Structural Organization of S516 Group I Introns in Myxomycetes

Genes (Basel). 2022 May 25;13(6):944. doi: 10.3390/genes13060944.

Abstract

Group I introns are mobile genetic elements encoding self-splicing ribozymes. Group I introns in nuclear genes are restricted to ribosomal DNA of eukaryotic microorganisms. For example, the myxomycetes, which represent a distinct protist phylum with a unique life strategy, are rich in nucleolar group I introns. We analyzed and compared 75 group I introns at position 516 in the small subunit ribosomal DNA from diverse and distantly related myxomycete taxa. A consensus secondary structure revealed a conserved group IC1 ribozyme core, but with a surprising RNA sequence complexity in the peripheral regions. Five S516 group I introns possess a twintron organization, where a His-Cys homing endonuclease gene insertion was interrupted by a small spliceosomal intron. Eleven S516 introns contained direct repeat arrays with varying lengths of the repeated motif, a varying copy number, and different structural organizations. Phylogenetic analyses of S516 introns and the corresponding host genes revealed a complex inheritance pattern, with both vertical and horizontal transfers. Finally, we reconstructed the evolutionary history of S516 nucleolar group I introns from insertion of mobile-type introns at unoccupied cognate sites, through homing endonuclease gene degradation and loss, and finally to the complete loss of introns. We conclude that myxomycete S516 introns represent a family of genetic elements with surprisingly dynamic structures despite a common function in RNA self-splicing.

Keywords: catalytic introns; homing endonuclease; intron evolution; ribozyme; twintron.

MeSH terms

  • DNA, Ribosomal / genetics
  • Endonucleases / genetics
  • Eukaryota / genetics
  • Introns / genetics
  • Myxomycetes* / genetics
  • Myxomycetes* / metabolism
  • Phylogeny
  • RNA, Catalytic* / genetics
  • RNA, Catalytic* / metabolism

Substances

  • DNA, Ribosomal
  • RNA, Catalytic
  • Endonucleases

Grants and funding

This research received no external funding.