Chromatin accessibility dynamics reveal novel functional enhancers in C. elegans

• Published in: Genome research 2017-12, Vol.27 (12), p.2096-2107
• Main Authors: Daugherty, Aaron C, Yeo, Robin W, Buenrostro, Jason D, Greenleaf, William J, Kundaje, Anshul, Brunet, Anne
• Format: Article
• Language: English
• Subjects: Amino Acid Motifs; Animals; Caenorhabditis elegans - genetics; Caenorhabditis elegans - growth & development; Caenorhabditis elegans Proteins - metabolism; Chromatin - chemistry; Chromatin - metabolism; Chromatin Assembly and Disassembly; DNA, Helminth; Enhancer Elements, Genetic; Epigenesis, Genetic; Nuclear Proteins - metabolism; Resource
• ISSN: 1088-9051; 1549-5469
• DOI: 10.1101/gr.226233.117

Chromatin accessibility, a crucial component of genome regulation, has primarily been studied in homogeneous and simple systems, such as isolated cell populations or early-development models. Whether chromatin accessibility can be assessed in complex, dynamic systems in vivo with high sensitivity remains largely unexplored. In this study, we use ATAC-seq to identify chromatin accessibility changes in a whole animal, the model organism , from embryogenesis to adulthood. Chromatin accessibility changes between developmental stages are highly reproducible, recapitulate histone modification changes, and reveal key regulatory aspects of the epigenomic landscape throughout organismal development. We find that over 5000 distal noncoding regions exhibit dynamic changes in chromatin accessibility between developmental stages and could thereby represent putative enhancers. When tested in vivo, several of these putative enhancers indeed drive novel cell-type- and temporal-specific patterns of expression. Finally, by integrating transcription factor binding motifs in a machine learning framework, we identify EOR-1 as a unique transcription factor that may regulate chromatin dynamics during development. Our study provides a unique resource for , a system in which the prevalence and importance of enhancers remains poorly characterized, and demonstrates the power of using whole organism chromatin accessibility to identify novel regulatory regions in complex systems.