鸡啄羽行为的人工选择分化对遗传和神经表观遗传的影响

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2024-12-19 DOI:10.1186/s12864-024-11137-w
Elske N de Haas, Fábio Pértille, Joergen B Kjaer, Per Jensen, Carlos Guerrero-Bosagna
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引用次数: 0

摘要

啄羽毛(FP)是鸡的一种重复行为,受遗传、表观遗传和环境因素的影响,类似于人类发育障碍(如多动症、自闭症)的行为。本研究考察了从高或低FP行为(HFP或LFP)中选择的七代鸡的丘脑中的遗传和神经表观遗传因素。在这个受控的人工选择过程中,我们整合了差异甲基化区域(DMRs)、单核苷酸多态性(SNPs)和拷贝数变异(CNVs)的数据。在行为、免疫学和神经学方面的显著差异已被报道。我们在这些品系中发现了710个snp,这些snp表明了新的潜在重要FP基因,如TMPRSS6(与自闭症有关),SST和ARNT2(生长抑素功能)。遗传变异在选择过程中受基因组水平的影响最大。最大的CNVs分别出现在RIC3 (HFP增加)和SH3RF2 (LFP增加)基因上,这两个基因分别与烟碱乙酰胆碱受体调节和人类肿瘤发生有关。我们的研究还表明启动子和内含子是CpG耗竭的热点。本研究利用公共FP定量性状位点(QTL)数据库的数据研究了组学水平的重叠,揭示了理解重复行为的新候选基因,如RTKN2,与人类阿尔茨海默病相关。这项研究表明,CNVs是基因组多样化的关键初始步骤,可能比snp更有影响力。
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Genetic and neuro-epigenetic effects of divergent artificial selection for feather pecking behaviour in chickens.

Feather pecking (FP) is a repetitive behaviour in chickens, influenced by genetic, epigenetic, and environmental factors, similar to behaviours seen in human developmental disorders (e.g., hyperactivity, autism). This study examines genetic and neuro-epigenetic factors in the thalamus of chickens from lines selected for seven generations for high or low FP behaviour (HFP or LFP). We integrate data on Differentially Methylated Regions (DMRs), Single Nucleotide Polymorphisms (SNPs), and Copy Number Variations (CNVs) in this controlled artificial selection process. Significant differences in behaviour, immunology, and neurology have been reported in these lines. We identified 710 SNPs in these lines that indicate new potentially important genes for FP such as TMPRSS6 (implicated in autism), and SST and ARNT2 (somatostatin function). CNV were the omic level most affected during selection. The largest CNVs found were in RIC3 (gain in HFP) and SH3RF2 (gain in LFP) genes, linked to nicotinic acetylcholine receptor regulation and human oncogenesis, respectively. Our study also suggests that promoters and introns are hotspots for CpG depletion. The overlapping of the omic levels investigated here with data from a public FP Quantitative Trait Loci (QTL) database revealed novel candidate genes for understanding repetitive behaviours, such as RTKN2, associated with Alzheimer's disease in humans. This study suggests CNVs as a crucial initial step for genomic diversification, potentially more impactful than SNPs.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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