Steinerova Michala, Horecky Cenek, Horecka Eliska, Knoll Ales, Nedomova Sarka, Slama Petr, Pavlik Ales
Department of Animal Morphology, Physiology and Genetics, Mendel University in Brno, Faculty of AgriSciences, Zemědělská 1/1665, 613 00 Brno, Czech Republic.
Department of Food Technology, Mendel University in Brno, Faculty of AgriSciences, Zemědělská 1/1665, 613 00 Brno, Czech Republic.
Saudi J Biol Sci. 2022 Apr;29(4):2526-2531. doi: 10.1016/j.sjbs.2021.12.024. Epub 2021 Dec 16.
The Wnt signaling pathway plays a critical role in almost all aspects of skeletal development and homeostasis. Many studies suggest the importance of this signaling pathway in connection with bone metabolism through many skeletal disorders caused by mutations in Wnt signaling genes. The knowledge gained through targeting this pathway is of great value for skeletal health and diseases, for example of increased bone mass in the case of osteoporosis. Our objective was to focus on the detection of single nucleotide polymorphisms and investigate the associations between possible polymorphisms in selected genes that are part of those signaling pathways and parameters of bones in hens of ISA Brown hybrids (bone breaking strength, length, width, and bone mass). Different regions of the and genes were studied, using PCR and sequencing, in a total of forty-eight samples for each marker. Thirteen polymorphisms have been discovered in selected regions of studied genes, whereas these polymorphisms were only within the gene. Eight of these polymorphisms were synonymous and five were in the intron. The tested regions of the and genes were monomorphic. The only statistically significant difference was found within the gene (exon 2) and the bone length parameter, in the c.443 + 86G > A polymorphism. However, this polymorphism was found in the intron, and no other one was found within the selected regions to show associations with the observed bone parameters.
Wnt信号通路在骨骼发育和稳态的几乎所有方面都起着关键作用。许多研究表明,通过Wnt信号基因的突变引起的许多骨骼疾病,该信号通路在骨代谢方面具有重要意义。通过针对该通路所获得的知识对于骨骼健康和疾病具有重要价值,例如在骨质疏松症的情况下增加骨量。我们的目标是专注于单核苷酸多态性的检测,并研究作为这些信号通路一部分的选定基因中可能的多态性与ISA Brown杂交母鸡骨骼参数(骨断裂强度、长度、宽度和骨量)之间的关联。使用PCR和测序技术,对每个标记总共48个样本的 和 基因的不同区域进行了研究。在所研究基因的选定区域中发现了13个多态性,而这些多态性仅存在于 基因内。其中8个多态性是同义的,5个在内含子中。 和 基因的测试区域是单态的。在 基因(外显子2)和骨长度参数中,在c.443 + 86G > A多态性中发现了唯一具有统计学意义的差异。然而,这种多态性存在于内含子中,并且在选定区域内未发现其他与观察到的骨骼参数相关的多态性。