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RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery

RNA interference is almost always associated with post-transcriptional silencing in the cytoplasm. MicroRNAs (miRNAs) and critical RNAi protein factors like argonaute (AGO) and trinucleotide repeat binding containing 6 protein (TNRC6), however, are also found in cell nuclei, suggesting that nuclear...

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Detalles Bibliográficos
Autores principales: Johnson, Krystal C., Corey, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019369/
https://www.ncbi.nlm.nih.gov/pubmed/36657971
http://dx.doi.org/10.1261/rna.079500.122
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author Johnson, Krystal C.
Corey, David R.
author_facet Johnson, Krystal C.
Corey, David R.
author_sort Johnson, Krystal C.
collection PubMed
description RNA interference is almost always associated with post-transcriptional silencing in the cytoplasm. MicroRNAs (miRNAs) and critical RNAi protein factors like argonaute (AGO) and trinucleotide repeat binding containing 6 protein (TNRC6), however, are also found in cell nuclei, suggesting that nuclear miRNAs may be targets for gene regulation. Designed small duplex RNAs (dsRNAs) can modulate nuclear processes such as transcription and splicing, suggesting that they can also provide leads for therapeutic discovery. The goal of this Perspective is to provide the background on nuclear RNAi necessary to guide discussions on whether nuclear RNAi can play a role in therapeutic development programs.
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spelling pubmed-100193692023-04-01 RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery Johnson, Krystal C. Corey, David R. RNA Perspectives RNA interference is almost always associated with post-transcriptional silencing in the cytoplasm. MicroRNAs (miRNAs) and critical RNAi protein factors like argonaute (AGO) and trinucleotide repeat binding containing 6 protein (TNRC6), however, are also found in cell nuclei, suggesting that nuclear miRNAs may be targets for gene regulation. Designed small duplex RNAs (dsRNAs) can modulate nuclear processes such as transcription and splicing, suggesting that they can also provide leads for therapeutic discovery. The goal of this Perspective is to provide the background on nuclear RNAi necessary to guide discussions on whether nuclear RNAi can play a role in therapeutic development programs. Cold Spring Harbor Laboratory Press 2023-04 /pmc/articles/PMC10019369/ /pubmed/36657971 http://dx.doi.org/10.1261/rna.079500.122 Text en © 2023 Johnson and Corey; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Perspectives
Johnson, Krystal C.
Corey, David R.
RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
title RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
title_full RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
title_fullStr RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
title_full_unstemmed RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
title_short RNAi in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
title_sort rnai in cell nuclei: potential for a new layer of biological regulation and a new strategy for therapeutic discovery
topic Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019369/
https://www.ncbi.nlm.nih.gov/pubmed/36657971
http://dx.doi.org/10.1261/rna.079500.122
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