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KLF6是一种参与调节酸性神经酰胺酶基因表达的转录因子。

KLF6 is one transcription factor involved in regulating acid ceramidase gene expression.

作者信息

Park Jae-Ho, Eliyahu Efrat, Narla Goutham, DiFeo Analisa, Martignetti John A, Schuchman Edward H

机构信息

Departments of Human Genetics, Mount Sinai School of Medicine, 1425 Madison Avenue, New York, NY 10029, USA.

出版信息

Biochim Biophys Acta. 2005 Dec 30;1732(1-3):82-7. doi: 10.1016/j.bbaexp.2006.01.002. Epub 2006 Jan 26.

Abstract

Acid ceramidase (AC; E.C.3.5.1.23) activity is required to hydrolyze ceramide into sphingosine. An inherited deficiency of this enzymatic activity leads to the lipid storage disorder, Farber Lipogranulomatosis. Aberrant AC activity also has been demonstrated in several human cancers. We have characterized a 1931-bp putative promoter region of the murine AC gene by Luciferase reporter assays, electrophoretic mobility shift assays, and mutational analysis. A 143-bp sequence essential for AC promoter activity was found, and mobility shift and super-shift experiments using nuclear extracts of NIH3T3 cells demonstrated that a 34-bp, GC-rich sub-region could bind the transcription factors KLF6, Sp1, and AP2. Transient over-expression of KLF6 in NIH3T3 cells significantly increased the activity of a co-transfected Luciferase reporter construct containing the wild-type AC promoter, and a positive correlation was observed between AC and KFL6 RNA and protein expression in two different human cancer cell lines in which KLF6 expression was either "knocked-down" by RNAi or increased by retroviral-mediated gene transfer. Northern blot analysis also revealed a correlation of KLF6 and AC gene expression in various human tissues. These results provide the first characterization of the AC promoter from any species and demonstrate that KLF6 is one transcription factor involved in the regulation of AC gene expression.

摘要

酸性神经酰胺酶(AC;E.C.3.5.1.23)活性是将神经酰胺水解为鞘氨醇所必需的。这种酶活性的遗传性缺乏会导致脂质贮积病——法伯脂肪肉芽肿病。在几种人类癌症中也已证实存在异常的AC活性。我们通过荧光素酶报告基因检测、电泳迁移率变动分析和突变分析,对小鼠AC基因1931 bp的假定启动子区域进行了表征。发现了一个对AC启动子活性至关重要的143 bp序列,使用NIH3T3细胞的核提取物进行的迁移率变动和超迁移实验表明,一个富含GC的34 bp子区域可以结合转录因子KLF6、Sp1和AP2。在NIH3T3细胞中瞬时过表达KLF6可显著增加共转染的含有野生型AC启动子的荧光素酶报告基因构建体的活性,并且在两种不同的人类癌细胞系中,当KLF6表达通过RNAi“敲低”或通过逆转录病毒介导的基因转移增加时,观察到AC与KFL6的RNA和蛋白质表达之间呈正相关。Northern印迹分析还揭示了KLF6与AC基因在各种人类组织中的表达相关性。这些结果首次对任何物种的AC启动子进行了表征,并证明KLF6是参与调节AC基因表达 的一种转录因子。

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