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Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes
BACKGROUND: Canonical nonsense-mediated decay (NMD) is an important splicing-dependent process for mRNA surveillance in mammals. However, processed pseudogenes are not able to trigger NMD due to their lack of introns. It is largely unknown whether they have evolved other surveillance mechanisms. RES...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201931/ https://www.ncbi.nlm.nih.gov/pubmed/34120636 http://dx.doi.org/10.1186/s13059-021-02402-2 |
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author | Tan, Liqiang Cheng, Weisheng Liu, Fang Wang, Dan Ohtan Wu, Linwei Cao, Nan Wang, Jinkai |
author_facet | Tan, Liqiang Cheng, Weisheng Liu, Fang Wang, Dan Ohtan Wu, Linwei Cao, Nan Wang, Jinkai |
author_sort | Tan, Liqiang |
collection | PubMed |
description | BACKGROUND: Canonical nonsense-mediated decay (NMD) is an important splicing-dependent process for mRNA surveillance in mammals. However, processed pseudogenes are not able to trigger NMD due to their lack of introns. It is largely unknown whether they have evolved other surveillance mechanisms. RESULTS: Here, we find that the RNAs of pseudogenes, especially processed pseudogenes, have dramatically higher m(6)A levels than their cognate protein-coding genes, associated with de novo m(6)A peaks and motifs in human cells. Furthermore, pseudogenes have rapidly accumulated m(6)A motifs during evolution. The m(6)A sites of pseudogenes are evolutionarily younger than neutral sites and their m(6)A levels are increasing, supporting the idea that m(6)A on the RNAs of pseudogenes is under positive selection. We then find that the m(6)A RNA modification of processed, rather than unprocessed, pseudogenes promotes cytosolic RNA degradation and attenuates interference with the RNAs of their cognate protein-coding genes. We experimentally validate the m(6)A RNA modification of two processed pseudogenes, DSTNP2 and NAP1L4P1, which promotes the RNA degradation of both pseudogenes and their cognate protein-coding genes DSTN and NAP1L4. In addition, the m(6)A of DSTNP2 regulation of DSTN is partially dependent on the miRNA miR-362-5p. CONCLUSIONS: Our discovery reveals a novel evolutionary role of m(6)A RNA modification in cleaning up the unnecessary processed pseudogene transcripts to attenuate their interference with the regulatory network of protein-coding genes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02402-2. |
format | Online Article Text |
id | pubmed-8201931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82019312021-06-16 Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes Tan, Liqiang Cheng, Weisheng Liu, Fang Wang, Dan Ohtan Wu, Linwei Cao, Nan Wang, Jinkai Genome Biol Research BACKGROUND: Canonical nonsense-mediated decay (NMD) is an important splicing-dependent process for mRNA surveillance in mammals. However, processed pseudogenes are not able to trigger NMD due to their lack of introns. It is largely unknown whether they have evolved other surveillance mechanisms. RESULTS: Here, we find that the RNAs of pseudogenes, especially processed pseudogenes, have dramatically higher m(6)A levels than their cognate protein-coding genes, associated with de novo m(6)A peaks and motifs in human cells. Furthermore, pseudogenes have rapidly accumulated m(6)A motifs during evolution. The m(6)A sites of pseudogenes are evolutionarily younger than neutral sites and their m(6)A levels are increasing, supporting the idea that m(6)A on the RNAs of pseudogenes is under positive selection. We then find that the m(6)A RNA modification of processed, rather than unprocessed, pseudogenes promotes cytosolic RNA degradation and attenuates interference with the RNAs of their cognate protein-coding genes. We experimentally validate the m(6)A RNA modification of two processed pseudogenes, DSTNP2 and NAP1L4P1, which promotes the RNA degradation of both pseudogenes and their cognate protein-coding genes DSTN and NAP1L4. In addition, the m(6)A of DSTNP2 regulation of DSTN is partially dependent on the miRNA miR-362-5p. CONCLUSIONS: Our discovery reveals a novel evolutionary role of m(6)A RNA modification in cleaning up the unnecessary processed pseudogene transcripts to attenuate their interference with the regulatory network of protein-coding genes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02402-2. BioMed Central 2021-06-13 /pmc/articles/PMC8201931/ /pubmed/34120636 http://dx.doi.org/10.1186/s13059-021-02402-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Tan, Liqiang Cheng, Weisheng Liu, Fang Wang, Dan Ohtan Wu, Linwei Cao, Nan Wang, Jinkai Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes |
title | Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes |
title_full | Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes |
title_fullStr | Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes |
title_full_unstemmed | Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes |
title_short | Positive natural selection of N6-methyladenosine on the RNAs of processed pseudogenes |
title_sort | positive natural selection of n6-methyladenosine on the rnas of processed pseudogenes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201931/ https://www.ncbi.nlm.nih.gov/pubmed/34120636 http://dx.doi.org/10.1186/s13059-021-02402-2 |
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