA, Chloroplast / metabolism*
  • RNA, Ribosomal, 23S / metabolism
  • Recombinant Proteins / metabolism
  • Thylakoids / metabolism*

Substances

  • Arabidopsis Proteins
  • Membrane Proteins
  • RNA, Chloroplast
  • RNA, Ribosomal, 23S
  • Recombinant Proteins
  • THF1 protein, Arabidopsis
  • pentatricopeptide repeat protein, Arabidopsis
  • Endoribonucleases