| Literature DB >> 25480298 |
Anita Öst1, Adelheid Lempradl2, Eduard Casas3, Melanie Weigert2, Theodor Tiko2, Merdin Deniz2, Lorena Pantano4, Ulrike Boenisch2, Pavel M Itskov5, Marlon Stoeckius6, Marius Ruf2, Nikolaus Rajewsky6, Gunter Reuter7, Nicola Iovino2, Carlos Ribeiro5, Mattias Alenius8, Steffen Heyne2, Tanya Vavouri3, J Andrew Pospisilik9.
Abstract
The global rise in obesity has revitalized a search for genetic and epigenetic factors underlying the disease. We present a Drosophila model of paternal-diet-induced intergenerational metabolic reprogramming (IGMR) and identify genes required for its encoding in offspring. Intriguingly, we find that as little as 2 days of dietary intervention in fathers elicits obesity in offspring. Paternal sugar acts as a physiological suppressor of variegation, desilencing chromatin-state-defined domains in both mature sperm and in offspring embryos. We identify requirements for H3K9/K27me3-dependent reprogramming of metabolic genes in two distinct germline and zygotic windows. Critically, we find evidence that a similar system may regulate obesity susceptibility and phenotype variation in mice and humans. The findings provide insight into the mechanisms underlying intergenerational metabolic reprogramming and carry profound implications for our understanding of phenotypic variation and evolution.Entities:
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Year: 2014 PMID: 25480298 DOI: 10.1016/j.cell.2014.11.005
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582