Genome-wide evolution of wobble base-pairing nucleotides of branchpoint motifs with increasing organismal complexity

RNA Biol. 2020 Mar;17(3):311-324. doi: 10.1080/15476286.2019.1697548. Epub 2019 Dec 19.

Abstract

How have the branchpoint motifs evolved in organisms of different complexity? Here we identified and examined the consensus motifs (R1C2T3R4A5Y6, R: A or G, Y: C or T) of 898 fungal genomes. In Ascomycota unicellular yeasts, the G4/A4 ratio is mostly (98%) below 0.125 but increases sharply in multicellular species by about 40 times on average, and in the more complex Basidiomycota, it increases further by about 7 times. The global G4 increase is consistent with A4 to G4 transitions in evolution. Of the G4/A4-interacting amino acids of the branchpoint binding protein MSL5 (SF1) and the HSH155 (SF3B1), as well as the 5' splice sites (SS) and U2 snRNA genes, the 5' SS G3/A3 co-vary with the G4 to some extent. However, corresponding increase of the G4-complementary GCAGTA-U2 gene is rare, suggesting wobble-base pairing between the G4-containing branchpoint motif and GTAGTA-U2 in most of these species. Interestingly, the G4/A4 ratio correlates well with the abundance of alternative splicing in the two phyla, and G4 enriched significantly at the alternative 3' SS of genes in RNA metabolism, kinases and membrane proteins. Similar wobble nucleotides also enriched at the 3' SS of multicellular fungi with only thousands of protein-coding genes. Thus, branchpoint motifs have evolved U2-complementarity in unicellular Ascomycota yeasts, but have gradually gained more wobble base-pairing nucleotides in fungi of higher complexity, likely to destabilize branchpoint motif-U2 interaction and/or branchpoint A protrusion for alternative splicing. This implies an important role of relaxing the branchpoint signals in the multicellularity and further complexity of fungi.

Keywords: 3ʹ splice site; branchpoint; fungi; intron; species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Ascomycota / cytology
  • Ascomycota / genetics*
  • Base Pairing*
  • Basidiomycota / genetics
  • Cytidine / genetics
  • Evolution, Molecular
  • Fungal Proteins / genetics
  • Genome, Fungal*
  • Nucleotide Motifs*
  • RNA Splice Sites*
  • RNA, Small Nuclear

Substances

  • Fungal Proteins
  • RNA Splice Sites
  • RNA, Small Nuclear
  • U2 small nuclear RNA
  • Cytidine

Grants and funding

This work is supported by the Natural Sciences and Engineering Research Council of Canada (NSERC, RGPIN/6004-2016) and a Manitoba Research Chair fund to J.X. H.N. is supported in part by a graduate scholarship from the Research Manitoba, and U.D. by a UMGF scholarship.