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利用高密度 600K SNP 芯片对鸡喙畸形进行基于单 SNP 和通路的全基因组关联研究。

Single SNP- and pathway-based genome-wide association studies for beak deformity in chickens using high-density 600K SNP arrays.

机构信息

Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.

CapitalBio Corporation, Beijing, 102206, China.

出版信息

BMC Genomics. 2018 Jun 28;19(1):501. doi: 10.1186/s12864-018-4882-8.

Abstract

BACKGROUND

Beak deformity, typically expressed as the crossing of upper and lower mandibles, is found in several indigenous chicken breeds, including the Beijing-You chickens studied here. Beak deformity severely impairs the birds' growth and welfare. Although previous studies shed some light on the genetic regulation of this complex trait, the genetic basis of this malformation remains incompletely understood.

RESULTS

In this study, single SNP- and pathway-based genome-wide association studies (GWASs) were performed using ROADTRIPS and SNP ratio test (SRT), respectively. A total of 48 birds with deformed beaks (case) and 48 normal birds (control) were genotyped using Affymetrix 600 K HD genotyping arrays. As a result, 95 individuals and 429,539 SNPs were obtained after quality control. The P-value was corrected by a Bonferroni adjustment based on linkage disequilibrium pruning. The single SNP-based association study identified one associated SNP with 5% genome-wide significance and seven suggestively associated SNPs. Four high-confidence genes, LOC421892, TDRD3, RET, and STMN1, were identified as the most promising candidate genes underlying this complex trait in view of their positions, functions, and overlaps with previous studies. The pathway-based association study highlighted the association of six pathways with beak deformity, including the calcium signaling pathway.

CONCLUSIONS

Potentially useful candidate genes and pathways for beak deformity were identified, which should be the subject of further functional characterization.

摘要

背景

喙畸形,表现为上下颌交叉,在包括北京油鸡在内的几个本土鸡品种中都有发现。喙畸形严重损害了鸟类的生长和福利。尽管先前的研究揭示了这种复杂特征的遗传调控机制,但这种畸形的遗传基础仍不完全清楚。

结果

本研究分别采用 ROADTRIPS 和 SNP 比值检验(SRT)进行了单 SNP 和途径全基因组关联研究(GWAS)。使用 Affymetrix 600K HD 基因分型阵列对 48 只有畸形喙的鸟类(病例)和 48 只有正常喙的鸟类(对照)进行了基因分型。经过质量控制后,获得了 95 只个体和 429539 个 SNP。基于连锁不平衡修剪,用 Bonferroni 调整对 P 值进行了校正。基于单 SNP 的关联研究鉴定出一个与 5%全基因组显著相关的关联 SNP 和七个提示相关的 SNP。考虑到它们的位置、功能以及与先前研究的重叠,LOC421892、TDRD3、RET 和 STMN1 这四个高可信度基因被确定为该复杂性状的最有希望的候选基因。基于途径的关联研究强调了六个途径与喙畸形的关联,包括钙信号通路。

结论

鉴定出了与喙畸形相关的潜在有用候选基因和途径,这些基因和途径应该是进一步功能表征的主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3149/6022433/011cf72079b7/12864_2018_4882_Fig1_HTML.jpg

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