Bou Marta, Montfort Jerôme, Le Cam Aurélie, Rallière Cécile, Lebret Véronique, Gabillard Jean-Charles, Weil Claudine, Gutiérrez Joaquim, Rescan Pierre-Yves, Capilla Encarnación, Navarro Isabel
Department of Cell Biology, Physiology and Immunology, Faculty of Biology, University of Barcelona, Av. Diagonal 643, 08028, Barcelona, Spain.
Present address: Nofima (Norwegian Institute of Food, Fisheries, and Aquaculture Research), P.O. Box 210, N-1432, Ås, Norway.
BMC Genomics. 2017 May 4;18(1):347. doi: 10.1186/s12864-017-3728-0.
Excessive accumulation of adipose tissue in cultured fish is an outstanding problem in aquaculture. To understand the development of adiposity, it is crucial to identify the genes which expression is associated with adipogenic differentiation. Therefore, the transcriptomic profile at different time points (days 3, 8, 15 and 21) along primary culture development of rainbow trout preadipocytes has been investigated using an Agilent trout oligo microarray.
Our analysis identified 4026 genes differentially expressed (fold-change >3) that were divided into two major clusters corresponding to the main phases observed during the preadipocyte culture: proliferation and differentiation. Proliferation cluster comprised 1028 genes up-regulated from days 3 to 8 of culture meanwhile the differentiation cluster was characterized by 2140 induced genes from days 15 to 21. Proliferation was characterized by enrichment in genes involved in basic cellular and metabolic processes (transcription, ribosome biogenesis, translation and protein folding), cellular remodelling and autophagy. In addition, the implication of the eicosanoid signalling pathway was highlighted during this phase. On the other hand, the terminal differentiation phase was enriched with genes involved in energy production, lipid and carbohydrate metabolism. Moreover, during this phase an enrichment in genes involved in the formation of the lipid droplets was evidenced as well as the activation of the thyroid-receptor/retinoic X receptor (TR/RXR) and the peroxisome proliferator activated receptors (PPARs) signalling pathways. The whole adipogenic process was driven by a coordinated activation of transcription factors and epigenetic modulators.
Overall, our study demonstrates the coordinated expression of functionally related genes during proliferation and differentiation of rainbow trout adipocyte cells. Furthermore, the information generated will allow future investigations of specific genes involved in particular stages of fish adipogenesis.
养殖鱼类脂肪组织过度积累是水产养殖中的一个突出问题。为了解肥胖的发展过程,识别与脂肪生成分化相关的基因表达至关重要。因此,利用安捷伦鲑鱼寡核苷酸微阵列研究了虹鳟鱼前脂肪细胞原代培养过程中不同时间点(第3、8、15和21天)的转录组图谱。
我们的分析确定了4026个差异表达基因(倍数变化>3),这些基因分为两个主要簇,对应于前脂肪细胞培养过程中观察到的主要阶段:增殖和分化。增殖簇包含1028个在培养第3天到第8天上调的基因,而分化簇的特征是在第15天到第21天有2140个诱导基因。增殖的特征是参与基本细胞和代谢过程(转录、核糖体生物合成、翻译和蛋白质折叠)、细胞重塑和自噬的基因富集。此外,在这个阶段类花生酸信号通路的作用也得到了突出体现。另一方面,终末分化阶段富含参与能量产生、脂质和碳水化合物代谢的基因。此外,在这个阶段还证明了参与脂滴形成的基因富集以及甲状腺受体/视黄酸X受体(TR/RXR)和过氧化物酶体增殖物激活受体(PPARs)信号通路的激活。整个脂肪生成过程由转录因子和表观遗传调节剂的协同激活驱动。
总体而言,我们的研究证明了虹鳟鱼脂肪细胞增殖和分化过程中功能相关基因的协同表达。此外,所产生的信息将有助于未来对鱼类脂肪生成特定阶段涉及的特定基因进行研究。