Key Laboratory of Animal Genetics Breeding and Reproduction (Poultry), Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Chifeng Agriculture and Animal Husbandry Science Academy, Chifeng 024031, Inner Mongolia, China.
Poult Sci. 2019 Apr 1;98(4):1833-1841. doi: 10.3382/ps/pey519.
The beak is the dominant avian facial feature, and beak deformity occurs in 0.5 to 2.5% of some indigenous chicken breeds, resulting in difficulties when eating, drinking, and performing natural behaviors. Previous studies on beak deformity focused largely on candidate molecules associated with skeletogenic development, providing insight into the molecular and genetic underpinnings of beak deformity. The present study was performed to identify candidate proteins related to this malformation in chickens. Three 12-day-old Beijing-You roosters with deformed beaks (D1, D2, and D3) and 3 with normal beaks (N1, N2, and N3) were used, and total beak proteins were isolated and subjected to standard iTRAQ labeling, strong cation-exchange chromatography, and liquid chromatography-tandem mass spectrometry. Mascot 2.3.02 was used to identify and quantitatively analyze proteins. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were used to identify functions and metabolic pathways of differentially expressed proteins, and key proteins were further validated using western blot. A total of 2,370, 2,401, and 2,378 proteins were reliably quantified in 3 biological replicates, among which, 2,345 were common to all, and 92 were differentially expressed between the 2 groups. These included 37 upregulated and 55 downregulated proteins in deformed beaks. Pentraxin-related protein 3, hemopexin, lipoprotein lipase, retinoid-binding protein 7, and biliverdin reductase A were downregulated in all 3 sets, while parvalbumin, peptidyl-prolyl cis-trans isomerase, and ubiquitin-fold modifier 1 were upregulated. Pathway analysis returned no enriched pathways, and western blot validated the iTRAQ results. Parvalbumin and lipoprotein lipase could be firstly selected as key proteins in view of their known functions in regulating the buffering of intracellular free Ca2+ in both cartilage and bone cells and bone mass, respectively. Their potential roles in beak deformity, however, deserve further studies. In summary, the onset of beak deformity could be very complex, and this study will be helpful for future investigation of mechanistic explanation for beak deformity.
喙是鸟类的主要面部特征,0.5%至 2.5%的某些本地鸡品种存在喙畸形,导致进食、饮水和进行自然行为困难。先前关于喙畸形的研究主要集中在与骨骼发育相关的候选分子上,为喙畸形的分子和遗传基础提供了深入了解。本研究旨在鉴定与鸡畸形相关的候选蛋白质。使用了 3 只 12 日龄具有畸形喙的北京油鸡(D1、D2 和 D3)和 3 只具有正常喙的北京油鸡(N1、N2 和 N3),分离总喙蛋白并进行标准 iTRAQ 标记、强阳离子交换色谱和液相色谱-串联质谱分析。Mascot 2.3.02 用于鉴定和定量分析蛋白质。GO 和京都基因与基因组百科全书通路富集分析用于鉴定差异表达蛋白的功能和代谢途径,并用 Western blot 进一步验证关键蛋白。在 3 个生物学重复中,共可靠定量了 2370、2401 和 2378 种蛋白质,其中 2345 种在所有组中共同存在,92 种在 2 组之间差异表达。这些蛋白包括 37 种上调和 55 种下调的畸形喙中的蛋白。Pentraxin 相关蛋白 3、血红素结合蛋白、脂蛋白脂肪酶、视黄醇结合蛋白 7 和胆红素还原酶 A 在所有 3 组中均下调,而副甲状腺蛋白、肽基脯氨酰顺反异构酶和泛素折叠修饰酶 1 上调。通路分析没有返回富集通路,Western blot 验证了 iTRAQ 结果。考虑到副甲状腺蛋白和脂蛋白脂肪酶在调节软骨和骨细胞以及骨量中细胞内游离 Ca2+的缓冲方面的已知功能,它们可以首先被选为关键蛋白。然而,它们在喙畸形中的潜在作用值得进一步研究。总之,喙畸形的发病机制可能非常复杂,本研究将有助于进一步研究喙畸形的机制解释。