Peptidic tools applied to redirect alternative splicing events

Peptides. 2015 May:67:1-11. doi: 10.1016/j.peptides.2015.02.006. Epub 2015 Mar 6.

Abstract

Peptides are versatile and attractive biomolecules that can be applied to modulate genetic mechanisms like alternative splicing. In this process, a single transcript yields different mature RNAs leading to the production of protein isoforms with diverse or even antagonistic functions. During splicing events, errors can be caused either by mutations present in the genome or by defects or imbalances in regulatory protein factors. In any case, defects in alternative splicing have been related to several genetic diseases including muscular dystrophy, Alzheimer's disease and cancer from almost every origin. One of the most effective approaches to redirect alternative splicing events has been to attach cell-penetrating peptides to oligonucleotides that can modulate a single splicing event and restore correct gene expression. Here, we summarize how natural existing and bioengineered peptides have been applied over the last few years to regulate alternative splicing and genetic expression. Under different genetic and cellular backgrounds, peptides have been shown to function as potent vehicles for splice correction, and their therapeutic benefits have reached clinical trials and patenting stages, emphasizing the use of regulatory peptides as an exciting therapeutic tool for the treatment of different genetic diseases.

Keywords: Cell-penetrating peptide; Mutations; Peptide nucleic acid; Splicing; mRNA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alternative Splicing*
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell-Penetrating Peptides / metabolism*
  • Cell-Penetrating Peptides / pharmacology
  • Genetic Diseases, Inborn / therapy
  • Humans
  • Molecular Sequence Data
  • Peptide Nucleic Acids / metabolism*
  • Peptide Nucleic Acids / pharmacology
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Transfection*

Substances

  • Cell-Penetrating Peptides
  • Peptide Nucleic Acids
  • Protein Isoforms