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Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs
RNase H1-dependent antisense oligonucleotides (ASOs) can degrade complementary RNAs in both the nucleus and the cytoplasm. Since cytoplasmic mRNAs are actively engaged in translation, ASO activity may thus be affected by translating ribosomes that scan the mRNAs. Here we show that mRNAs associated w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758896/ https://www.ncbi.nlm.nih.gov/pubmed/29165591 http://dx.doi.org/10.1093/nar/gkx1174 |
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author | Liang, Xue-Hai Nichols, Joshua G Sun, Hong Crooke, Stanley T |
author_facet | Liang, Xue-Hai Nichols, Joshua G Sun, Hong Crooke, Stanley T |
author_sort | Liang, Xue-Hai |
collection | PubMed |
description | RNase H1-dependent antisense oligonucleotides (ASOs) can degrade complementary RNAs in both the nucleus and the cytoplasm. Since cytoplasmic mRNAs are actively engaged in translation, ASO activity may thus be affected by translating ribosomes that scan the mRNAs. Here we show that mRNAs associated with ribosomes can be cleaved using ASOs and that translation can alter ASO activity. Translation inhibition tends to increase ASO activity when targeting the coding regions of efficiently translated mRNAs, but not nuclear non-coding RNAs or less efficiently translated mRNAs. Increasing the level of RNase H1 protein eliminated the enhancing effects of translation inhibition on ASO activity, suggesting that RNase H1 recruitment to ASO/mRNA heteroduplexes is a rate limiting step and that translating ribosomes can inhibit RNase H1 recruitment. Consistently, ASO activity was not increased by translation inhibition when targeting the 3′ UTRs, independent of the translation efficiency of the mRNAs. Contrarily, the activity of 3′ UTR-targeting ASOs tended to be reduced upon translation inhibition, likely due to decreased accessibility. These results indicate that ASO activity can be affected by the translation process, and the findings also provide important information toward helping better ASO drug design. |
format | Online Article Text |
id | pubmed-5758896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57588962018-01-16 Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs Liang, Xue-Hai Nichols, Joshua G Sun, Hong Crooke, Stanley T Nucleic Acids Res Molecular Biology RNase H1-dependent antisense oligonucleotides (ASOs) can degrade complementary RNAs in both the nucleus and the cytoplasm. Since cytoplasmic mRNAs are actively engaged in translation, ASO activity may thus be affected by translating ribosomes that scan the mRNAs. Here we show that mRNAs associated with ribosomes can be cleaved using ASOs and that translation can alter ASO activity. Translation inhibition tends to increase ASO activity when targeting the coding regions of efficiently translated mRNAs, but not nuclear non-coding RNAs or less efficiently translated mRNAs. Increasing the level of RNase H1 protein eliminated the enhancing effects of translation inhibition on ASO activity, suggesting that RNase H1 recruitment to ASO/mRNA heteroduplexes is a rate limiting step and that translating ribosomes can inhibit RNase H1 recruitment. Consistently, ASO activity was not increased by translation inhibition when targeting the 3′ UTRs, independent of the translation efficiency of the mRNAs. Contrarily, the activity of 3′ UTR-targeting ASOs tended to be reduced upon translation inhibition, likely due to decreased accessibility. These results indicate that ASO activity can be affected by the translation process, and the findings also provide important information toward helping better ASO drug design. Oxford University Press 2018-01-09 2017-11-20 /pmc/articles/PMC5758896/ /pubmed/29165591 http://dx.doi.org/10.1093/nar/gkx1174 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Liang, Xue-Hai Nichols, Joshua G Sun, Hong Crooke, Stanley T Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs |
title | Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs |
title_full | Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs |
title_fullStr | Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs |
title_full_unstemmed | Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs |
title_short | Translation can affect the antisense activity of RNase H1-dependent oligonucleotides targeting mRNAs |
title_sort | translation can affect the antisense activity of rnase h1-dependent oligonucleotides targeting mrnas |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758896/ https://www.ncbi.nlm.nih.gov/pubmed/29165591 http://dx.doi.org/10.1093/nar/gkx1174 |
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