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Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation

The presence and absence of RNA modifications regulates RNA metabolism by modulating the binding of writer, reader, and eraser proteins. For 5-methylcytosine (m(5)C) however, it is largely unknown how it recruits or repels RNA-binding proteins. Here, we decipher the consequences of m(5)C deposition...

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Autores principales: Sajini, Abdulrahim A., Choudhury, Nila Roy, Wagner, Rebecca E., Bornelöv, Susanne, Selmi, Tommaso, Spanos, Christos, Dietmann, Sabine, Rappsilber, Juri, Michlewski, Gracjan, Frye, Michaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560067/
https://www.ncbi.nlm.nih.gov/pubmed/31186410
http://dx.doi.org/10.1038/s41467-019-10020-7
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author Sajini, Abdulrahim A.
Choudhury, Nila Roy
Wagner, Rebecca E.
Bornelöv, Susanne
Selmi, Tommaso
Spanos, Christos
Dietmann, Sabine
Rappsilber, Juri
Michlewski, Gracjan
Frye, Michaela
author_facet Sajini, Abdulrahim A.
Choudhury, Nila Roy
Wagner, Rebecca E.
Bornelöv, Susanne
Selmi, Tommaso
Spanos, Christos
Dietmann, Sabine
Rappsilber, Juri
Michlewski, Gracjan
Frye, Michaela
author_sort Sajini, Abdulrahim A.
collection PubMed
description The presence and absence of RNA modifications regulates RNA metabolism by modulating the binding of writer, reader, and eraser proteins. For 5-methylcytosine (m(5)C) however, it is largely unknown how it recruits or repels RNA-binding proteins. Here, we decipher the consequences of m(5)C deposition into the abundant non-coding vault RNA VTRNA1.1. Methylation of cytosine 69 in VTRNA1.1 occurs frequently in human cells, is exclusively mediated by NSUN2, and determines the processing of VTRNA1.1 into small-vault RNAs (svRNAs). We identify the serine/arginine rich splicing factor 2 (SRSF2) as a novel VTRNA1.1-binding protein that counteracts VTRNA1.1 processing by binding the non-methylated form with higher affinity. Both NSUN2 and SRSF2 orchestrate the production of distinct svRNAs. Finally, we discover a functional role of svRNAs in regulating the epidermal differentiation programme. Thus, our data reveal a direct role for m(5)C in the processing of VTRNA1.1 that involves SRSF2 and is crucial for efficient cellular differentiation.
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spelling pubmed-65600672019-06-21 Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation Sajini, Abdulrahim A. Choudhury, Nila Roy Wagner, Rebecca E. Bornelöv, Susanne Selmi, Tommaso Spanos, Christos Dietmann, Sabine Rappsilber, Juri Michlewski, Gracjan Frye, Michaela Nat Commun Article The presence and absence of RNA modifications regulates RNA metabolism by modulating the binding of writer, reader, and eraser proteins. For 5-methylcytosine (m(5)C) however, it is largely unknown how it recruits or repels RNA-binding proteins. Here, we decipher the consequences of m(5)C deposition into the abundant non-coding vault RNA VTRNA1.1. Methylation of cytosine 69 in VTRNA1.1 occurs frequently in human cells, is exclusively mediated by NSUN2, and determines the processing of VTRNA1.1 into small-vault RNAs (svRNAs). We identify the serine/arginine rich splicing factor 2 (SRSF2) as a novel VTRNA1.1-binding protein that counteracts VTRNA1.1 processing by binding the non-methylated form with higher affinity. Both NSUN2 and SRSF2 orchestrate the production of distinct svRNAs. Finally, we discover a functional role of svRNAs in regulating the epidermal differentiation programme. Thus, our data reveal a direct role for m(5)C in the processing of VTRNA1.1 that involves SRSF2 and is crucial for efficient cellular differentiation. Nature Publishing Group UK 2019-06-11 /pmc/articles/PMC6560067/ /pubmed/31186410 http://dx.doi.org/10.1038/s41467-019-10020-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sajini, Abdulrahim A.
Choudhury, Nila Roy
Wagner, Rebecca E.
Bornelöv, Susanne
Selmi, Tommaso
Spanos, Christos
Dietmann, Sabine
Rappsilber, Juri
Michlewski, Gracjan
Frye, Michaela
Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation
title Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation
title_full Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation
title_fullStr Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation
title_full_unstemmed Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation
title_short Loss of 5-methylcytosine alters the biogenesis of vault-derived small RNAs to coordinate epidermal differentiation
title_sort loss of 5-methylcytosine alters the biogenesis of vault-derived small rnas to coordinate epidermal differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560067/
https://www.ncbi.nlm.nih.gov/pubmed/31186410
http://dx.doi.org/10.1038/s41467-019-10020-7
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