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N 6 -Methyladenosine landscape of glioma stem-like cells: METTL3 is essential for the expression of actively transcribed genes and sustenance of the oncogenic signaling

Visvanathan, A and Patil, V and Abdulla, S and Hoheisel, JD and Somasundaram, K (2019) N 6 -Methyladenosine landscape of glioma stem-like cells: METTL3 is essential for the expression of actively transcribed genes and sustenance of the oncogenic signaling. In: Genes, 10 (2).

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Official URL: https://doi.org/10.3390/genes10020141

Abstract

Despite recent advances in N 6 -methyladenosine (m 6 A) biology, the regulation of crucial RNA processing steps by the RNA methyltransferase-like 3 (METTL3) in glioma stem-like cells (GSCs) remains obscure. An integrated analysis of m 6 A-RIP (RNA immunoprecipitation) and total RNA-Seq of METTL3-silenced GSCs identified that m 6 A modification in GSCs is principally carried out by METTL3. The m 6 A-modified transcripts showed higher abundance compared to non-modified transcripts. Further, we showed that the METTL3 is essential for the expression of GSC-specific actively transcribed genes. Silencing METTL3 resulted in the elevation of several aberrant alternative splicing events. We also found that putative m 6 A reader proteins play a key role in the RNA stabilization function of METTL3. METTL3 altered A-to-I and C-to-U RNA editing events by differentially regulating RNA editing enzymes ADAR and APOBEC3A. Similar to protein-coding genes, lincRNAs (long intergenic non-coding RNAs) with m 6 A marks showed METTL3-dependent high expression. m 6 A modification of 30UTRs appeared to result in a conformation-dependent hindrance to miRNA binding to their targets. The integrated analysis of the m 6 A regulome in METTL3-silenced GSCs showed global disruption in tumorigenic pathways that are indispensable for GSC maintenance and glioma progression. We conclude that METTL3 plays a vital role in many steps of RNA processing and orchestrates successful execution of oncogenic pathways in GSCs. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.

Item Type: Journal Article
Publication: Genes
Publisher: MDPI AG
Additional Information: cited By 0
Department/Centre: Division of Biological Sciences > Microbiology & Cell Biology
Date Deposited: 24 Apr 2019 05:31
Last Modified: 23 Sep 2022 05:59
URI: https://eprints.iisc.ac.in/id/eprint/62164

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