Mutational bias and the protein code shape the evolution of splicing enhancers.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32504065.
- Also identified by DOI 10.1038/s41467-020-16673-z and PMC identifier 7275064.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Exonic splicing enhancers (ESEs) are enriched in exons relative to introns and bind splicing activators. This study considers a fundamental question of co-evolution: How did ESE motifs become enriched in exons prior to the evolution of ESE recognition? We hypothesize that the high exon to intron motif ratios necessary for ESE function were created by mutational bias coupled with purifying selection on the protein code. These two forces retain certain coding motifs in exons while passively depleting them from introns. Through the use of simulations, genomic analyses, and high throughput splicing assays, we confirm the key predictions of this hypothesis, including an overlap between protein and splicing information in ESEs. We discuss the implications of mutational bias as an evolutionary driver in other cis-regulatory systems.
Medical subject headings
- Enhancer Elements, Genetic
- Evolution, Molecular
- Exons
- Genome, Human
- RNA Splicing