Paternal Diet Defines Offspring Chromatin State and Intergenerational Obesity

被引:285
|
作者
Ost, Anita [1 ,6 ]
Lempradl, Adelheid [1 ]
Casas, Eduard [2 ,3 ]
Weigert, Melanie [1 ]
Tiko, Theodor [1 ]
Deniz, Merdin [1 ]
Pantano, Lorena [2 ]
Boenisch, Ulrike [1 ]
Itskov, Pavel M. [7 ]
Stoeckius, Marlon [4 ]
Ruf, Marius [1 ]
Rajewsky, Nikolaus [4 ]
Reuter, Gunter [5 ]
Iovino, Nicola [1 ]
Ribeiro, Carlos [7 ]
Alenius, Mattias [6 ]
Heyne, Steffen [1 ]
Vavouri, Tanya [2 ,3 ]
Pospisilik, J. Andrew [1 ]
机构
[1] Max Planck Inst Immunobiol & Epigenet, D-79108 Freiburg, Germany
[2] Inst Med Predict & Personalitzada Canc, Barcelona 08916, Spain
[3] ICO Hosp GermansTrias & Pujol, Josep Carreras Leukaemia Res Inst IJC, Barcelona 08916, Spain
[4] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[5] Univ Halle Wittenberg, Inst Biol, D-06120 Halle, Germany
[6] Linkoping Univ, Dept Clin & Expt Med, S-58183 Linkoping, Sweden
[7] Champalimaud Ctr Unknown, Champalimaud Neurosci Programme, P-1400038 Lisbon, Portugal
基金
欧洲研究理事会;
关键词
TRANSGENERATIONAL EPIGENETIC INHERITANCE; HIGH-FAT DIET; GENE-EXPRESSION; DROSOPHILA-MELANOGASTER; C; ELEGANS; MICE; GENOME; TRANSMISSION; ADIPOCYTES; GERMLINE;
D O I
10.1016/j.cell.2014.11.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1352 / 1364
页数:13
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