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Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs

Nonsense mutations or premature termination codons (PTCs) comprise ∼11% of all genetic lesions, which result in over 7,000 distinct genetic diseases. Due to their outsized impact on human health, considerable effort has been made to find therapies for nonsense-associated diseases. Suppressor tRNAs h...

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Autores principales: Ko, Wooree, Porter, Joseph J., Sipple, Matthew T., Edwards, Katherine M., Lueck, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126842/
https://www.ncbi.nlm.nih.gov/pubmed/35664697
http://dx.doi.org/10.1016/j.omtn.2022.04.033
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author Ko, Wooree
Porter, Joseph J.
Sipple, Matthew T.
Edwards, Katherine M.
Lueck, John D.
author_facet Ko, Wooree
Porter, Joseph J.
Sipple, Matthew T.
Edwards, Katherine M.
Lueck, John D.
author_sort Ko, Wooree
collection PubMed
description Nonsense mutations or premature termination codons (PTCs) comprise ∼11% of all genetic lesions, which result in over 7,000 distinct genetic diseases. Due to their outsized impact on human health, considerable effort has been made to find therapies for nonsense-associated diseases. Suppressor tRNAs have long been identified as a possible therapeutic for nonsense-associated diseases; however, their ability to inhibit nonsense-mediated mRNA decay (NMD) and support significant protein translation from endogenous transcripts has not been determined in mammalian cells. Here, we investigated the ability of anticodon edited (ACE)-tRNAs to suppress cystic fibrosis (CF) causing PTCs in the cystic fibrosis transmembrane regulator (CFTR) gene in gene-edited immortalized human bronchial epithelial (16HBEge) cells. Delivery of ACE-tRNAs to 16HBEge cells harboring three common CF mutations G542XUGA-, R1162XUGA-, and W1282XUGA-CFTR PTCs significantly inhibited NMD and rescued endogenous mRNA expression. Furthermore, delivery of our highly active leucine-encoding ACE-tRNA resulted in rescue of W1282X-CFTR channel function to levels that significantly exceed the necessary CFTR channel function for therapeutic relevance. This study establishes the ACE-tRNA approach as a potential standalone therapeutic for nonsense-associated diseases due to its ability to rescue both mRNA and full-length protein expression from PTC-containing endogenous genes.
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spelling pubmed-91268422022-06-04 Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs Ko, Wooree Porter, Joseph J. Sipple, Matthew T. Edwards, Katherine M. Lueck, John D. Mol Ther Nucleic Acids Original Article Nonsense mutations or premature termination codons (PTCs) comprise ∼11% of all genetic lesions, which result in over 7,000 distinct genetic diseases. Due to their outsized impact on human health, considerable effort has been made to find therapies for nonsense-associated diseases. Suppressor tRNAs have long been identified as a possible therapeutic for nonsense-associated diseases; however, their ability to inhibit nonsense-mediated mRNA decay (NMD) and support significant protein translation from endogenous transcripts has not been determined in mammalian cells. Here, we investigated the ability of anticodon edited (ACE)-tRNAs to suppress cystic fibrosis (CF) causing PTCs in the cystic fibrosis transmembrane regulator (CFTR) gene in gene-edited immortalized human bronchial epithelial (16HBEge) cells. Delivery of ACE-tRNAs to 16HBEge cells harboring three common CF mutations G542XUGA-, R1162XUGA-, and W1282XUGA-CFTR PTCs significantly inhibited NMD and rescued endogenous mRNA expression. Furthermore, delivery of our highly active leucine-encoding ACE-tRNA resulted in rescue of W1282X-CFTR channel function to levels that significantly exceed the necessary CFTR channel function for therapeutic relevance. This study establishes the ACE-tRNA approach as a potential standalone therapeutic for nonsense-associated diseases due to its ability to rescue both mRNA and full-length protein expression from PTC-containing endogenous genes. American Society of Gene & Cell Therapy 2022-05-04 /pmc/articles/PMC9126842/ /pubmed/35664697 http://dx.doi.org/10.1016/j.omtn.2022.04.033 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Ko, Wooree
Porter, Joseph J.
Sipple, Matthew T.
Edwards, Katherine M.
Lueck, John D.
Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs
title Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs
title_full Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs
title_fullStr Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs
title_full_unstemmed Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs
title_short Efficient suppression of endogenous CFTR nonsense mutations using anticodon-engineered transfer RNAs
title_sort efficient suppression of endogenous cftr nonsense mutations using anticodon-engineered transfer rnas
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126842/
https://www.ncbi.nlm.nih.gov/pubmed/35664697
http://dx.doi.org/10.1016/j.omtn.2022.04.033
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