Du Xiaofei, Rosenfield Robert L, Qin Kenan
Section of Pediatric Endocrinology, 5839 South Maryland Avenue, MC 5053, Chicago, Illinois 60637, USA.
J Clin Endocrinol Metab. 2009 Jul;94(7):2594-601. doi: 10.1210/jc.2009-0139. Epub 2009 Apr 14.
Kruppel-like factor 15 (KLF15) is a newly discovered transcription factor that plays an important role in glucose homeostasis and lipid accumulation in cells. We present evidence for KLF15 as a transcriptional regulator of the human 17beta-hydroxysteroid dehydrogenase type 5 gene (HSD17B5) and its potential role in the pathogenesis of hyperandrogenism.
The aim was to investigate the molecular mechanism of HSD17B5 regulation.
Diverse molecular biology techniques were used.
We identified a KLF15 binding site in the HSD17B5 promoter by using luciferase promoter constructs, EMSA, and chromatin immunoprecipitation assays. Overexpression of KLF15 increased HSD17B5 promoter activity and testosterone formation at least 3-fold in cultured H295R cells. Insulin increased KLF15 mRNA expression according to real-time RT-PCR and increased HSD17B5 promoter activity according to luciferase assays. KLF15 overexpression in combination with insulin, glucocorticoid, and cAMP stimulated adipogenesis in H295R cells. In silico and RT-PCR analyses showed that the KLF15 gene promoter undergoes alternative splicing in a tissue-specific manner. Comparison of the HSD17B5 promoter in seven different species revealed that the KLF15 binding site has no human homolog in species other than orangutans.
KLF15 is potentially a novel link between the regulation of testosterone production and fat stores by insulin in humans.
Kruppel样因子15(KLF15)是一种新发现的转录因子,在细胞葡萄糖稳态和脂质积累中发挥重要作用。我们提供证据表明KLF15是人类5型17β-羟类固醇脱氢酶基因(HSD17B5)的转录调节因子,及其在高雄激素血症发病机制中的潜在作用。
旨在研究HSD17B5调控的分子机制。
使用了多种分子生物学技术。
我们通过荧光素酶启动子构建体、电泳迁移率变动分析(EMSA)和染色质免疫沉淀分析,在HSD17B5启动子中鉴定出一个KLF15结合位点。在培养的H295R细胞中,KLF15的过表达使HSD17B5启动子活性和睾酮生成增加至少3倍。根据实时逆转录PCR,胰岛素增加KLF15 mRNA表达;根据荧光素酶分析,胰岛素增加HSD17B5启动子活性。KLF15过表达与胰岛素、糖皮质激素和cAMP联合刺激H295R细胞的脂肪生成。计算机分析和逆转录PCR分析表明,KLF15基因启动子以组织特异性方式进行可变剪接。对七个不同物种的HSD17B5启动子进行比较,发现除猩猩外,KLF15结合位点在其他物种中没有人类同源物。
KLF15可能是人类胰岛素调节睾酮产生和脂肪储存之间的新联系。