Jiao Lefei, Dai Tianmeng, Sun Peng, Jin Min, Zhou Qicun
Laboratory of Fish Nutrition, School of Marine Sciences, Ningbo University, Ningbo 315211, China.
Animals (Basel). 2021 Oct 4;11(10):2893. doi: 10.3390/ani11102893.
Aryl hydrocarbon receptor nuclear translocator-like protein 1 (BMAL1) is a core circadian transcription factor that controls the 24-h cycle of physiological processes. In shrimp, the role of BMAL1 in the regulating glucose metabolism remains unclear. Firstly, we observed that the daily profile of BMAL1, GLUT1 and SGLT1 expression were synchronized in the intestine and the hepatopancreas of . Then we examined the effects of BMAL1 on the gene expression of glucose transporter type 1 (SGLT1) and sodium-glucose cotransporter 1 (GLUT1) in vivo and in vitro. BMAL1 in shares 70.91-96.35% of sequence identities with other shrimp species and possesses the conserved helix-loop-helix domain and polyadenylation site domain. The in vitro dual-luciferase reporter assay and in vivo RNA interference experiment demonstrated that BMAL1 exerted a positive regulation effect on the expression of glucose transporters in . Moreover, we conducted an eight-week treatment to investigate whether light/dark cycle change would influence growth performance, and gene expression of BMAL1, GLUT1 and SGLT1 in . Our result showed that compared with natural light treatment, constant darkness (24-h darkness) significantly decreased ( < 0.05) serum glucose concentration, and suppressed ( < 0.05) the gene expression of BMAL1, GLUT1 and SGLT1 in the hepatopancreas and the intestine. Growth performance and survival rate were also decreased ( < 0.05) by constant darkness treatment. Our result identified BMAL1 as a critical mediator regulating the expression of glucose transporters, which could be suppressed by constant darkness in It would be quite interesting to explore the mechanism of dark/light cycles on glucose transport and metabolism in which might provide a feeding strategy for improving carbohydrate utilization in the future.
芳烃受体核转运蛋白样蛋白1(BMAL1)是一种核心昼夜节律转录因子,控制着生理过程的24小时循环。在虾中,BMAL1在调节葡萄糖代谢中的作用仍不清楚。首先,我们观察到BMAL1、葡萄糖转运蛋白1(GLUT1)和钠葡萄糖协同转运蛋白1(SGLT1)在虾的肠道和肝胰腺中的每日表达谱是同步的。然后,我们在体内和体外研究了BMAL1对葡萄糖转运蛋白1(SGLT1)和钠葡萄糖协同转运蛋白1(GLUT1)基因表达的影响。虾中的BMAL1与其他虾类物种的序列同一性为70.91 - 96.35%,并具有保守的螺旋-环-螺旋结构域和聚腺苷酸化位点结构域。体外双荧光素酶报告基因检测和体内RNA干扰实验表明,BMAL1对虾中葡萄糖转运蛋白的表达具有正向调节作用。此外,我们进行了为期八周的处理,以研究光/暗周期变化是否会影响虾的生长性能以及BMAL1、GLUT1和SGLT1的基因表达。我们的结果表明,与自然光处理相比,持续黑暗(24小时黑暗)显著降低(P < 0.05)了血清葡萄糖浓度,并抑制(P < 0.05)了肝胰腺和肠道中BMAL1、GLUT1和SGLT1的基因表达。持续黑暗处理也降低(P < 0.05)了生长性能和存活率。我们的结果确定BMAL1是调节葡萄糖转运蛋白表达的关键介质,持续黑暗可抑制虾中的这种调节作用。探索光/暗周期对虾葡萄糖转运和代谢的影响机制将非常有趣,这可能为未来提高碳水化合物利用率提供一种投喂策略。