PUBLICATION

RNA structure replaces the need for U2AF65 in splicing

Authors
Lin, C.L., Taggart, A.J., Lim, K.H., Ferraris, L., Cygan, K.J., Creton, R., Huang, Y.T., Fairbrother, W.G.
ID
ZDB-PUB-151115-1
Date
2016
Source
Genome research   26(1): 12-23 (Journal)
Registered Authors
Creton, Robbert
Keywords
none
MeSH Terms
  • Animals
  • Base Sequence
  • Computational Biology
  • Exons
  • Genes, Reporter
  • Introns
  • Molecular Sequence Data
  • Nuclear Proteins/genetics*
  • Nuclear Proteins/metabolism
  • Nucleic Acid Conformation*
  • Phylogeny
  • RNA Precursors/genetics*
  • RNA Precursors/metabolism
  • RNA Splicing*
  • Ribonucleoproteins/genetics
  • Ribonucleoproteins/metabolism
  • Sequence Analysis, RNA
  • Spliceosomes/metabolism
  • Zebrafish/genetics*
PubMed
26566657 Full text @ Genome Res.
Abstract
RNA secondary structure plays an integral role in catalytic, ribosomal, small nuclear, micro, and transfer RNAs. Discovering a prevalent role for secondary structure in pre-mRNAs has proven more elusive. By utilizing a variety of computational and biochemical approaches, we present evidence for a class of nuclear intron that relies upon secondary structure for correct splicing. These introns are defined by simple repeat expansions of complimentary AC and GT dimers that co-occur at opposite boundaries of an intron to form a bridging structure that enforces correct splice site pairing. Remarkably, this class of intron does not require U2AF65, a core component of the spliceosome, for its processing. Phylogenetic analysis suggests that this mechanism was present in the ancestral vertebrate lineage prior to the divergence of tetrapods from teleosts. While largely lost from land dwelling vertebrates, this class of introns is found in 10% of all zebrafish genes.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping