Dr.Nod: computational framework for discovery of regulatory non-coding drivers in tissue-matched distal regulatory elements

Author:

Tomkova Marketa123ORCID,Tomek Jakub4ORCID,Chow Julie1ORCID,McPherson John D1,Segal David J135ORCID,Hormozdiari Fereydoun135ORCID

Affiliation:

1. Department of Biochemistry and Molecular Medicine, University of California , Davis, CA 95616, USA

2. Ludwig Cancer Research, University of Oxford , Oxford, OX3 7DQ, UK

3. UC Davis Genome Center, University of California , Davis, CA 95616, USA

4. Department of Pharmacology, University of California , Davis, CA 95616, USA

5. UC Davis MIND Institute, University of California , Davis, CA 95616, USA

Abstract

AbstractThe discovery of cancer driver mutations is a fundamental goal in cancer research. While many cancer driver mutations have been discovered in the protein-coding genome, research into potential cancer drivers in the non-coding regions showed limited success so far. Here, we present a novel comprehensive framework Dr.Nod for detection of non-coding cis-regulatory candidate driver mutations that are associated with dysregulated gene expression using tissue-matched enhancer-gene annotations. Applying the framework to data from over 1500 tumours across eight tissues revealed a 4.4-fold enrichment of candidate driver mutations in regulatory regions of known cancer driver genes. An overarching conclusion that emerges is that the non-coding driver mutations contribute to cancer by significantly altering transcription factor binding sites, leading to upregulation of tissue-matched oncogenes and down-regulation of tumour-suppressor genes. Interestingly, more than half of the detected cancer-promoting non-coding regulatory driver mutations are over 20 kb distant from the cancer-associated genes they regulate. Our results show the importance of tissue-matched enhancer-gene maps, functional impact of mutations, and complex background mutagenesis model for the prediction of non-coding regulatory drivers. In conclusion, our study demonstrates that non-coding mutations in enhancers play a previously underappreciated role in cancer and dysregulation of clinically relevant target genes.

Funder

NSF

UC-Davis start-up funds

Sloan Research Fellowship

Publisher

Oxford University Press (OUP)

Subject

Genetics

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Prediction of Non-coding Driver Mutations Using Ensemble Learning;2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM);2023-12-05

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