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猪CRYBB2基因启动子的克隆、活性及转录调控元件分析

龙熙 袁晓 陈力 吴平先 张亮 潘红梅 郭宗义 柴捷

华北农学报2023,Vol.38Issue(z1):400-407,8.
华北农学报2023,Vol.38Issue(z1):400-407,8.DOI:10.7668/hbnxb.20193874

猪CRYBB2基因启动子的克隆、活性及转录调控元件分析

Cloning,Transcriptional Activity and Regulatory Elements Analysis of Porcine CRYBB2 Gene Promoter

龙熙 1袁晓 1陈力 1吴平先 1张亮 1潘红梅 1郭宗义 1柴捷1

作者信息

  • 1. 重庆市畜牧科学院,农业部养猪科学重点实验室,重庆 402460
  • 折叠

摘要

Abstract

The purpose of this study was to preliminarily analyze the promoter activity and transcription regula-tory 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-2 060—-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.

关键词

/CRYBB2/启动子/转录活性/转录因子

Key words

Pig/CRYBB2/Promoter/Transcriptional activity/Transcription factor

分类

农业科技

引用本文复制引用

龙熙,袁晓,陈力,吴平先,张亮,潘红梅,郭宗义,柴捷..猪CRYBB2基因启动子的克隆、活性及转录调控元件分析[J].华北农学报,2023,38(z1):400-407,8.

基金项目

重庆市科研院所绩效激励引导专项(21530) (21530)

国家重点研发计划项目(2021YFD1301105) (2021YFD1301105)

华北农学报

OA北大核心CSCDCSTPCD

1000-7091

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