Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, College of Fisheries, Southwest University, Chongqing, China.
Key Laboratory of Sichuan Province for Fishes Conservation and Utilization in the Upper Reaches of the Yangtze River, Neijiang Normal University, Neijiang, China.
Comp Biochem Physiol A Mol Integr Physiol. 2024 Jan;287:111523. doi: 10.1016/j.cbpa.2023.111523. Epub 2023 Oct 4.
The dysregulation of glucose-G6P (glucose-6-phosphate) interconversion is thought to be one of the main reasons for the low glucose disposal of carnivorous fish, but is not yet well understood in largemouth bass Micropterus salmoides (LMB). In this study, the full length cDNA sequences of genes encoding glucokinase (Gck, catalyzing glucose phosphorylation) and glucose-6-phosphatase catalytic subunit (G6pc, catalyzing glucose dephosphorylation) were cloned by the RACE method from the liver of LMB. Subsequently, the distribution of g6pc and gck as well as their transcriptional regulation by dietary starch levels and a glucose load were investigated. Only one gck gene was identified, while the tandem duplication of g6pca.1 gene was named as g6pca.2 in LMB. The full cDNA sequences of g6pca.1, g6pca.2 and gck in LMB were 1585, 1813 and 2115 bp in length, encoding 478, 352 and 359 amino acids, respectively. Gck was predicted to contain two hexokinase domains, an ATP-binding domain and multiple functional sites, while G6pca.1 and G6pca.2 contained nine transmembrane helices, a PAP2 (type-2 phosphatidic acid phosphatase) domain and multiple functional amino acid sites. Both g6pca.1 and g6pca.2 were predominantly distributed in the liver and to some extent in the intraperitoneal fat, intestine and pyloric caeca, while gck was mainly transcribed in the liver and to some extent in the heart, intestine and brain. Both feeding a high starch diet and a glucose load stimulated the mRNA expression of gck in the liver of LMB. An increase of dietary starch from 9% to 14% down-regulated the transcription of g6pca.1 in the liver of LMB. However, both the mRNA levels of hepatic g6pca.1 and g6pca.2 were sharply up-regulated in LMB during 1-3 h after a glucose load. Overall, the results of this study suggested that the functions of G6pc (G6pca.1 and G6pca.2) and Gck in LMB were highly conserved in evolution. Though hepatic glucose-G6P interconversion was well regulated at the transcript level in LMB fed high starch diets, a futile cycle between glucose and G6P was induced in the liver after a glucose load.
葡萄糖-G6P(葡萄糖-6-磷酸)互变的失调被认为是肉食性鱼类葡萄糖摄取率低的主要原因之一,但在大口黑鲈(Micropterus salmoides)中尚未得到很好的理解。在本研究中,采用 RACE 方法从大口黑鲈肝脏中克隆了编码葡萄糖激酶(Gck,催化葡萄糖磷酸化)和葡萄糖-6-磷酸酶催化亚基(G6pc,催化葡萄糖去磷酸化)的基因的全长 cDNA 序列。随后,研究了 g6pc 和 gck 的分布及其受膳食淀粉水平和葡萄糖负荷的转录调控。结果仅鉴定出一个 gck 基因,而 g6pca.1 基因的串联重复则被命名为 LMB 中的 g6pca.2。LMB 中 g6pca.1、g6pca.2 和 gck 的全长 cDNA 序列分别为 1585、1813 和 2115bp,分别编码 478、352 和 359 个氨基酸。Gck 被预测含有两个己糖激酶结构域、一个 ATP 结合结构域和多个功能位点,而 G6pca.1 和 G6pca.2 含有 9 个跨膜螺旋、一个 PAP2(2 型磷酸脂酶)结构域和多个功能氨基酸位点。g6pca.1 和 g6pca.2 主要分布于肝脏,并在一定程度上分布于腹腔脂肪、肠和幽门盲囊,而 gck 主要转录于肝脏,并在一定程度上转录于心脏、肠和脑。高淀粉饮食和葡萄糖负荷均能刺激大口黑鲈肝脏中 gck 的 mRNA 表达。LMB 肝脏中 g6pca.1 的转录水平从 9%到 14%的淀粉水平降低。然而,在葡萄糖负荷后 1-3h,LMB 肝脏中 g6pca.1 和 g6pca.2 的 mRNA 水平均急剧上调。总体而言,本研究结果表明,G6pc(g6pca.1 和 g6pca.2)和 Gck 在大口黑鲈中的功能在进化上高度保守。尽管在高淀粉饮食喂养的大口黑鲈中,肝内葡萄糖-G6P 互变在转录水平上得到了很好的调节,但在葡萄糖负荷后,肝内葡萄糖和 G6P 之间会产生无效循环。