Bai H, Sun Y, Liu N, Liu Y, Xue F, Li Y, Xu S, Ni A, Ye J, Chen Y, Chen J
Key Laboratory of Animal Genetics Breeding and Reproduction (Poultry), Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Beijing General Station of Animal Husbandry Service, Beijing, 102200, China.
Anim Genet. 2018 Jun;49(3):226-236. doi: 10.1111/age.12652. Epub 2018 Apr 11.
Beak deformity (crossed beaks) is found in several indigenous chicken breeds including Beijing-You studied here. Birds with deformed beaks have reduced feed intake and poor production performance. Recently, copy number variation (CNV) has been examined in many species and is recognized as a source of genetic variation, especially for disease phenotypes. In this study, to unravel the genetic mechanisms underlying beak deformity, we performed genome-wide CNV detection using Affymetrix chicken high-density 600K data on 48 deformed-beak and 48 normal birds using penncnv. As a result, two and eight CNV regions (CNVRs) covering 0.32 and 2.45 Mb respectively on autosomes were identified in deformed-beak and normal birds respectively. Further RT-qPCR studies validated nine of the 10 CNVRs. The ratios of six CNVRs were significantly different between deformed-beak and normal birds (P < 0.01). Within these six regions, three and 21 known genes were identified in deformed-beak and normal birds respectively. Bioinformatics analysis showed that these genes were enriched in six GO terms and one KEGG pathway. Five candidate genes in the CNVRs were further validated using RT-qPCR. The expression of LRIG2 (leucine rich repeats and immunoglobulin like domains 2) was lower in birds with deformed beaks (P < 0.01). Therefore, the LRIG2 gene could be considered a key factor in view of its known functions and its potential roles in beak deformity. Overall, our results will be helpful for future investigations of the genomic structural variations underlying beak deformity in chickens.
喙畸形(交叉喙)在包括本研究中的北京油鸡在内的多个本土鸡品种中都有发现。喙畸形的鸡采食量减少,生产性能较差。近年来,拷贝数变异(CNV)已在许多物种中得到研究,并被认为是遗传变异的一个来源,尤其是对于疾病表型而言。在本研究中,为了揭示喙畸形背后的遗传机制,我们使用Affymetrix鸡高密度600K数据,通过penncnv软件对48只喙畸形鸡和48只正常鸡进行了全基因组CNV检测。结果分别在喙畸形鸡和正常鸡的常染色体上鉴定出两个和八个CNV区域(CNVRs),分别覆盖0.32 Mb和2.45 Mb。进一步的RT-qPCR研究验证了10个CNVRs中的9个。喙畸形鸡和正常鸡之间6个CNVRs的比例存在显著差异(P < 0.01)。在这6个区域内,喙畸形鸡和正常鸡分别鉴定出3个和21个已知基因。生物信息学分析表明,这些基因在6个基因本体(GO)术语和1条京都基因与基因组百科全书(KEGG)通路中富集。对CNVRs中的5个候选基因进一步进行了RT-qPCR验证。富含亮氨酸重复序列和免疫球蛋白样结构域2(LRIG2)基因在喙畸形鸡中的表达较低(P < 0.01)。因此,鉴于LRIG2基因的已知功能及其在喙畸形中的潜在作用,它可被视为一个关键因素。总体而言,我们的研究结果将有助于未来对鸡喙畸形潜在基因组结构变异的研究。