Pértille Fábio, Brantsæter Margrethe, Nordgreen Janicke, Coutinho Luiz Lehmann, Janczak Andrew M, Jensen Per, Guerrero-Bosagna Carlos
Avian Behavioral Genomics and Physiology Group, IFM Biology, Linköping University, SE-58 183 Linköping, Sweden.
Animal Biotechnology Laboratory, Animal Science and Pastures Department, University of São Paulo (USP)/ Luiz de Queiroz College of Agriculture (ESALQ), 13418-900 Piracicaba, São Paulo, Brazil.
J Exp Biol. 2017 Oct 1;220(Pt 19):3579-3587. doi: 10.1242/jeb.157891. Epub 2017 Aug 7.
Stressful conditions are common in the environment where production animals are reared. Stress in animals is usually determined by the levels of stress-related hormones. A big challenge, however, is in determining the history of exposure of an organism to stress, because the release of stress hormones can show an acute (and recent) but not a sustained exposure to stress. Epigenetic tools provide an alternative option to evaluate past exposure to long-term stress. Chickens provide a unique model to study stress effects in the epigenome of red blood cells (RBCs), a cell type of easy access and nucleated in birds. The present study investigated whether two different rearing conditions in chickens can be identified by looking at DNA methylation patterns in their RBCs later in life. These conditions were rearing in open aviaries versus in cages, which are likely to differ regarding the amount of stress they generate. Our comparison revealed 115 genomic windows with significant changes in RBC DNA methylation between experimental groups, which were located around 53 genes and within 22 intronic regions. Our results set the ground for future detection of long-term stress in live production animals by measuring DNA methylation in a cell type of easy accessibility.
在养殖生产动物的环境中,应激条件很常见。动物的应激通常由应激相关激素的水平决定。然而,一个巨大的挑战在于确定生物体过去的应激暴露史,因为应激激素的释放只能显示急性(近期)而非长期的应激暴露。表观遗传工具为评估过去长期应激暴露提供了另一种选择。鸡提供了一个独特的模型,用于研究应激对红细胞(RBC)表观基因组的影响,红细胞是鸟类中一种易于获取且有核的细胞类型。本研究调查了是否可以通过观察鸡在生命后期红细胞中的DNA甲基化模式来识别两种不同的饲养条件。这两种条件分别是在开放式鸟舍饲养和在笼子里饲养,它们产生的应激量可能不同。我们的比较揭示了115个基因组窗口,实验组之间红细胞DNA甲基化有显著变化,这些窗口位于约53个基因周围和22个内含子区域内。我们的结果为未来通过测量一种易于获取的细胞类型中的DNA甲基化来检测活体生产动物的长期应激奠定了基础。