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Review
. 2021 Mar 27;20(2):94-105.
doi: 10.1093/bfgp/elab003.

The non-coding epitranscriptome in cancer

Review

The non-coding epitranscriptome in cancer

Valentina Miano et al. Brief Funct Genomics. .

Abstract

Post-synthesis modification of biomolecules is an efficient way of regulating and optimizing their functions. The human epitranscriptome includes a variety of more than 100 modifications known to exist in all RNA subtypes. Modifications of non-coding RNAs are particularly interesting since they can directly affect their structure, stability, interaction and function. Indeed, non-coding RNAs such as tRNA and rRNA are the most modified RNA species in eukaryotic cells. In the last 20 years, new functions of non-coding RNAs have been discovered and their involvement in human disease, including cancer, became clear. In this review, we will present the evidence connecting modifications of different non-coding RNA subtypes and their role in cancer.

Keywords: RNA epigenetics; RNA methylation; RNA modifications; cancer; epitranscriptomics; non-coding RNA.

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Figures

Figure 1
Figure 1
rRNA and tRNA modifications involved in cancer. Figure depicts RNA modifications (circles) on ribosomal (rRNA, left panel) and transfer RNA (tRNA, right panel) that have been connected to cancer. The enzymes responsible for their deposition are indicated in the balloons. m1acp3Ψ: 1-methyl-3-a-amino-a-carboxyl-propyl pseudouridine; m6A: 6-methyladenosine; m5C: 5-methylcytosine; O-me: 2’O-methylation; Ψ: pseudouridine; m7G: 7-methylguanosine; cm5U: 5- carboxymethyluridine; mcm5U: 5- methoxycarbonylmethyluridine; mcm5s2U: 5-methoxycarbonylmethyl-2-thiouridine.
Figure 2
Figure 2
miRNA, lncRNA and circRNA modifications involved in cancer. Figure depicts RNA modifications (circles) on microRNAs (miRNA, left panel), long non-coding RNAs (lncRNA, top right panel) and circular RNAs (circRNAs, bottom right panel) that have been linked to cancer. The enzymes responsible for their deposition are indicated in the balloons. m7G: 7-methylguanosine; I: inosine; m6A: 6-methyladenosine; P-me: 5’-methylphosphate; 2’-O-me: 2’ O-methylation; m5C: 5- methylcytosine; Ψ: pseudouridine.

References

    1. Roundtree IA, Evans ME, Pan T, et al. Dynamic RNA modifications in gene expression regulation. Cell 2017;169:1187–1200. - PMC - PubMed
    1. Meyer KD, Saletore Y, Zumbo P, et al. Comprehensive analysis of mRNA methylation reveals enrichment in 3′ UTRs and near stop codons. Cell 2012;149:1635–1646. - PMC - PubMed
    1. Dominissini D, Moshitch-Moshkovitz S, Schwartz S, et al. Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq. Nature 2012;485:201–206. - PubMed
    1. Edelheit S, Schwartz S, Mumbach MR, et al. Transcriptome-wide mapping of 5-methylcytidine RNA modifications in bacteria, archaea, and yeast reveals m5C within archaeal mRNAs. PLoS Genet 2013;9:e1003602. - PMC - PubMed
    1. Liu J, Yue Y, Han D, et al. A METTL3-METTL14 complex mediates mammalian nuclear RNA N6-adenosine methylation. Nat Chem Biol 2014;10:93–95. - PMC - PubMed

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