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Exploring the methyl-verse: Dynamic interplay of epigenome and m6A epitranscriptome
Katerina-Marina Pilala1, Konstantina Panoutsopoulou1, Maria-Alexandra Papadimitriou1
1Department of Biochemistry and Molecular Biology, Faculty of Biology, National and Kapodistrian University of Athens, Athens, Greece.
RNA methylation (m6A) and DNA methylation crosstalk fine-tune gene expression. This review explores m6A circuits, epigenetic interactions, and novel CRISPR-based RNA therapeutics for cancer.
Area of Science:
- Molecular Biology
- Epigenetics
- RNA Biology
Background:
- Epigenetic and epitranscriptomic modifications regulate gene expression but are often studied in isolation.
- Emerging research reveals interplay between N6-methyladenosine (m6A) RNA methylation and epigenetic mechanisms.
- This interaction forms feedback circuits influencing gene expression and cellular homeostasis.
Purpose of the Study:
- To review the coordinated circuits of m6A with DNA methylation, chromatin, and non-coding RNAs.
- To elucidate these interactions in normal physiology and carcinogenesis.
- To summarize advancements in CRISPR-based platforms for m6A epitranscriptome editing.
Main Methods:
- Literature review of studies on m6A RNA methylation.
- Analysis of m6A interactions with DNA methylation and histone modifications.
- Review of CRISPR-dCas engineering platforms for m6A editing.
Main Results:
- m6A RNA methylation interacts with DNA methylation and histone modifications, shaping transcription and translation.
- m6A also modulates non-coding RNA functions.
- m6A acts as a checkpoint linking epigenetic and epitranscriptomic layers.
Conclusions:
- m6A-mediated crosstalk with epigenetic factors provides multilayered control of gene expression.
- Understanding these networks is crucial for normal physiology and cancer.
- CRISPR-dCas technologies offer precise transcript-specific m6A editing for therapeutic development.
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