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鸡外周血嗜酸性粒细胞/淋巴细胞(H/L)比值的全基因组关联研究和通路分析。

Genome-Wide Association Study and Pathway Analysis for Heterophil/Lymphocyte (H/L) Ratio in Chicken.

机构信息

State Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.

出版信息

Genes (Basel). 2020 Aug 27;11(9):1005. doi: 10.3390/genes11091005.

Abstract

Disease control and prevention have been critical factors in the dramatic growth of the poultry industry. Disease resistance in chickens can be improved through genetic selection for immunocompetence. The heterophil/lymphocyte ratio (H/L) in the blood reflects the immune system status of chickens. Our objective was to conduct a genome-wide association study (GWAS) and pathway analysis to identify possible biological mechanisms involved in H/L traits. In this study, GWAS for H/L was performed in 1317 Cobb broilers to identify significant single-nucleotide polymorphisms (SNPs) associated with H/L. Eight SNPs ( < 1/8068) reached a significant level of association. The significant SNP on GGA 19 (chicken chromosome 19) was in the gene for complement C1q binding protein (). The wild-type and mutant individuals showed significant differences in H/L at five identified SNPs ( < 0.05). According to the results of pathway analysis, nine associated pathways ( < 0.05) were identified. By combining GWAS with pathway analysis, we found that all SNPs after QC explained 12.4% of the phenotypic variation in H/L, and 52 SNPs associated with H/L explained as much as 9.7% of the phenotypic variation in H/L. Our findings contribute to understanding of the genetic regulation of H/L and provide theoretical support.

摘要

疾病控制和预防一直是家禽养殖业快速发展的关键因素。通过对免疫能力进行遗传选择,可以提高鸡的抗病能力。血液中的异嗜性/淋巴细胞比值(H/L)反映了鸡的免疫系统状态。我们的目的是进行全基因组关联研究(GWAS)和通路分析,以确定与 H/L 特征相关的可能生物学机制。本研究对 1317 只科宝肉鸡进行了 H/L 的全基因组关联分析,以鉴定与 H/L 相关的显著单核苷酸多态性(SNP)。有 8 个 SNP(<1/8068)达到了显著关联水平。在鸡 19 号染色体(GGA 19)上的显著 SNP 位于补体 C1q 结合蛋白()基因中。在五个已鉴定的 SNP 中(<0.05),野生型和突变个体的 H/L 存在显著差异。根据通路分析的结果,鉴定到了 9 个相关通路(<0.05)。通过将 GWAS 与通路分析相结合,我们发现经过 QC 后的所有 SNP 可以解释 H/L 表型变异的 12.4%,而与 H/L 相关的 52 个 SNP 则可以解释高达 9.7%的 H/L 表型变异。我们的研究结果有助于理解 H/L 的遗传调控,并提供了理论支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d70/7563235/358ab4cb079b/genes-11-01005-g001.jpg

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