@article{dd12e88807c6465e956fe8d43a91ed30,
title = "Genome-wide analysis of cis-regulatory changes underlying metabolic adaptation of cavefish",
abstract = "Cis-regulatory changes are key drivers of adaptative evolution. However, their contribution to the metabolic adaptation of organisms is not well understood. Here, we used a unique vertebrate model, Astyanax mexicanus—different morphotypes of which survive in nutrient-rich surface and nutrient-deprived cave waters—to uncover gene regulatory networks underlying metabolic adaptation. We performed genome-wide epigenetic profiling in the liver tissues of Astyanax and found that many of the identified cis-regulatory elements (CREs) have genetically diverged and have differential chromatin features between surface and cave morphotypes, while retaining remarkably similar regulatory signatures between independently derived cave populations. One such CRE in the hpdb gene harbors a genomic deletion in cavefish that abolishes IRF2 repressor binding and derepresses enhancer activity in reporter assays. Selection of this mutation in multiple independent cave populations supports its importance in cave adaptation, and provides novel molecular insights into the evolutionary trade-off between loss of pigmentation and adaptation to food-deprived caves.",
author = "Jaya Krishnan and Seidel, {Chris W.} and Ning Zhang and Singh, {Narendra Pratap} and Jake VanCampen and Robert Peu{\ss} and Shaolei Xiong and Alexander Kenzior and Hua Li and Conaway, {Joan W.} and Nicolas Rohner",
note = "Funding Information: We are grateful to the cavefish and aquatics core facilities at the Stowers Institute for Medical Research for the support and husbandry of the cavefish and zebrafish. DNA samples for wild-caught Tinaja, Yerbaniz, Piedras and Japon{\'e}s cavefish were generously provided by R. Borowsky, and B. Jeffery provided Astyanax liver samples for preliminary ChIP experiments. We thank M. Cook for assistance with the motif analysis software, K. Weaver for assistance with high-throughput genotyping, and M. Miller for illustrations. We thank R. Krumlauf and J. Zeitlinger for useful input throughout the study and critical reading of the manuscript. N.R. is supported by institutional funding, National Institutes of Health (NIH) grants 1DP2AG071466-01 and R01 GM127872, and the National Science Foundation (NSF) EDGE award 1923372. R.P. was supported by a grant (no. PE 2807/1-1) from Deutsche Forschungsgemeinschaft. Publisher Copyright: {\textcopyright} 2022, The Author(s), under exclusive licence to Springer Nature America, Inc.",
year = "2022",
month = may,
doi = "10.1038/s41588-022-01049-4",
language = "English (US)",
volume = "54",
pages = "684--693",
journal = "Nature Genetics",
issn = "1061-4036",
publisher = "Nature Publishing Group",
number = "5",
}