Literature DB >> 32443951

Enhancer Predictions and Genome-Wide Regulatory Circuits.

Michael A Beer1, Dustin Shigaki1, Danwei Huangfu2.   

Abstract

Spatiotemporal control of gene expression during development requires orchestrated activities of numerous enhancers, which are cis-regulatory DNA sequences that, when bound by transcription factors, support selective activation or repression of associated genes. Proper activation of enhancers is critical during embryonic development, adult tissue homeostasis, and regeneration, and inappropriate enhancer activity is often associated with pathological conditions such as cancer. Multiple consortia [e.g., the Encyclopedia of DNA Elements (ENCODE) Consortium and National Institutes of Health Roadmap Epigenomics Mapping Consortium] and independent investigators have mapped putative regulatory regions in a large number of cell types and tissues, but the sequence determinants of cell-specific enhancers are not yet fully understood. Machine learning approaches trained on large sets of these regulatory regions can identify core transcription factor binding sites and generate quantitative predictions of enhancer activity and the impact of sequence variants on activity. Here, we review these computational methods in the context of enhancer prediction and gene regulatory network models specifying cell fate.

Entities:  

Keywords:  cell fate switching; enhancers; gene regulatory networks; machine learning; sequence-based prediction

Mesh:

Year:  2020        PMID: 32443951      PMCID: PMC7644210          DOI: 10.1146/annurev-genom-121719-010946

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  73 in total

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Journal:  Genome Res       Date:  2012-09       Impact factor: 9.043

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4.  A comprehensive integrated post-GWAS analysis of Type 1 diabetes reveals enhancer-based immune dysregulation.

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