Raikwar Nandita S, Thomas Christie P
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa.
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa
Physiol Rep. 2017 Apr;5(7). doi: 10.14814/phy2.13221.
We previously identified a 5' variant alternate transcript of Sgk1 (Sgk1_v3) encoding an NH-terminal variant Sgk1 isoform, Sgk1_i3 that, like Sgk1, is expressed in the distal convoluted tubule, connecting tubule and collecting duct and can stimulate epithelial Na transport (Am J Physiol Renal Physiol 303: F1527-F1533, 2012). We now demonstrate that, similar to Sgk1, aldosterone and glucocorticoids stimulate Sgk1_v3 expression in cell lines from the collecting duct and airway epithelia. In mice, short term aldosterone infusion and maneuvers that increase endogenous aldosterone secretion including dietary Na deprivation and K loading increases distal nephron Sgk1_v3 expression in vivo. Although Sgk1_v3 has a different 5' proximal regulatory region from Sgk1, the transcription start sites are less than 1000 bp apart. We cloned the 5' regulatory region for Sgk1 and Sgk_v3 upstream of a luciferase gene and by deletion and reporter gene analysis we localized the corticosteroid regulatory region for Sgk1_v3 to a glucocorticoid response element (GRE) that had previously been identified for Sgk1 (Am J Physiol Endo Metab 283: E971-E979, 2002). We tested this element with MR in an MR-null cell line and demonstrate that aldosterone stimulates Sgk1 and Sgk1_v3 via this GRE We conclude that corticosteroids stimulate Sgk1 and Sgk1_v3 expression in epithelial cells via activation of a common conserved GRE in the 5' flanking region of Sgk1.
我们之前鉴定出了Sgk1的一种5'端可变转录本(Sgk1_v3),其编码一种N端可变Sgk1亚型Sgk1_i3。与Sgk1一样,Sgk1_i3在远曲小管、连接小管和集合管中表达,并且能够刺激上皮钠转运(《美国生理学杂志:肾脏生理学》303卷:F1527 - F1533,2012年)。我们现在证明,与Sgk1相似,醛固酮和糖皮质激素可刺激来自集合管和气道上皮的细胞系中Sgk1_v3的表达。在小鼠中,短期输注醛固酮以及包括饮食中钠缺乏和钾负荷增加等可增加内源性醛固酮分泌的操作,均可在体内增加远端肾单位Sgk1_v3的表达。尽管Sgk1_v3与Sgk1有不同的5'近端调控区域,但转录起始位点相距不到1000 bp。我们在荧光素酶基因上游克隆了Sgk1和Sgk_v3的5'调控区域,并通过缺失和报告基因分析,将Sgk1_v3的皮质类固醇调控区域定位到一个先前已鉴定出的Sgk1的糖皮质激素反应元件(GRE)(《美国生理学杂志:内分泌与代谢》283卷:E971 - E979,2002年)。我们在一个缺乏MR的细胞系中用MR对该元件进行了测试,并证明醛固酮通过这个GRE刺激Sgk1和Sgk1_v3。我们得出结论,皮质类固醇通过激活Sgk1 5'侧翼区域中一个共同的保守GRE来刺激上皮细胞中Sgk1和Sgk1_v3的表达。