Cargando…

RNA modifications can affect RNase H1-mediated PS-ASO activity

Phosphorothioate modified antisense oligonucleotides (PS-ASOs) can reduce gene expression through hybridization to target RNAs and subsequent cleavage by RNase H1. Target reduction through this mechanism is influenced by numerous features of the RNA, which modulate PS-ASO binding affinities to the R...

Descripción completa

Detalles Bibliográficos
Autores principales: Doxtader Lacy, Katelyn A., Liang, Xue-hai, Zhang, Lingdi, Crooke, Stanley T.
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/PMC9136273/
https://www.ncbi.nlm.nih.gov/pubmed/35664704
http://dx.doi.org/10.1016/j.omtn.2022.05.024
_version_ 1784714142330912768
author Doxtader Lacy, Katelyn A.
Liang, Xue-hai
Zhang, Lingdi
Crooke, Stanley T.
author_facet Doxtader Lacy, Katelyn A.
Liang, Xue-hai
Zhang, Lingdi
Crooke, Stanley T.
author_sort Doxtader Lacy, Katelyn A.
collection PubMed
description Phosphorothioate modified antisense oligonucleotides (PS-ASOs) can reduce gene expression through hybridization to target RNAs and subsequent cleavage by RNase H1. Target reduction through this mechanism is influenced by numerous features of the RNA, which modulate PS-ASO binding affinities to the RNA target, and how the PS-ASO-RNA hybrid is recognized by RNase H1 for RNA cleavage. Endogenous RNAs are frequently chemically modified, which can regulate intra- and intermolecular interactions of the RNA. The effects of PS-ASO modifications on antisense activity have been well studied; however, much less is known regarding the effects of RNA modifications on PS-ASO hybridization and RNase H1 cleavage activity. Here, we determine the effects of three different RNA modifications on PS-ASO binding and antisense activity in recombinant and cell-based systems. Some RNA modifications can reduce PS-ASO hybridization, the cleavage activity of RNase H1, or both, while other modifications had minimal effects on PS-ASO function. In addition to these direct effects, RNA modifications can also change the RNA structure, which may affect PS-ASO accessibility in a cellular context. Our results elucidate the effects of three prevalent RNA modifications on PS-ASO-mediated RNase H1 cleavage activity, and such findings will help improve PS-ASO target site selection.
format Online
Article
Text
id pubmed-9136273
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society of Gene & Cell Therapy
record_format MEDLINE/PubMed
spelling pubmed-91362732022-06-04 RNA modifications can affect RNase H1-mediated PS-ASO activity Doxtader Lacy, Katelyn A. Liang, Xue-hai Zhang, Lingdi Crooke, Stanley T. Mol Ther Nucleic Acids Original Article Phosphorothioate modified antisense oligonucleotides (PS-ASOs) can reduce gene expression through hybridization to target RNAs and subsequent cleavage by RNase H1. Target reduction through this mechanism is influenced by numerous features of the RNA, which modulate PS-ASO binding affinities to the RNA target, and how the PS-ASO-RNA hybrid is recognized by RNase H1 for RNA cleavage. Endogenous RNAs are frequently chemically modified, which can regulate intra- and intermolecular interactions of the RNA. The effects of PS-ASO modifications on antisense activity have been well studied; however, much less is known regarding the effects of RNA modifications on PS-ASO hybridization and RNase H1 cleavage activity. Here, we determine the effects of three different RNA modifications on PS-ASO binding and antisense activity in recombinant and cell-based systems. Some RNA modifications can reduce PS-ASO hybridization, the cleavage activity of RNase H1, or both, while other modifications had minimal effects on PS-ASO function. In addition to these direct effects, RNA modifications can also change the RNA structure, which may affect PS-ASO accessibility in a cellular context. Our results elucidate the effects of three prevalent RNA modifications on PS-ASO-mediated RNase H1 cleavage activity, and such findings will help improve PS-ASO target site selection. American Society of Gene & Cell Therapy 2022-05-11 /pmc/articles/PMC9136273/ /pubmed/35664704 http://dx.doi.org/10.1016/j.omtn.2022.05.024 Text en © 2022 Ionis Pharmaceuticals 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
Doxtader Lacy, Katelyn A.
Liang, Xue-hai
Zhang, Lingdi
Crooke, Stanley T.
RNA modifications can affect RNase H1-mediated PS-ASO activity
title RNA modifications can affect RNase H1-mediated PS-ASO activity
title_full RNA modifications can affect RNase H1-mediated PS-ASO activity
title_fullStr RNA modifications can affect RNase H1-mediated PS-ASO activity
title_full_unstemmed RNA modifications can affect RNase H1-mediated PS-ASO activity
title_short RNA modifications can affect RNase H1-mediated PS-ASO activity
title_sort rna modifications can affect rnase h1-mediated ps-aso activity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136273/
https://www.ncbi.nlm.nih.gov/pubmed/35664704
http://dx.doi.org/10.1016/j.omtn.2022.05.024
work_keys_str_mv AT doxtaderlacykatelyna rnamodificationscanaffectrnaseh1mediatedpsasoactivity
AT liangxuehai rnamodificationscanaffectrnaseh1mediatedpsasoactivity
AT zhanglingdi rnamodificationscanaffectrnaseh1mediatedpsasoactivity
AT crookestanleyt rnamodificationscanaffectrnaseh1mediatedpsasoactivity