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2025年8月8日 星期五
农业生物技术学报  2024, Vol. 32 Issue (3): 578-586    DOI: 10.3969/j.issn.1674-7968.2024.03.008
  研究论文与报告 本期目录 | 过刊浏览 | 高级检索 |
奶山羊转录因子FoxO1启动子克隆及活性分析
赫秋亚, 罗军*, 高梁嘉慧, 邬娇, 姚玮玮
西北农林科技大学 动物科技学院/陕西省农业分子生物学重点实验室,杨凌 712100
Cloning and Activity Analysis of Transcription Factor FoxO1 Promoter in Dairy Goat (Capra hircus)
HE Qiu-Ya, LUO Jun*, GAO Liang-Jia-Hui, WU Jiao, YAO Wei-Wei
College of Animal Science and Technology/Shaanxi Provincial Key Laboratory of Molecular Biology for Agriculture, Northwest A& F University, Yangling 712100, China
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摘要 叉头框蛋白O1 (forkhead box protein O1, FoxO1)是调控脂肪酸代谢的关键转录因子。尽管在非反刍动物中已经证明FoxO1启动子受上游转录因子的调节,但FoxO1启动子在奶山羊(Capra hircus)泌乳过程中的调控机制尚不清楚。本研究根据云南黑山羊基因组序列设计引物,克隆FoxO1基因5'侧翼序列;利用在线软件对FoxO1启动子序列进行生物信息学分析,预测转录因子的结合位点;利用缺失突变方法构建包含不同长度FoxO1启动子片段的双荧光素酶报告载体,利用重叠延伸PCR方法构建包含顺式作用元件突变的双荧光素酶报告载体,与内参载体共转染山羊乳腺上皮细胞(goat mammary epithelial cell, GMEC),利用双荧光素酶系统检测启动子活性。结果显示,从奶山羊血液基因组中克隆得到1 500 bp FoxO1启动子序列;生物信息学分析发现,FoxO1启动子上存在2个FoxO1结合位点;缺失突变结果表明,FoxO1启动子的活性中心位于转录起始位点上游-95~-24 bp;过表达FoxO1可显著上调FoxO1启动子活性;突变近侧的FKH1 (forkhead transcription factor 1)结合位点(-359 bp),FoxO1启动子活性显著下降,同时突变FKH1和FKH2位点后,FoxO1启动子活性与FKH1位点单突变无显著变化。上述结果表明,FoxO1通过与启动子上FKH结合元件的顺式作用促进FoxO1转录。本研究为FoxO1基因启动子的功能研究提供理论参考,为构建奶山羊乳腺组织中脂肪酸代谢网络提供基础资料。
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赫秋亚
罗军
高梁嘉慧
邬娇
姚玮玮
关键词 叉头框蛋白O1 (FoxO1)启动子转录调控脂肪酸代谢山羊乳腺上皮细胞(GMEC)    
Abstract:Forkhead box protein O1 (FoxO1) is a key transcription factor regulating fatty acid metabolism. Although FoxO1 promoter has been shown to be regulated by upstream transcription factors in non-ruminants, the mechanism of FoxO1 regulation during lactation in dairy goats (Capra hircus) remains unclear. This study designed primers based on the genome sequence of Yunnan black goat and cloned the 5' flanking sequence of FoxO1 gene. Bioinformatic analysis of FoxO1 promoter sequence was performed using online software to predict the binding sites of transcription factors. Double luciferase reporter vectors containing different lengths of FoxO1 promoter fragments were constructed by deletion mutation method, and double luciferase reporter vectors containing mutations of cis-acting elements were constructed by overlapping extension PCR method. The recombinant constructs and reference vectors were co-transfected into goat mammary epithelial cells (GMEC), and the promoter activity was detected by dual luciferase system. The results showed that 1 500 bp FoxO1 promoter sequence was cloned from the blood genome of dairy goats. Bioinformatics analysis revealed 2 binding sites of FoxO1 on the FoxO1 promoter. Deletion mutation results showed that region from -95 to -24 bp was necessary for basal transcription activity of FoxO1 promoter. Overexpression of FoxO1 significantly increased the activity of FoxO1 promoter. Mutation of the forkhead transcription factor 1 (FKH1) (-359 bp) site showed a significant decrease in FoxO1 promoter activity compared to wild type, but unchanged after mutation of FKH1 and FKH2 sites. Above results suggest that FoxO1 might promote FoxO1 transcription by binding to the FKH elements located at the promoter. This study provides theoretical reference for the functional study of the FoxO1 gene promoter and basic data for constructing the fatty acid metabolism network in mammary gland of dairy goats.
Key wordsForkhead box protein O1 (FoxO1)    Promoter    Transcriptional regulation    Fatty acid metabolism    Goat mammary epithelial cell (GMEC)
收稿日期: 2023-03-28     
ZTFLH:  S826.9+4  
基金资助:国家自然科学基金(31772575; 32202643)
通讯作者: *luojun@nwsuaf.edu.cn   
引用本文:   
赫秋亚, 罗军, 高梁嘉慧, 邬娇, 姚玮玮. 奶山羊转录因子FoxO1启动子克隆及活性分析[J]. 农业生物技术学报, 2024, 32(3): 578-586.
HE Qiu-Ya, LUO Jun, GAO Liang-Jia-Hui, WU Jiao, YAO Wei-Wei. Cloning and Activity Analysis of Transcription Factor FoxO1 Promoter in Dairy Goat (Capra hircus). 农业生物技术学报, 2024, 32(3): 578-586.
链接本文:  
https://journal05.magtech.org.cn/Jwk_ny/CN/10.3969/j.issn.1674-7968.2024.03.008     或     https://journal05.magtech.org.cn/Jwk_ny/CN/Y2024/V32/I3/578
 
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