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miR-146a 通过靶向 elovl5 参与调控脊椎动物 LC-PUFA 生物合成,这在兔鱼 Siganus canaliculatus 中得到了证实。

miR-146a is involved in the regulation of vertebrate LC-PUFA biosynthesis by targeting elovl5 as demonstrated in rabbitfish Siganus canaliculatus.

机构信息

Guangdong Provincial Key Laboratory of Marine Biotechnology, Shantou University, Shantou, China.

Guangdong Provincial Key Laboratory of Marine Biotechnology, Shantou University, Shantou, China.

出版信息

Gene. 2018 Nov 15;676:306-314. doi: 10.1016/j.gene.2018.08.063. Epub 2018 Aug 23.

DOI:10.1016/j.gene.2018.08.063
PMID:30145362
Abstract

Rabbitfish Siganus canaliculatus is the first marine teleost demonstrated to have the ability to synthesize long-chain polyunsaturated fatty acids (LC-PUFA) from C PUFA precursors, and thus provides us a unique model for studying the regulatory mechanisms of LC-PUFA biosynthesis in teleosts. MicroRNAs (miRNAs) were shown to play important roles in the regulation of LC-PUFA biosynthesis in rabbitfish at posttranscriptional level in our previous studies. Here, we focused the roles of miR-146a in such regulation. The expression of miR-146a displayed an inverse pattern with that of elongase 5 (Elovl5), a key enzyme catalyzing the elongation of C (18:4n3 and 18:3n6) and C (20:5n3 and 20:4n6) PUFA in the LC-PUFA biosynthesis, in vivo in liver of rabbitfish reared under different salinities, as well as in vitro in S. canaliculatus hepatocyte line (SCHL) cells incubated with different fatty acids. Bioinformatics analysis predicted that miR-146a may target the 3'UTR of elovl5 directly, which was confirmed by the dual luciferase reporter assays in HEK 293T cells. Overexpression of miR-146a significantly downregulated the expression of elovl5 in SCHL cells, while knockdown of miR-146a showed an opposite effect. Moreover, up-regulation of miR-146a in SCHL cells significantly suppressed the elongation indexes 20:3n6/18:3n6, 20:4n3/18:4n3 and 22:5n3/20:5n3 associated with Elovl5 catalyzing activity, and consequently reduced the contents of LC-PUFA. These results indicate that miR-146a is involved in the regulation of LC-PUFA biosynthesis through inhibiting the mRNA expression and activity of Elovl5 in rabbitfish, which was for the first time to focus on the role of miR-146a in LC-PUFA biosynthesis in vertebrates and will provide a new insight into the regulatory mechanisms of LC-PUFA biosynthesis in teleosts.

摘要

条纹鲷(Siganus canaliculatus)是第一个被证明具有从 C 型多不饱和脂肪酸(C PUFA)前体合成长链多不饱和脂肪酸(LC-PUFA)能力的海洋硬骨鱼,这为我们研究硬骨鱼 LC-PUFA 生物合成的调控机制提供了一个独特的模型。在我们之前的研究中,miRNAs(miRNAs)被证明在条纹鲷 LC-PUFA 生物合成的转录后水平发挥重要作用。在这里,我们重点研究了 miR-146a 在这种调控中的作用。miR-146a 的表达与延长酶 5(Elovl5)的表达呈相反模式,Elovl5 是 LC-PUFA 生物合成中催化 C(18:4n3 和 18:3n6)和 C(20:5n3 和 20:4n6)PUFA 延长的关键酶,在不同盐度下饲养的条纹鲷肝脏体内以及用不同脂肪酸孵育的条纹鲷肝细胞系(SCHL)细胞体外均如此。生物信息学分析预测 miR-146a 可能直接靶向 elovl5 的 3'UTR,这在 HEK 293T 细胞中的双荧光素酶报告基因实验中得到了证实。miR-146a 的过表达显著下调了 SCHL 细胞中 elovl5 的表达,而 miR-146a 的敲低则表现出相反的效果。此外,miR-146a 在 SCHL 细胞中的上调显著抑制了与 Elovl5 催化活性相关的 20:3n6/18:3n6、20:4n3/18:4n3 和 22:5n3/20:5n3 的延长指数,并因此降低了 LC-PUFA 的含量。这些结果表明,miR-146a 通过抑制条纹鲷 Elovl5 的 mRNA 表达和活性参与 LC-PUFA 生物合成的调控,这是首次关注 miR-146a 在脊椎动物 LC-PUFA 生物合成中的作用,并将为硬骨鱼 LC-PUFA 生物合成的调控机制提供新的见解。

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