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首页> 外文期刊>BMC Genomics >Genome-wide identification of copy number variations between two chicken lines that differ in genetic resistance to Marek’s disease
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Genome-wide identification of copy number variations between two chicken lines that differ in genetic resistance to Marek’s disease

机译:全基因组范围内鉴定两条对马立克氏病具有不同遗传抗性的鸡系之间的拷贝数变异

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摘要

Background Copy number variation (CNV) is a major source of genome polymorphism that directly contributes to phenotypic variation such as resistance to infectious diseases. Lines 6 3 and 7 2 are two highly inbred experimental chicken lines that differ greatly in susceptibility to Marek’s disease (MD), and have been used extensively in efforts to identify the genetic and molecular basis for genetic resistance to MD. Using next generation sequencing, we present a genome-wide assessment of CNVs that are potentially associated with genetic resistance to MD. Methods Three chickens randomly selected from each line were sequenced to an average depth of 20×. Two popular software, CNVnator and Pindel, were used to call genomic CNVs separately. The results were combined to obtain a union set of genomic CNVs in the two chicken lines. Results A total of 5,680 CNV regions (CNVRs) were identified?after merging the two datasets, of which 1,546 and 1,866 were specific to the MD resistant or susceptible line, respectively. Over half of the line-specific CNVRs were shared by 2 or more chickens, reflecting the reduced diversity in both inbred lines. The CNVRs fixed in the susceptible lines were significantly enriched in genes involved in MAPK signaling pathway. We also found 67 CNVRs overlapping with 62 genes previously shown to be strong candidates of the underlying genes responsible for the susceptibility to MD. Conclusions Our findings provide new insights into the genetic architecture of the two chicken lines and additional evidence that MAPK signaling pathway may play an important role in host response to MD virus infection. The rich source of line-specific CNVs is valuable for future disease-related association studies in the two chicken lines.
机译:背景拷贝数变异(CNV)是基因组多态性的主要来源,其直接导致了表型变异,例如对传染病的抵抗力。品系6 3 和7 2 是两个高度近交的实验鸡品系,它们对马立克氏病(MD)的敏感性差异很大,并已广泛用于鉴定遗传和遗传基础对MD的抗药性。使用下一代测序,我们提出了CNV的全基因组评估,其可能与MD的遗传抗性相关。方法从各系中随机选择三只鸡,测序平均深度为20倍。使用两个流行的软件CNVnator和Pindel分别调用基因组CNV。合并结果以在两条鸡系中获得基因组CNV的并集。结果合并两个数据集后,共鉴定出5680个CNV区域(CNVR),其中1546个和1866个对MD抗性或易感品系具有特异性。超过一半的品系特异性CNVR被2只或更多只鸡共享,这反映了两种自交系的多样性降低。固定在易感株系中的CNVRs显着富集了与MAPK信号通路有关的基因。我们还发现67个CNVR与62个基因重叠,这些基因先前被证明是引起MD易感性的潜在基因的强大候选者。结论我们的发现为两条鸡系的遗传结构提供了新见解,并提供了另外的证据表明MAPK信号通路可能在宿主对MD病毒感染的应答中起重要作用。品系特异性CNV的丰富来源对于两条鸡品系未来与疾病相关的关联研究具有重要价值。

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