Microexons: discovery, regulation, and function

Identification of microexons. Currently available bioinformatics tools for identifying microexons. (a) Salzberg/GMAP and OLego algorithms: (1) When comparing cDNA sequences (Salzberg/GMAP) or RNA‐Seq reads (OLego) to the reference genome, there will be unmappable insertions in the cDNA/RNA‐Seq reads corresponding to unannotated microexons. (2) These algorithms search for potential matches to these segments at high resolution and evaluate candidate splice sites in the reference genome to identify novel exons. (3) After identification of the microexon, the reads map correctly. (b) VAST‐TOOLS: (1) cDNA libraries are used to build an exon junction database. (2) All possible microexon candidates are enumerated in silico by searching pairs of splice site separated by 3–15 nt within known introns. (3) Read mapping for an RNA‐Seq library of interest is performed against this exon‐microexon‐exon junction database to detect microexons. (c) ATMap: (1) Mapping of RNA‐Seq reads to a reference cDNA database lacking a microexon results in unmappable insertions in the read. (2) ATMap returns to the reference genome to identify splice sites surrounding a region that matches the read. (3) After identification of the microexon, the reads map correctly.

Intron‐ and exon‐definition models. Schematic representation of the two primary models that drive assembly of splicing factors complexes and define the use of the splice sites in different mRNA architectures. The intron definition model is applicable to lower eukaryotes such as yeasts where the length of the intronic regions is rather small. The exon definition model proposes an explanation for more complex splicing regulation in higher eukaryotes due to the complexity of the genome organization and the presence of large intronic areas that are on average ten times longer than coding exons.

Function of microexons. Inclusion of microexons can: (a) cause a frame‐shift leading to premature stop codons and degradation of the mRNA via nonsense‐mediated decay, (b) change protein structure which may in turn modulate protein–protein interactions, and (c) create sites for post‐translational modification of proteins.