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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Fatty acid synthase promoter: Characterization, and transcriptional regulation by sterol regulatory element binding protein-1 in goat mammary epithelial cells
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Fatty acid synthase promoter: Characterization, and transcriptional regulation by sterol regulatory element binding protein-1 in goat mammary epithelial cells

机译:脂肪酸合酶启动子:山羊乳腺上皮细胞中固醇调节元件结合蛋白-1的表征和转录​​调控

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Fatty acid synthase (FASN) is the central enzyme of the de novo fatty acid biosynthesis pathway. Although the FASN transcriptional regulatory mechanism has been elucidated clearly in many tumor cells, its mechanism is still not clear in the ruminant mammary gland. In this study, we cloned and sequenced a 1.8-kb fragment of the FASN 5 ' flanking region from goat genomic DNA Multiple alignment analysis demonstrated that the entire 1.8-kb fragment has little homology but that the sub-section nearest the transcriptional start site (-203 to +1) is more conserved across species, in particular the binding motifs for transcriptional regulation. Deletion analysis revealed a putative core promoter region located in -297/-14 bp upstream of the transcription site within the high homology domain. Mutations of sterol response elements (SRE1 and SRE2) and the nuclear factor Y (NF-Y) binding site appeared to significantly down-regulate the FASN promoter activity in goat mammary epithelial cells (P < 0.05). Further analysis showed that both SRE sites responded to sterol regulatory element-binding protein 1 (SREBP-1). SREBP-1 overexpression and knockdown by small interference RNA influenced the abundance of endogenous FASN. These data suggested that SREBP-1 may regulate FASN expression at the transcriptional level in the lactating goat mammary gland. Hence, the current work will contribute valuable information to understanding the molecular regulatory mechanisms of FASN during lactation. (C) 2015 Published by Elsevier B.V.
机译:脂肪酸合酶(FASN)是从头脂肪酸生物合成途径的中心酶。尽管已在许多肿瘤细胞中清楚阐明了FASN转录调控机制,但在反刍动物的乳腺中其机制仍不清楚。在这项研究中,我们从山羊基因组DNA中克隆了FASN 5'侧翼区的1.8kb片段并对其进行了测序。多重比对分析表明,整个1.8kb片段几乎没有同源性,但最靠近转录起始位点的小部分( -203至+1)在物种间更保守,尤其是转录调控的结合基序。缺失分析显示推定的核心启动子区域位于高同源性域内转录位点上游-297 / -14 bp。固醇反应元件(SRE1和SRE2)和核因子Y(NF-Y)结合位点的突变似乎显着下调了山羊乳腺上皮细胞的FASN启动子活性(P <0.05)。进一步的分析表明,两个SRE位点都对固醇调节元件结合蛋白1(SREBP-1)产生反应。 SREBP-1的过表达和小干扰RNA的敲低影响了内源性FASN的丰度。这些数据表明,SREBP-1可能在哺乳山羊乳腺的转录水平上调节FASN表达。因此,当前的工作将为了解泌乳期FASN的分子调控机制提供有价值的信息。 (C)2015由Elsevier B.V.发布

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