Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China; Ministry of Agriculture, Forestry and Food Engineering, Yibin University, Yibin, 644000, China.
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Poult Sci. 2022 Apr;101(4):101697. doi: 10.1016/j.psj.2022.101697. Epub 2022 Jan 8.
Calcification of bones is the critical process of bone development in birds, which is very important for sustaining the normal biological function of bones. Light is one of the vital factors affecting bone development, but whether light intensity affects bone calcification and the underlying mechanism is still unknown. In this study, we used duck sternum as a model to analyze the calcification process under different light regimes. In addition, the underlying mechanism was also illustrated by integrating metabolomics and transcriptome methods. The experiment lasted from 14 to 51 d of duck age. The control group (LP1) kept light intensity 2 lx during the whole experiment. The two light supplement groups (LP2, LP3) were given light with the intensity of 70 lx at different time (14-29 d for LP2, 14-43 d for LP3). Samples were collected at 52 d of duck age. Sternal calcification analysis showed no significant difference in proportion of area of cartilage matrix and trabecular bone in keel tissue among the 3 groups, but the degree of keel calcification in LP3 was higher than in the other 2 groups. Serum metabolomics showed 32 and 28 differentially accumulated metabolites (DAMs) in the 2 comparison groups, LP1 vs. LP3 and LP1 vs. LP2, respectively. Carboxylic acids and derivatives were the most abundant among the DAMs. Sternal transcriptome analysis showed 231 differentially expressed genes (DEGs), including 177 upregulated genes and 54 downregulated genes in group LP1 vs. LP3, and 22 DEGs in group LP1 vs. LP2. Protein-protein interaction (PPI) network analysis on DEGs between LP1 and LP3 showed that genes BTRC, GLI1, BMP4, and FOS were in the core position of the interaction network, and are also involved in bone development. KEGG pathway analysis of DAMs and DEGs showed that differences in Hedgehog signaling pathway, MAPK signaling pathway, apoptosis, energy metabolism, and amino acid metabolism following light treatment seem likely to have contributed to the observed difference in calcification of duck sternum.
骨钙化是鸟类骨骼发育的关键过程,对于维持骨骼的正常生物学功能非常重要。光是影响骨骼发育的重要因素之一,但光照强度是否影响骨钙化以及其潜在机制尚不清楚。本研究以鸭胸骨为模型,分析了不同光照制度下的钙化过程。此外,还通过整合代谢组学和转录组学方法阐明了潜在的机制。实验从鸭龄 14 天持续到 51 天。对照组(LP1)在整个实验过程中保持光照强度 2 lx。两个光照补充组(LP2、LP3)在不同时间(LP2 为 14-29 天,LP3 为 14-43 天)给予光照强度为 70 lx。在鸭龄 52 天时收集样本。胸骨钙化分析显示,3 组鸭龙骨组织中软骨基质和小梁骨的面积比例无显著差异,但 LP3 组龙骨的钙化程度高于其他 2 组。血清代谢组学分析显示,在 LP1 与 LP3 和 LP1 与 LP2 的 2 个比较组中,分别有 32 个和 28 个差异积累代谢物(DAMs)。DAMs 中羧酸及其衍生物含量最丰富。胸骨转录组分析显示,LP1 与 LP3 组有 231 个差异表达基因(DEGs),包括 177 个上调基因和 54 个下调基因,LP1 与 LP2 组有 22 个 DEGs。LP1 与 LP3 组 DEGs 的蛋白质-蛋白质相互作用(PPI)网络分析显示,BTRC、GLI1、BMP4 和 FOS 基因处于相互作用网络的核心位置,它们也参与了骨骼发育。DAMs 和 DEGs 的 KEGG 通路分析显示,光照处理后 Hedgehog 信号通路、MAPK 信号通路、细胞凋亡、能量代谢和氨基酸代谢的差异可能导致鸭胸骨钙化的差异。