Literature DB >> 30171565

Antisense Oligonucleotide Design and Evaluation of Splice-Modulating Properties Using Cell-Based Assays.

Ralph Slijkerman1,2, Hannie Kremer1,3,4, Erwin van Wijk5,6.   

Abstract

Antisense oligonucleotide (AON)-based splice modulation has been proven to hold great promise as a therapeutic strategy for a number of hereditary conditions. AONs are small modified single-stranded RNA or DNA molecules that are complementary to splice enhancer or silencer target sites. Upon pre-mRNA binding, AONs will prevent or stimulate binding of the spliceosome thereby modulating splicing events. AONs can be designed and applied for different genes and genetic disorders as the specificity depends on their nucleotide sequence. Here we provide a guideline for setting up AON-based splice-modulation experiments by describing a detailed protocol to design and evaluate AONs using a combination of in silico and in vitro analyses.

Entities:  

Keywords:  Antisense oligonucleotides; Genetic therapy; Minigene splice assay; Pre-mRNA; Splice modulation; Splicing

Mesh:

Substances:

Year:  2018        PMID: 30171565     DOI: 10.1007/978-1-4939-8651-4_34

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic ABCA4 Variant c.4539+2001G>A in Stargardt Disease.

Authors:  Alejandro Garanto; Lonneke Duijkers; Tomasz Z Tomkiewicz; Rob W J Collin
Journal:  Genes (Basel)       Date:  2019-06-14       Impact factor: 4.096

2.  AON-based degradation of c.151C>T mutant COCH transcripts associated with dominantly inherited hearing impairment DFNA9.

Authors:  Erik de Vrieze; Jorge Cañas Martín; Jolien Peijnenborg; Aniek Martens; Jaap Oostrik; Simone van den Heuvel; Kornelia Neveling; Ronald Pennings; Hannie Kremer; Erwin van Wijk
Journal:  Mol Ther Nucleic Acids       Date:  2021-03-01       Impact factor: 8.886

3.  Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations.

Authors:  Kalyan Dulla; Ralph Slijkerman; Hester C van Diepen; Silvia Albert; Margo Dona; Wouter Beumer; Janne J Turunen; Hee Lam Chan; Iris A Schulkens; Lars Vorthoren; Cathaline den Besten; Levi Buil; Iris Schmidt; Jiayi Miao; Hanka Venselaar; Jingjing Zang; Stephan C F Neuhauss; Theo Peters; Sanne Broekman; Ronald Pennings; Hannie Kremer; Gerard Platenburg; Peter Adamson; Erik de Vrieze; Erwin van Wijk
Journal:  Mol Ther       Date:  2021-04-23       Impact factor: 12.910

  3 in total

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