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Long noncoding RNA-dependent methylation of nonhistone proteins
Salinee Jantrapirom1,2, Nut Koonrungsesomboon1,3, Hideki Yoshida4
1Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Wiley Interdisciplinary Reviews. RNA
|April 29, 2021
Summary
Long noncoding RNAs (lncRNAs) regulate nonhistone protein methylation by acting as scaffolds for methyltransferases. This lncRNA-mediated methylation impacts cell signaling, gene expression, and is implicated in cancer and neurological disorders.
Area of Science:
- Molecular Biology
- Epigenetics
- RNA Biology
Background:
- Long noncoding RNAs (lncRNAs) are transcripts >200 nucleotides with no coding potential.
- Emerging evidence suggests lncRNAs regulate posttranslational modifications of nonhistone proteins.
- The scope of lncRNA-dependent nonhistone protein methylation remains largely uncharacterized.
Purpose of the Study:
- To systematically review and evaluate the impact of lncRNA-dependent methylation of nonhistone proteins.
- To elucidate the mechanisms by which lncRNAs mediate these modifications.
- To explore the biological relevance of these regulatory networks.
Main Methods:
- Systematic literature review.
- Analysis of lncRNA functions as scaffolds for methyltransferases.
- Evaluation of lncRNA roles in regulating methyltransferase activity and target protein modification.
Main Results:
- lncRNAs function as scaffolds, bringing methyltransferases (MTases) and their nonhistone protein targets together.
- Specific MTases like EZH2, PRMT1/4/5, and SMYD2 are modulated by lncRNAs.
- lncRNAs influence nonhistone protein stability and compartmentalization, affecting cell signaling, gene expression, and RNA processing.
- lncRNAs can also indirectly regulate MTase levels through transcriptional or posttranscriptional control.
Conclusions:
- lncRNA-mediated methylation of nonhistone proteins is a significant regulatory mechanism.
- These regulatory networks involving lncRNAs, MTases, and nonhistone proteins are critically implicated in carcinogenesis and neurological disorders.
- Further research into lncRNA-MTase-protein interactions is warranted to understand their roles in disease.
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