生物
收敛演化
休眠(计算)
染色质
遗传学
基因
基因组学
进化生物学
基因组
系统发育学
算法
计算机科学
国家(计算机科学)
作者
Elliott Ferris,Josue D. Gonzalez Murcia,Adriana Cristina Rodriguez,Susan Steinwand,Cornelia Stacher Hörndli,Dimitri Traenkner,Pablo J Maldonado-Catala,Christopher Gregg
标识
DOI:10.1101/2024.06.26.600891
摘要
Abstract Elucidating the genetic basis of mammalian metabolism could help define mechanisms central to health and disease. Here, we define conserved cis- regulatory elements (CREs) and programs for mammalian metabolic control. We delineate gene expression and chromatin responses in the mouse hypothalamus for 7 steps of the Fed-to-Fasted-to-Refed (FFR) response process. Comparative genomics of hibernating versus non-hibernating lineages then illuminates cis- elements showing convergent changes in hibernators. Hibernators accumulated loss-of-function effects for specific CREs regulating hypothalamic FFR responses. Multi-omics approaches pinpoint key CREs, genes, regulatory programs, and cell types in the divergence of hibernating and homeothermic lineages. The refeeding period after extended fasting is revealed as one critical period of chromatin remodeling with convergent genomic changes. This genetic framework is a step toward harnessing hibernator adaptations in medicine. One sentence summary Convergent signals define cis- regulatory mechanisms behind food scarcity responses and hibernator-homeotherm divergence.
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