Evidence map›Paper›PMID 29703950›Full record

ArticleScientific reports2018

Human rhinovirus internal ribosome entry site element enhances transgene expression in transfected CHO-S cells.

Yu-Rong Chai, Meng-Meng Ge, Ting-Ting Wei, Yan-Long Jia, Xiao Guo, Tian-Yun Wang

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Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yu-Rong ChaiDepartment of Histology and Embryology, School of Basic Medical Sciences, University of Zhengzhou, 450001, Henan, China.ORCID 0000-0002-9213-5302
Meng-Meng GeDepartment of Histology and Embryology, School of Basic Medical Sciences, University of Zhengzhou, 450001, Henan, China.
Ting-Ting WeiDepartment of Histology and Embryology, School of Basic Medical Sciences, University of Zhengzhou, 450001, Henan, China.
Yan-Long JiaInternational Joint Research Laboratory for Recombiant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Xiao GuoDepartment of Biochemistry and Molecular Biology, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Tian-Yun WangDepartment of Biochemistry and Molecular Biology, Xinxiang Medical University, Xinxiang, 453003, Henan, China. wtianyuncn@126.com.ORCID 0000-0002-0793-1006

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chinese hamster ovary (CHO) cells are mainly used for recombinant protein production. However, the unstable transgene expression and lower transgene copy numbers are the major issues need to be resolved. Here, eleven internal ribosome entry site (IRES) elements from viral and cellular IRES were evaluated for foreign gene expression in CHO-S cells. We constructed eleven fusing plasmids containing different IRES sequences downstream of the enhanced green fluorescent protein (EGFP) gene. EGFP expression was detected by flow cytometry and the transgene copy number was evaluated by quantitative PCR. The erythropoietin (EPO) protein was also used to assess the stronger IRES. The results showed that IRES from human rhinovirus (HRV) exhibited the highest EGFP expression level under transient and stable transfections. The EGFP expression level of vector with IRES from HRV was related to the gene copy number in stably transfected CHO-S cells. Moreover, IRES from HRV induced higher expression level of EPO compared with one mutant IRES from EMCV in transfected cells. In conclusion, IRES from HRV can function as a strong IRES element for stable expression in CHO-S cells, which could potentially guide more effective foreign gene expression in CHO-S cells.

Indexed as

Gene ExpressionGenetic VectorsInternal Ribosome Entry SitesAnimalsCHO CellsCricetulusErythropoietinGene DosageGenes, ReporterGenomic InstabilityGreen Fluorescent ProteinsHumansRecombinant ProteinsRhinovirusenhanced green fluorescent proteinErythropoietinGreen Fluorescent ProteinsInternal Ribosome Entry SitesRecombinant Proteins

Identifiers

PMID29703950
PMCPMC5923211

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