Unknown

Dataset Information

0

Biological impact of mutually exclusive exon switching.


ABSTRACT: Alternative splicing can expand the diversity of proteomes. Homologous mutually exclusive exons (MXEs) originate from the same ancestral exon and result in polypeptides with similar structural properties but altered sequence. Why would some genes switch homologous exons and what are their biological impact? Here, we analyse the extent of sequence, structural and functional variability in MXEs and report the first large scale, structure-based analysis of the biological impact of MXE events from different genomes. MXE-specific residues tend to map to single domains, are highly enriched in surface exposed residues and cluster at or near protein functional sites. Thus, MXE events are likely to maintain the protein fold, but alter specificity and selectivity of protein function. This comprehensive resource of MXE events and their annotations is available at: http://gene3d.biochem.ucl.ac.uk/mxemod/. These findings highlight how small, but significant changes at critical positions on a protein surface are exploited in evolution to alter function.

SUBMITTER: Lam SD 

PROVIDER: S-EPMC7954323 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Biological impact of mutually exclusive exon switching.

Lam Su Datt SD   Babu M Madan MM   Lees Jonathan J   Orengo Christine A CA  

PLoS computational biology 20210302 3


Alternative splicing can expand the diversity of proteomes. Homologous mutually exclusive exons (MXEs) originate from the same ancestral exon and result in polypeptides with similar structural properties but altered sequence. Why would some genes switch homologous exons and what are their biological impact? Here, we analyse the extent of sequence, structural and functional variability in MXEs and report the first large scale, structure-based analysis of the biological impact of MXE events from d  ...[more]

Similar Datasets

2018-11-19 | GSE115977 | GEO
| S-EPMC7573352 | biostudies-literature
| S-EPMC3228551 | biostudies-literature
| S-EPMC2921853 | biostudies-literature
| S-EPMC2216695 | biostudies-literature
| S-EPMC7551865 | biostudies-literature
| PRJNA476616 | ENA
| S-EPMC5740500 | biostudies-literature
| S-EPMC6282950 | biostudies-literature
| S-EPMC3050534 | biostudies-literature