Bai Hao, Sun Yanyan, Zhu Jing, Liu Nian, Li Dongli, Xue Fuguang, Li Yunlei, Chen Jilan
Key Laboratory of Genetics Resources and Utilization of Livestock, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
BMC Genet. 2016 Feb 18;17:44. doi: 10.1186/s12863-016-0353-x.
The beak deformity (crossed beaks) was found in some indigenous chickens of China, such as Beijing-You (BJY), Qingyuan Partridge, and Huxu Chickens. Birds with deformed beaks have reduced feed intake and drinking, impeded growth rate, and poor production performance. Beak deformity reduces the economy of poultry industry and affects animal welfare as well. The genetic basis of this malformation remains incompletely understood. LOC426217, also named claw keratin-like, was the most up-regulated gene in the deformed beaks from a previous digital gene expression (DGE) analysis and was selected as an important candidate gene for further analysis.
In the present study, quantitative real-time PCR (qRT-PCR) was firstly performed to determine the expression pattern of LOC426217 gene in deformed and normal beaks to verify the DGE results. Tissue-specific expression profile of this gene in 14 tissues was also determined using qRT-PCR. The LOC426217 was amplified from the genomic DNA of 171 deformed and 164 normal beaks, and sequenced to detect the single nucleotide polymorphisms (SNPs). The results showed that LOC426217 was significantly high-expressed in the deformed beaks, which was in good agreement with the DGE results. This gene was specifically high-expressed in beaks than other tissues. Eight SNPs were detected in LOC426217: -62G > T, 24 T > C, 36G > C, 192A > T, 204C > T, 222 T > C, 285G > T, and 363 T > C. Genotype frequency of G-62 T, T24C, G36C, T222C, and T363C loci was significant different between deformed and normal beaks. Haplotype analysis revealed one block with SNPs T24C and G36C, and one block with SNPs A192T, C204T, T222C, and G285T in normal birds, while the block with SNPs G36C and A192T in deformed ones.
It was concluded from these results that the over-expression of LOC426217 in the beak maybe related to the malformation. The polymorphisms of LOC426217 gene were associated with the beak deformity trait where the SNPs of G-62 T, T24C, G36C, T222C, and T363C loci maybe used as markers. The specific haplotype block in deformed birds may be a potential linkage marker for this trait.
在中国的一些地方鸡种中发现了喙畸形(交叉喙),如北京油鸡(BJY)、清远麻鸡和胡须鸡。喙畸形的鸡采食量和饮水量减少,生长速度受阻,生产性能较差。喙畸形降低了家禽业的经济效益,也影响了动物福利。这种畸形的遗传基础仍未完全了解。LOC426217,也称为爪角蛋白样蛋白,是先前数字基因表达(DGE)分析中畸形喙中上调最明显的基因,并被选为进一步分析的重要候选基因。
在本研究中,首先进行了定量实时PCR(qRT-PCR)以确定LOC426217基因在畸形喙和正常喙中的表达模式,以验证DGE结果。还使用qRT-PCR确定了该基因在14种组织中的组织特异性表达谱。从171只畸形喙和164只正常喙的基因组DNA中扩增出LOC426217,并进行测序以检测单核苷酸多态性(SNP)。结果表明,LOC426217在畸形喙中显著高表达,这与DGE结果高度一致。该基因在喙中的表达明显高于其他组织。在LOC426217中检测到8个SNP:-62G>T、24T>C、36G>C、192A>T、204C>T、222T>C、285G>T和363T>C。G-62T、T24C、G36C、T222C和T363C位点的基因型频率在畸形喙和正常喙之间存在显著差异。单倍型分析显示,正常鸡中有一个包含SNP T24C和G36C的单倍型块,以及一个包含SNP A192T、C204T、T222C和G285T的单倍型块,而畸形鸡中有一个包含SNP G36C和A192T的单倍型块。
从这些结果可以得出结论,LOC426217在喙中的过度表达可能与畸形有关。LOC426217基因的多态性与喙畸形性状相关,其中G-62T、T24C、G36C、T222C和T363C位点的SNP可作为标记。畸形鸡中特定的单倍型块可能是该性状的潜在连锁标记。