mRNA methylation in cell senescence
Cellular senescence, a developmental program central to normal aging and aging pathologies, is robustly regulated at the post‐transcriptional level. This regulation involves the interaction of RNA‐binding proteins and noncoding RNAs with senescence‐associated messenger RNAs (mRNAs). There is increas...
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| Vydáno v: | Wiley interdisciplinary reviews. RNA Ročník 10; číslo 6; s. e1547 - n/a |
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| Hlavní autoři: | , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Hoboken, USA
John Wiley & Sons, Inc
01.11.2019
Wiley Subscription Services, Inc |
| Témata: | |
| ISSN: | 1757-7004, 1757-7012, 1757-7012 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | Cellular senescence, a developmental program central to normal aging and aging pathologies, is robustly regulated at the post‐transcriptional level. This regulation involves the interaction of RNA‐binding proteins and noncoding RNAs with senescence‐associated messenger RNAs (mRNAs). There is increasing evidence that these associations are modulated by chemical modifications of specific mRNA nucleotides which can enhance or reduce the binding of regulatory factors. Recent technological advances in mass spectrometry, next‐generation sequencing, and genome mapping have improved markedly the detection of mRNA modifications. Given the rising interest in the epitranscriptomic control of gene expression in aging, we discuss our incipient understanding of the chemical mRNA modifications, specifically m6A and m5C, that influence cellular senescence.
This article is categorized under:
RNA Export and Localization > RNA Localization
RNA Processing > RNA Editing and Modification
Main regulatory modifications reported in mRNAs encoding senescence‐associated proteins, m6A and m5C. Each modification can promote (green) or repress (purple) protein expression from the respective mRNAs. |
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| Bibliografie: | Funding information National Institute on Aging, NIH, Grant/Award Number: AG000393‐11 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 Gabriel Casella and Dimitrios Tsitsipatis contributed equally to this study. |
| ISSN: | 1757-7004 1757-7012 1757-7012 |
| DOI: | 10.1002/wrna.1547 |