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作 者:龙熙[1] 袁晓 陈力 吴平先 张亮[1] 潘红梅[1] 郭宗义[1] 柴捷[1] LONG Xi;YUAN Xiao;CHEN Li;WU Pingxian;ZHANG Liang;PAN Hongmei;GUO Zongyi;CHAI Jie(Chongqing Academy of Animal Science,Key Laboratory of Pig Industry Sciences(Ministry of Agriculture),Chongqing 402460,China)
机构地区:[1]重庆市畜牧科学院,农业部养猪科学重点实验室,重庆402460
出 处:《华北农学报》2023年第S01期400-407,共8页Acta Agriculturae Boreali-Sinica
基 金:重庆市科研院所绩效激励引导专项(21530);国家重点研发计划项目(2021YFD1301105)。
摘 要:旨在初步分析猪CRYBB2的启动子活性以及转录调控元件。利用生物信息学分析、PCR扩增、基因克隆、细胞转染、双荧光素酶活性分析等方法,获得了CRYBB2启动子区域的序列特征,构建了不同片段长度的CRYBB2启动子区的双荧光素酶报告基因载体并分析了其荧光素酶活性,进而确定了CRYBB2的核心启动子区域以及关键的调控区域,最后还预测了关键调控区域的转录因子及其结合位点。结果表明,CRYBB2候选启动子区可能包含4个核心启动子以及1个CpG岛,-52~-3 bp可能为CRYBB2基因的核心启动子区域,-505~-19 bp为CRYBB2基因启动子的关键调控区域,且发挥正向调节作用,而-2060~-505 bp不存在任何对CRYBB2基因启动子活性有影响的调控元件;CRYBB2启动子的关键调控区域包含多个潜在的转录因子结合位点,如TBP、NFIA、FOXP1、NKX2-8、KLF4、Tcf3、Crx、SNAI3、Rfx1和CREB1等。为进一步研究猪CRYBB2的表达机制奠定了基础。The purpose of this study was to preliminarily analyze the promoter activity and transcription regulatory elements of porcine CRYBB2.Using bioinformatics analysis,PCR amplification,gene cloning,cell transfection,double luciferase activity analysis and other methods,we obtained the sequence characteristics of CRYBB2 promoter region,constructed double luciferase reporter gene vectors of CRYBB2 promoter region with different fragment lengths,analyzed its luciferase activity,and then determined the core promoter region and key regulatory region of CRYBB2.Finally,the transcription factors and their binding sites in key regulatory regions were predicted.The results showed that the candidate promoter region of CRYBB2 might contain four core promoters and one CpG island.-52--3 bp might be the core promoter region of CRYBB2 gene,and-505--19 bp might be the key regulatory region of CRYBB2 gene promoter,which played a positive regulatory role,while-2060--505 bp didn′t have any regulatory elements that affected the activity of CRYBB2 gene promoter.The key regulatory region of CRYBB2 promoter contained multiple potential transcription factor binding sites,such as TBP,NFIA,FOXP1,NKX2-8,KLF4,Tcf3,Crx,SNAI3,Rfx1 and CREB1.This study laid a foundation for further study on the expression mechanism of porcine CRYBB2.
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