Wang Laidi, Hu Xiaodan, Wang Shasha, Yuan Chunyou, Wang Zhixiu, Chang Guobin, Chen Guohong
Key Laboratory of Animal Genetics and Breeding and Molecular Design of Jiangsu Province, Yangzhou University, Yangzhou 225009, China.
Anim Biosci. 2022 Sep;35(9):1327-1339. doi: 10.5713/ab.21.0441. Epub 2022 Jan 21.
Fat deposition in poultry is an important factor in production performance and meat quality research. miRNAs also play important roles in regulating adipocyte differentiation process. This study was to investigate the expression patterns of miRNAs in duck adipocytes after differentiation and explore the role of miR-214 in regulating carnitine palmitoyltransferases 2 (CPT2) gene expression during duck adipocyte differentiation.
Successful systems for the isolation, culture, and induction of duck primary fat cells was developed in the experiment. Using Illumina next-generation sequencing, the miRNAs libraries of duck adipocytes were established. miRanda was used to predict differentially expressed (DE) miRNAs and their target genes. The expression patterns of miR-214 and CPT2 during the differentiation were verified by quantitative real-time polymerase chain reaction and western blot. Luciferase reporter assays were used to explore the specific regions of CPT2 targeted by miR-214. We used a miR-214 over-expression strategy in vitro to further investigate its effect on differentiation process and CPT2 gene transcription.
There were 481 miRNAs identified in duck adipocytes, included 57 DE miRNA candidates. And the 1,046 targets genes of DE miRNAs were mainly involved in p53 signaling, FoxO signaling, and fatty acid metabolism pathways. miR-214 and CPT2 showed contrasting expression patterns before and after differentiation, and they were selected for further research. The expression of miR-214 was decreased during the first 3 days of duck adipocytes differentiation, and then increased, while the expression of CPT2 increased both in the transcriptional and protein level. The luciferase assay suggested that miR-214 targets the 3'untranslated region of CPT2. Overexpression of miR-214 not only promoted the formation of lipid droplets but also decreased the protein abundance of CPT2.
Current study reports the expression profile of miRNAs in duck adipocytes differentiated for 4 days. And miR-214 has been proved to have the regulator potential for fat deposition in duck.
家禽脂肪沉积是生产性能和肉质研究中的一个重要因素。微小RNA(miRNA)在调节脂肪细胞分化过程中也发挥着重要作用。本研究旨在调查鸭脂肪细胞分化后miRNA的表达模式,并探讨miR-214在鸭脂肪细胞分化过程中对肉碱棕榈酰转移酶2(CPT2)基因表达的调控作用。
实验中建立了成功的鸭原代脂肪细胞分离、培养和诱导体系。利用Illumina下一代测序技术,构建了鸭脂肪细胞的miRNA文库。使用miRanda预测差异表达(DE)miRNA及其靶基因。通过定量实时聚合酶链反应和蛋白质印迹法验证miR-214和CPT2在分化过程中的表达模式。利用荧光素酶报告基因检测法探索miR-214靶向CPT2的特定区域。我们在体外采用miR-214过表达策略,进一步研究其对分化过程和CPT2基因转录的影响。
在鸭脂肪细胞中鉴定出481个miRNA,其中包括57个DE miRNA候选物。DE miRNA的1046个靶基因主要参与p53信号通路、FoxO信号通路和脂肪酸代谢途径。miR-214和CPT2在分化前后呈现出相反的表达模式,因此选择它们进行进一步研究。在鸭脂肪细胞分化的前3天,miR-214的表达下降,然后升高,而CPT2在转录和蛋白质水平上均升高。荧光素酶检测表明,miR-214靶向CPT2的3'非翻译区。miR-214的过表达不仅促进了脂滴的形成,还降低了CPT2的蛋白质丰度。
本研究报道了分化4天的鸭脂肪细胞中miRNA的表达谱。并且已证明miR-214对鸭脂肪沉积具有调节潜力。