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FunDMDeep-m 6 A: identification and prioritization of functional differential m 6 A methylation genes.

Authors :
Zhang, Song-Yao
Zhang, Shao-Wu
Fan, Xiao-Nan
Zhang, Teng
Meng, Jia
Huang, Yufei
Source :
Bioinformatics; Jul2019, Vol. 35 Issue 14, pi90-i98, 9p
Publication Year :
2019

Abstract

Motivation As the most abundant mammalian mRNA methylation, N <superscript>6</superscript>-methyladenosine (m<superscript>6</superscript>A) exists in >25% of human mRNAs and is involved in regulating many different aspects of mRNA metabolism, stem cell differentiation and diseases like cancer. However, our current knowledge about dynamic changes of m<superscript>6</superscript>A levels and how the change of m<superscript>6</superscript>A levels for a specific gene can play a role in certain biological processes like stem cell differentiation and diseases like cancer is largely elusive. Results To address this, we propose in this paper FunDMDeep-m<superscript>6</superscript>A a novel pipeline for identifying context-specific (e.g. disease versus normal, differentiated cells versus stem cells or gene knockdown cells versus wild-type cells) m<superscript>6</superscript>A-mediated functional genes. FunDMDeep-m<superscript>6</superscript>A includes, at the first step, DMDeep-m<superscript>6</superscript>A a novel method based on a deep learning model and a statistical test for identifying differential m<superscript>6</superscript>A methylation (DmM) sites from MeRIP-Seq data at a single-base resolution. FunDMDeep-m<superscript>6</superscript>A then identifies and prioritizes functional DmM genes (FDmMGenes) by combing the DmM genes (DmMGenes) with differential expression analysis using a network-based method. This proposed network method includes a novel m<superscript>6</superscript>A-signaling bridge (MSB) score to quantify the functional significance of DmMGenes by assessing functional interaction of DmMGenes with their signaling pathways using a heat diffusion process in protein-protein interaction (PPI) networks. The test results on 4 context-specific MeRIP-Seq datasets showed that FunDMDeep-m<superscript>6</superscript>A can identify more context-specific and functionally significant FDmMGenes than m<superscript>6</superscript>A-Driver. The functional enrichment analysis of these genes revealed that m<superscript>6</superscript>A targets key genes of many important context-related biological processes including embryonic development, stem cell differentiation, transcription, translation, cell death, cell proliferation and cancer-related pathways. These results demonstrate the power of FunDMDeep-m<superscript>6</superscript>A for elucidating m<superscript>6</superscript>A regulatory functions and its roles in biological processes and diseases. Availability and implementation The R-package for DMDeep-m<superscript>6</superscript>A is freely available from https://github.com/NWPU-903PR/DMDeepm6A1.0. Supplementary information Supplementary data are available at Bioinformatics online. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13674803
Volume :
35
Issue :
14
Database :
Complementary Index
Journal :
Bioinformatics
Publication Type :
Academic Journal
Accession number :
137399912
Full Text :
https://doi.org/10.1093/bioinformatics/btz316