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PERV的整合对HEK293细胞中HERV-W mRNA表达的影响

马玲 唐海波 李军 白安斌 王志强 吴健敏

中国人兽共患病学报2017,Vol.33Issue(7):592-598,7.
中国人兽共患病学报2017,Vol.33Issue(7):592-598,7.DOI:10.3969/j.issn.1002-2694.2017.07.004

PERV的整合对HEK293细胞中HERV-W mRNA表达的影响

Effects of the integration of PERV on HERV-W mRNA expression in HEK293 cells

马玲 1唐海波 1李军 1白安斌 1王志强 2吴健敏3

作者信息

  • 1. 广西壮族自治区兽医研究所,广西兽医生物技术重点实验室,南宁530001
  • 2. 广西大学亚热带农业生物资源保护与利用国家重点实验室,南宁530004
  • 3. 广西大学生命科学与技术学院,南宁 530004
  • 折叠

摘要

Abstract

To find out whether the integration of PERV in HEK293 cells influence the expression profile of HERV-W,based on the gene sequences of H ERV-W in GenBank,the primers of H ERV-W gag,pol,env,env from locus 7q21.2 genes as well as humanβ-actin were synthesized respectively and were used to develop the means of SYBR Green I real-time reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to detect the mRNA expression of these genes in HEK293 cells and PERV-infected HEK293 cells.Experiments showed that these RT-qPCR methods were of good specificity,sensitivity and stability:the standard curves could ensure the correlation coefficients to be all above 0.99 and the amplification efficiency were between 95% and 110%,which verified that these methods could be used to detect the mRNA of HERV-W and humanβ-actin in culture cells.Through the detection and analysis of relative gene expression data using the 2-△△ct method,we found that the mRNA level of HERV-W gag,pol,env,env from locus 7q21.2 genes as well as humanβ-actin in PERV-infected HEK293 cells increased,after integration,by 37.08,42.56,2.49 and 13.17 times than in non-infected HEK293 cells,respectively.Results provide a reference to further evaluate the safety of PERV pathogen in xenotransplantation.

关键词

PERV/HERV-W/整合/表达/影响

Key words

PERV/HERV-W/integration/expression/influence

分类

医药卫生

引用本文复制引用

马玲,唐海波,李军,白安斌,王志强,吴健敏..PERV的整合对HEK293细胞中HERV-W mRNA表达的影响[J].中国人兽共患病学报,2017,33(7):592-598,7.

基金项目

Supported by the National Natural Science Foundation of China (No.31260613),the Natural Science Foundation of Guangxi Province (No.2015GXNSFAA139089),and the Guangxi Key Laboratory of Animal Vaccines and New Technology Open Fund (No.14-045-31-B-5)国家自然科学基金(No.31260613) (No.31260613)

广西自然科学基金(No.2015GXNSFAA139089)和广西畜禽疫苗新技术重点实验室开放基金项目(No.14-045-31-B-5)联合资助 (No.2015GXNSFAA139089)

中国人兽共患病学报

OA北大核心CSCDCSTPCD

1002-2694

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