Related Experiment Video
Updated: Aug 11, 2026

07:02
Evaluation of Exon Inclusion Induced by Splice Switching Antisense Oligonucleotides in SMA Patient Fibroblasts
Published on: May 11, 2018
An antisense antidote to oncogenic poison exons
René M Arvola1, Guramrit Singh2
1Department of Molecular Genetics, Center for RNA Biology, The Ohio State University, Columbus, Ohio 43210, USA.
Genes & Development
|August 4, 2026
Summary
Mutant SRSF2 splicing factors cause cancer by including poison exons in EZH2 mRNA. Researchers identified an antisense oligonucleotide to block these exons, restoring EZH2 function and rescuing blood cell defects.
Area of Science:
- Molecular biology
- Cancer genetics
- RNA splicing
Background:
- Splicing factors, like SRSF2, are often mutated in myeloid cancers.
- These mutations lead to aberrant RNA splicing, affecting tumor suppressor gene expression.
- In SRSF2-mutated cancers, a specific oncogenic event involves the inclusion of a poison exon in EZH2 mRNA.
Purpose of the Study:
- To elucidate the mechanism by which mutant SRSF2 binding leads to poison exon inclusion in EZH2.
- To identify therapeutic strategies targeting this oncogenic splicing event.
- To evaluate the potential of antisense oligonucleotides in restoring EZH2 function.
Main Methods:
- Investigated the binding of mutant SRSF2 to the poison exon.
- Utilized antisense oligonucleotides to target and repress the poison exon.
- Assessed the restoration of EZH2 function and rescue of hematopoietic defects.
Main Results:
- Defined the mechanism of mutant SRSF2-mediated poison exon inclusion.
- Identified an antisense oligonucleotide that effectively represses the poison exon.
- Demonstrated that this repression restores EZH2 function and rescues hematopoietic defects in preclinical models.
Conclusions:
- Mutant SRSF2 binding to poison exons is a key oncogenic event in myeloid cancers.
- Targeting poison exons with antisense oligonucleotides is a promising therapeutic strategy.
- Restoring EZH2 function via poison exon repression offers a novel approach to cancer treatment.
Related Concept Videos
Antidotes
Antidotes are medicinal substances used to counteract the harmful effects of toxins or drugs in the body. They function in various ways, each uniquely designed to combat specific toxic compounds.
Specific antidotes operate by inhibiting the enzymes that control biochemical pathways, reducing the production of harmful metabolites.
An example of an antidote is atropine, which counteracts the detrimental effects of cholinesterase inhibitors. It achieves this by deactivating muscarinic receptors,...
Specific antidotes operate by inhibiting the enzymes that control biochemical pathways, reducing the production of harmful metabolites.
An example of an antidote is atropine, which counteracts the detrimental effects of cholinesterase inhibitors. It achieves this by deactivating muscarinic receptors,...
Nonsense-mediated mRNA Decay
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Nonsense-mediated mRNA Decay
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Experimental RNAi
RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
Exon Recombination
The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes.
Exon shuffling follows “splice frame rules.” Each exon has three reading...
Exon shuffling follows “splice frame rules.” Each exon has three reading...
RNA Interference
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
