利用估算的序列水平基因型,对因啄羽而被分化选择的蛋鸡品系进行全基因组关联研究的元分析。

IF 2.9 Q2 Biochemistry, Genetics and Molecular Biology
Clemens Falker-Gieske, Hanna Iffland, Siegfried Preuß, Werner Bessei, Cord Drögemüller, Jörn Bennewitz, Jens Tetens
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引用次数: 0

摘要

背景:啄羽(FP)是蛋鸡的一种破坏性行为,会给全球蛋鸡业造成经济损失,并严重损害动物福利。本研究的目的是发现导致啄羽行为的遗传变异和受影响基因。为此,我们通过对创始个体和半同父异母个体进行全基因组测序,从两个不同的蛋鸡群体中归纳出了低密度基因型,并将这些基因型进行了序列分析。为了破译FP的遗传结构,我们对两个资源种群进行了全基因组关联研究和荟萃分析,重点研究了 "啄羽次数"(FPD)和 "母鸡属于极端啄羽亚群的后验概率"(pEFP)这两个性状:在这项荟萃分析中,我们发现了许多受多态性影响的基因,这些基因与FPD性状显著相关。其中 SPATS2L、ZEB2、KCHN8 和 MRPL13 以前曾与精神疾病有关,后两者对尼古丁治疗有反应。基因组富集分析表明,磷脂酰肌醇信号转导受全球基因组分析中发现的基因的影响,高尔基体和大脑结构可能与 FP 表型的形成有关。此外,我们还验证了之前在 GGA1 上发现的 pEFP 性状 QTL,该 QTL 包含影响 NIPA1、KIAA1211L、AFF3 和 TSGA10 的变异:我们提供了许多基因参与FP行为倾向的证据,这些基因有助于针对这种不受欢迎的性状进行选择。此外,我们还发现了参与磷脂酰肌醇信号转导、高尔基体代谢和细胞结构的变异基因,因此我们认为大脑结构的变化是 FP 的一个影响因素,这在人类神经精神疾病中已有描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meta-analyses of genome wide association studies in lines of laying hens divergently selected for feather pecking using imputed sequence level genotypes.

Background: Feather pecking (FP) is damaging behavior in laying hens leading to global economic losses in the layer industry and massive impairments of animal welfare. The objective of the study was to discover genetic variants and affected genes that lead to FP behavior. To achieve that we imputed low-density genotypes from two different populations of layers divergently selected for FP to sequence level by performing whole genome sequencing on founder and half-sib individuals. In order to decipher the genetic structure of FP, genome wide association studies and meta-analyses of two resource populations were carried out by focusing on the traits 'feather pecks delivered' (FPD) and the 'posterior probability of a hen to belong to the extreme feather pecking subgroup' (pEFP).

Results: In this meta-analysis, we discovered numerous genes that are affected by polymorphisms significantly associated with the trait FPD. Among them SPATS2L, ZEB2, KCHN8, and MRPL13 which have been previously connected to psychiatric disorders with the latter two being responsive to nicotine treatment. Gene set enrichment analysis revealed that phosphatidylinositol signaling is affected by genes identified in the GWAS and that the Golgi apparatus as well as brain structure may be involved in the development of a FP phenotype. Further, we were able to validate a previously discovered QTL for the trait pEFP on GGA1, which contains variants affecting NIPA1, KIAA1211L, AFF3, and TSGA10.

Conclusions: We provide evidence for the involvement of numerous genes in the propensity to exhibit FP behavior that could aid in the selection against this unwanted trait. Furthermore, we identified variants that are involved in phosphatidylinositol signaling, Golgi metabolism and cell structure and therefore propose changes in brain structure to be an influential factor in FP, as already described in human neuropsychiatric disorders.

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来源期刊
BMC Genetics
BMC Genetics 生物-遗传学
CiteScore
4.30
自引率
0.00%
发文量
77
审稿时长
4-8 weeks
期刊介绍: BMC Genetics is an open access, peer-reviewed journal that considers articles on all aspects of inheritance and variation in individuals and among populations.
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