| WAI, Htoo A, Eliška SVOBODOVÁ, Natalia Romero HERRERA, Andrew G L DOUGLAS, John W HOLLOWAY, Francisco E BARALLE, Marco BARALLE a Diana BARALLE. Tailored antisense oligonucleotides designed to correct aberrant splicing reveal actionable groups of mutations for rare genetic disorders. EXPERIMENTAL AND MOLECULAR MEDICINE. LONDON: SPRINGERNATURE, 2024, 10 s. ISSN 1226-3613. Dostupné z: https://dx.doi.org/10.1038/s12276-024-01292-1. |
Další formáty:
BibTeX
LaTeX
RIS
@article{2430477,
author = {Wai, Htoo A and Svobodová, Eliška and Herrera, Natalia Romero and Douglas, Andrew G L and Holloway, John W and Baralle, Francisco E and Baralle, Marco and Baralle, Diana},
article_location = {LONDON},
doi = {http://dx.doi.org/10.1038/s12276-024-01292-1},
language = {eng},
issn = {1226-3613},
journal = {EXPERIMENTAL AND MOLECULAR MEDICINE},
title = {Tailored antisense oligonucleotides designed to correct aberrant splicing reveal actionable groups of mutations for rare genetic disorders},
url = {https://www.nature.com/articles/s12276-024-01292-1},
year = {2024}
}
TY - JOUR
ID - 2430477
AU - Wai, Htoo A - Svobodová, Eliška - Herrera, Natalia Romero - Douglas, Andrew G L - Holloway, John W - Baralle, Francisco E - Baralle, Marco - Baralle, Diana
PY - 2024
TI - Tailored antisense oligonucleotides designed to correct aberrant splicing reveal actionable groups of mutations for rare genetic disorders
JF - EXPERIMENTAL AND MOLECULAR MEDICINE
PB - SPRINGERNATURE
SN - 12263613
UR - https://www.nature.com/articles/s12276-024-01292-1
N2 - Effective translation of rare disease diagnosis knowledge into therapeutic applications is achievable within a reasonable timeframe; where mutations are amenable to current antisense oligonucleotide technology. In our study, we identified five distinct types of abnormal splice-causing mutations in patients with rare genetic disorders and developed a tailored antisense oligonucleotide for each mutation type using phosphorodiamidate morpholino oligomers with or without octa-guanidine dendrimers and 2 '-O-methoxyethyl phosphorothioate. We observed variations in treatment effects and efficiencies, influenced by both the chosen chemistry and the specific nature of the aberrant splicing patterns targeted for correction. Our study demonstrated the successful correction of all five different types of aberrant splicing. Our findings reveal that effective correction of aberrant splicing can depend on altering the chemical composition of oligonucleotides and suggest a fast, efficient, and feasible approach for developing personalized therapeutic interventions for genetic disorders within short time frames.
ER -
WAI, Htoo A, Eliška SVOBODOVÁ, Natalia Romero HERRERA, Andrew G L DOUGLAS, John W HOLLOWAY, Francisco E BARALLE, Marco BARALLE a Diana BARALLE. Tailored antisense oligonucleotides designed to correct aberrant splicing reveal actionable groups of mutations for rare genetic disorders. \textit{EXPERIMENTAL AND MOLECULAR MEDICINE}. LONDON: SPRINGERNATURE, 2024, 10 s. ISSN~1226-3613. Dostupné z: https://dx.doi.org/10.1038/s12276-024-01292-1.
|
