Chun Rene F, Blatter Elizabeth, Elliott Stephanie, Fitz-Gibbon Sorel, Rieger Sandra, Sagasti Alvaro, Adams John S, Hewison Martin
Department of Orthopaedic Surgery, UCLA-Orthopaedic Hospital, Los Angeles, CA, 90095, United States.
Cell Biochem Funct. 2014 Dec;32(8):675-82. doi: 10.1002/cbf.3071. Epub 2014 Oct 7.
Activation of precursor 25-hydroxyvitamin D3 (25D) to hormonal 1,25-dihydroxyvitamin D3 (1,25D) is a pivotal step in vitamin D physiology, catalysed by the enzyme 25-hydroxyvitamin D-1α-hydroxylase (1α-hydroxylase). To establish new models for assessing the physiological importance of the 1α-hydroxylase-25D-axis, we used Danio rerio (zebrafish) to characterize expression and biological activity of the gene for 1α-hydroxylase (cyp27b1). Treatment of day 5 zebrafish larvae with inactive 25D (5-150 nM) or active 1,25D (0.1-10 nM) induced dose responsive expression (15-95-fold) of the vitamin D-target gene cyp24a1 relative to larvae treated with vehicle, suggesting the presence of Cyp27b1 activity. A full-length zebrafish cyp27b1 cDNA was then generated using RACE and RT-PCR methods. Sequencing of the resulting clone revealed an open reading frame encoding a protein of 505 amino acids with 54% identity to human CYP27B1. Transfection of a cyp27b1 expression vector into HKC-8, a human kidney proximal tubular epithelial cell line, enhanced intracrine metabolism of 25D to 1,25D resulting in greater than twofold induction of CYP24A1 mRNA expression and a 25-fold increase in 1,25D production compared to empty vector. These data indicate that we have cloned a functional zebrafish CYP27B1, representing a phylogenetically distant branch from mammals of this key enzyme in vitamin D metabolism. Further analysis of cyp27b1 expression and activity in zebrafish may provide new perspectives on the biological importance of 25D metabolism.
前体25-羟基维生素D3(25D)活化为激素1,25-二羟基维生素D3(1,25D)是维生素D生理学中的关键步骤,由25-羟基维生素D-1α-羟化酶(1α-羟化酶)催化。为了建立评估1α-羟化酶-25D轴生理重要性的新模型,我们使用斑马鱼来表征1α-羟化酶(cyp27b1)基因的表达和生物学活性。用无活性的25D(5-150 nM)或活性1,25D(0.1-10 nM)处理第5天的斑马鱼幼虫,相对于用赋形剂处理的幼虫,诱导维生素D靶基因cyp24a1的剂量反应性表达(15-95倍),表明存在Cyp27b1活性。然后使用RACE和RT-PCR方法生成全长斑马鱼cyp27b1 cDNA。对所得克隆进行测序,发现一个开放阅读框,编码一个505个氨基酸的蛋白质,与人CYP27B1有54%的同一性。将cyp27b1表达载体转染到人肾近端小管上皮细胞系HKC-8中,增强了25D向1,25D的内分泌代谢,导致CYP24A1 mRNA表达诱导超过两倍,1,25D产量增加25倍,与空载体相比。这些数据表明我们已经克隆了一种功能性斑马鱼CYP27B1,它代表了维生素D代谢中这种关键酶在系统发育上与哺乳动物相距遥远的一个分支。对斑马鱼中cyp27b1表达和活性的进一步分析可能会为25D代谢的生物学重要性提供新的视角。