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骆驼FGF21基因功能启动子分析及靶向FGF21蛋白的小分子化合物鉴定

Analysis of Functional Promoter of Camel FGF21 Gene and Identification of Small Compounds Targeting FGF21 Protein.

作者信息

Yong Fang, Yan Meilin, Zhang Lili, Ji Wangye, Zhao Shuqin, Gao Yuan

机构信息

College of Life Science and Technology, Gansu Agricultural University, Lanzhou 730070, China.

Gansu Key Laboratory of Animal Generational Physiology and Reproductive Regulation, Lanzhou 730070, China.

出版信息

Vet Sci. 2023 Jul 10;10(7):452. doi: 10.3390/vetsci10070452.

Abstract

The fibroblast growth factor 21 (FGF21) gene plays an important role in the mechanism of glucose and lipid metabolism and is a promising therapeutic target for metabolic disease. Camels display a unique regulation characteristic of glucose and lipid metabolism, endowing them with the ability to adapt to survive drought and chronic hunger. However, the knowledge about the camel FGF21 gene regulation and its differences between humans and mice is still limited. In this study, camel FGF21 gene promoter was obtained for 2000 bp upstream of the transcriptional start site (TSS). Bioinformatics analysis showed that the proximal promoter region sequences near the TSS between humans and camels have high similarity. Two potential core active regions are located in the -445-612 bp region. In addition, camel FGF21 promoter contains three CpG islands (CGIs), located in the -435-1168 bp regions, significantly more and longer than in humans and mice. The transcription factor binding prediction showed that most transcription factors, including major functional transcription factors, are the same in different species although the binding site positions in the promoter are different. These results indicated that the signaling pathways involved in FGF21 gene transcription regulation are conservative in mammals. Truncated fragments recombinant vectors and luciferase reporter assay determined that camel FGF21 core promoter is located within the 800 bp region upstream of the TSS and an enhancer may exist between the -1000 and -2000 bp region. Combining molecular docking and in silico ADMET druggability prediction, two compounds were screened as the most promising candidate drugs specifically targeting FGF21. This study expanded the functions of these small molecules and provided a foundation for drug development targeting FGF21.

摘要

成纤维细胞生长因子21(FGF21)基因在葡萄糖和脂质代谢机制中起重要作用,是代谢性疾病颇具前景的治疗靶点。骆驼表现出独特的葡萄糖和脂质代谢调节特征,使其具备适应干旱和长期饥饿并生存的能力。然而,关于骆驼FGF21基因调控及其与人和小鼠之间差异的了解仍然有限。在本研究中,获得了骆驼FGF21基因转录起始位点(TSS)上游约2000 bp的启动子。生物信息学分析表明,人和骆驼TSS附近的近端启动子区域序列具有高度相似性。两个潜在的核心活性区域位于-445-612 bp区域。此外,骆驼FGF21启动子包含三个CpG岛(CGI),位于-435~-1168 bp区域,明显多于人和小鼠且更长。转录因子结合预测表明,尽管不同物种启动子中的结合位点位置不同,但包括主要功能转录因子在内的大多数转录因子是相同的。这些结果表明,FGF21基因转录调控所涉及的信号通路在哺乳动物中是保守的。截短片段重组载体和荧光素酶报告基因测定确定骆驼FGF21核心启动子位于TSS上游800 bp区域内,并且在-1000和-2000 bp区域之间可能存在增强子。结合分子对接和计算机辅助ADMET成药性预测,筛选出两种化合物作为最有前景的特异性靶向FGF21的候选药物。本研究扩展了这些小分子的功能,为靶向FGF21的药物开发提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09e3/10383868/d20410f32e5e/vetsci-10-00452-g001.jpg

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