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环状RNA mmu-circ-Pax3.1表达载体的构建及初步验证

曹洋 尤双 姚洋 李村院 陈创夫 倪伟 胡圣伟

中国畜牧兽医2017,Vol.45Issue(10):2865-2870,6.
中国畜牧兽医2017,Vol.45Issue(10):2865-2870,6.DOI:10.16431/j.cnki.1671-7236.2017.10.006

环状RNA mmu-circ-Pax3.1表达载体的构建及初步验证

Construction and Preliminary Verification of Expression Vector of Circular RNA mmu-circ-Pax3.1

曹洋 1尤双 1姚洋 1李村院 1陈创夫 2倪伟 1胡圣伟1

作者信息

  • 1. 石河子大学生命科学学院,石河子832003
  • 2. 石河子大学动物科技学院,石河子832003
  • 折叠

摘要

Abstract

This study was aimed to investigate the feasibility of expressing mmu-circ-Pax3.1 by circular RNA expressed vector in vitro.The exists of mmu-circ-Pax3.1 was confirmed by reverse PCR and sequenced,and constructed pcDNA3.1(+) CircRNA-mmu-Pax3.1 through cloning the corresponding linear sequence into pcDNA3.1(+) CircRNA Mini Vector.The recombinant vector was identified by PCR,enzyme digestion and sequencing methods.The recombinant plasmid was transfected into 293 cells by Lipofectamine 2000 transfection reagent,transfected cells were observed under the inverted fluorescence microscope.Finally,the expression of mmu-circ-Pax3.1 was detected by RT-PCR in normal cells group,empty vector group and experimental group.The mmu-circ-Pax3.1 expression vector was successfully constructed,and the vector could make mmu-circ-Pax3.1 efficient transcription into 293 cells.The circular RNA expression vector constructed in this experiment by genetic engineering technology was transfected into 293 cells by liposome method,and transcribed mmu-circ-Pax3.1 efficiently and laid a foundation for further study for the function of mmu circ-Pax3.1.

关键词

环状RNA/载体构建/293细胞/转染

Key words

circular RNA/vector construction/293 cells/transfection

分类

生物科学

引用本文复制引用

曹洋,尤双,姚洋,李村院,陈创夫,倪伟,胡圣伟..环状RNA mmu-circ-Pax3.1表达载体的构建及初步验证[J].中国畜牧兽医,2017,45(10):2865-2870,6.

基金项目

国家自然基金项目“绵羊胚胎骨骼肌发育相关环状RNA的筛选和功能研究”(31660644) (31660644)

中国畜牧兽医

OA北大核心CSTPCD

1671-7236

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