College of Marine Sciences of South China Agricultural University & Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510642, China.
Laboratory of Aquatic Animal Nutrition and Diet, College of Fisheries, Henan Normal University, Xinxiang 453007, China.
Int J Mol Sci. 2020 Jul 3;21(13):4736. doi: 10.3390/ijms21134736.
Omega-3 long chain polyunsaturated fatty acids (n-3 LC-PUFA), particularly docosahexaenoic acids (22:6n-3, DHA), have positive effects on multiple biologic and pathologic processes. Fish are the major dietary source of n-3 LC-PUFA for humans. Growing evidence supports acyl-coenzyme A (acyl-CoA) synthetase 6 () being involved in cellular DHA uptake and lipogenesis in mammals, while its molecular function and regulatory mechanism remain unknown in fish. The present study focused on investigating the molecular characterization and transcription regulation of the gene in the freshwater teleost common carp (). First, the full length of cDNA contained a coding region of 2148 bp for 715 amino acids, which possessed all characteristic features of the acyl-CoA synthetase (ACSL) family. Its mRNA expression was the highest in the brain, followed by in the heart, liver, kidney, muscle, and eyes, but little expression was detected in the ovary and gills. Additionally, a candidate promoter region of 2058 bp was cloned, and the sequence from -758 bp to -198 bp was determined as core a promoter by equal progressive deletion and electrophoretic mobility shift assay. The binding sites for important transcription factors (TFs), including stimulatory protein 1 (SP1), CCAAT enhancer-binding protein (C/EBPα), sterol-regulatory element binding protein 1c (SREBP1c), peroxisome proliferator activated receptor α (PPARα), and PPARγ were identified in the core promoter by site-directed mutation and functional assays. Furthermore, the intraperitoneal injection of PPARγ agonists (balaglitazone) increased the expression of mRNA, coupling with an increased proportion of DHA in the muscle, while opposite results were obtained in the injection of the SREBP1c antagonist (betulin). However, the expression of and DHA content in muscle were largely unchanged by PPARα agonist (fenofibrate) treatment. These results indicated that may play an important role for the muscular DHA uptake and deposition in common carp, and PPARγ and SREBP-1c are the potential TFs involved in the transcriptional regulation of gene. To our knowledge, this is the first report of the characterization of gene and its promoter in teleosts.
ω-3 长链多不饱和脂肪酸(n-3LC-PUFA),特别是二十二碳六烯酸(22:6n-3,DHA),对多种生物和病理过程有积极影响。鱼类是人类 n-3LC-PUFA 的主要膳食来源。越来越多的证据支持酰基辅酶 A(酰基辅酶 A)合成酶 6()参与哺乳动物细胞内 DHA 的摄取和脂肪生成,但其在鱼类中的分子功能和调节机制尚不清楚。本研究重点研究淡水鱼类鲤鱼()中基因的分子特征和转录调控。首先,全长 cDNA 包含一个编码 715 个氨基酸的 2148bp 编码区,具有酰基辅酶 A 合成酶(ACSL)家族的所有特征。其 mRNA 表达在脑中最高,其次是心脏、肝脏、肾脏、肌肉和眼睛,而在卵巢和鳃中几乎检测不到。此外,克隆了一个候选的 2058bp 启动子区域,通过等比例渐进缺失和电泳迁移率变动试验确定从-758bp 到-198bp 的序列为核心 a 启动子。通过定点突变和功能试验,在核心启动子中鉴定了重要转录因子(TFs)的结合位点,包括刺激蛋白 1(SP1)、CCAAT 增强子结合蛋白(C/EBPα)、固醇调节元件结合蛋白 1c(SREBP1c)、过氧化物酶体增殖物激活受体α(PPARα)和 PPARγ。此外,腹腔注射 PPARγ 激动剂(吡格列酮)增加了肌肉中 mRNA 的表达,同时肌肉中 DHA 的比例增加,而注射 SREBP1c 拮抗剂(桦木酸)则得到相反的结果。然而,PPARα 激动剂(非诺贝特)处理对肌肉中基因的表达和 DHA 含量影响不大。这些结果表明,在鲤鱼中,可能在肌肉中 DHA 的摄取和沉积中发挥重要作用,而 PPARγ 和 SREBP-1c 是参与基因转录调控的潜在 TF。据我们所知,这是首次报道鱼类中基因及其启动子的特征。