核转录因子激活蛋白-1对PPARδ表达的调控作用

目的研究在过氧化物酶体增长因子活化受体δ(PPARδ)表达中的相关调控因子。方法用RT-PCR扩增人类PPARδ启动子序列,通过Deletion及重组将不同长短的PPARδ启动子序列转化到PGL3-basic载体中,转染LOVO细胞,通过观测各重组体转染活性,确定PPARδ启动子活性区域。再通过电泳迁移率变更分析(EMSA)、突变等方法确定核转录因子激活蛋白-1(AP1)对PPARδ表达的作用。结果Deletion及重组转染后发现PPARδ启动子活性区域在序列3361~3464之间,EMSA、突变发现AP1因子结合位点突变后转染活性明显降低。结论AP1因子结合位点突变后转染活性明显降低,提示A...

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Published inXi'an jiao tong da xue xue bao. Journal of Xi'an Jiaotong University (medical sciences). Yi xue ban Vol. 26; no. 4; pp. 312 - 315
Main Author 蒋晓刚 毛泽斌 孟照俊 吕晓凤 俞小瑞
Format Journal Article
LanguageChinese
Published 西安交通大学环境与疾病相关基因教育部重点实验室,陕西西安,710061%北京大学医学部生化系,北京,853006 2005
西安交通大学医学院遗传与分子生物学系
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ISSN1671-8259
DOI10.3969/j.issn.1671-8259.2005.04.003

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Abstract 目的研究在过氧化物酶体增长因子活化受体δ(PPARδ)表达中的相关调控因子。方法用RT-PCR扩增人类PPARδ启动子序列,通过Deletion及重组将不同长短的PPARδ启动子序列转化到PGL3-basic载体中,转染LOVO细胞,通过观测各重组体转染活性,确定PPARδ启动子活性区域。再通过电泳迁移率变更分析(EMSA)、突变等方法确定核转录因子激活蛋白-1(AP1)对PPARδ表达的作用。结果Deletion及重组转染后发现PPARδ启动子活性区域在序列3361~3464之间,EMSA、突变发现AP1因子结合位点突变后转染活性明显降低。结论AP1因子结合位点突变后转染活性明显降低,提示AP1是PPARδ的一个增强子。
AbstractList 目的研究在过氧化物酶体增长因子活化受体δ(PPARδ)表达中的相关调控因子。方法用RT-PCR扩增人类PPARδ启动子序列,通过Deletion及重组将不同长短的PPARδ启动子序列转化到PGL3-basic载体中,转染LOVO细胞,通过观测各重组体转染活性,确定PPARδ启动子活性区域。再通过电泳迁移率变更分析(EMSA)、突变等方法确定核转录因子激活蛋白-1(AP1)对PPARδ表达的作用。结果Deletion及重组转染后发现PPARδ启动子活性区域在序列3361~3464之间,EMSA、突变发现AP1因子结合位点突变后转染活性明显降低。结论AP1因子结合位点突变后转染活性明显降低,提示AP1是PPARδ的一个增强子。
R392.11; 目的研究在过氧化物酶体增长因子活化受体δ(PPARδ)表达中的相关调控因子.方法用RT-PCR扩增人类PPARδ启动子序列,通过Deletion及重组将不同长短的PPARδ启动子序列转化到PGL3-basic载体中,转染LOVO细胞,通过观测各重组体转染活性,确定PPARδ启动子活性区域.再通过电泳迁移率变更分析(EMSA)、突变等方法确定核转录因子激活蛋白-1(AP1)对PPARδ表达的作用.结果 Deletion及重组转染后发现PPARδ启动子活性区域在序列3361~3464之间,EMSA、突变发现AP1因子结合位点突变后转染活性明显降低.结论 AP1因子结合位点突变后转染活性明显降低,提示AP1是PPARδ的一个增强子.
Author 蒋晓刚 毛泽斌 孟照俊 吕晓凤 俞小瑞
AuthorAffiliation 西安交通大学医学院遗传与分子生物学系 西安交通大学环境与疾病相关基因教育部重点实验室,陕西西安710061 北京大学医学部生化系,北京853006
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Author_FL Meng Zhaojun
Lü Xiaofeng
Yu Xiaorui
Jiang Xiaogang
Mao Zebin
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Keywords 突变
过氧化物酶体增长因子活化受体δ
转染
核转录因子激活蛋白-1
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SubjectTerms 核转录因子激活蛋白-1
突变
转染
过氧化物酶体增长因子活化受体δ
Title 核转录因子激活蛋白-1对PPARδ表达的调控作用
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