Generation of a novel HEK293 luciferase reporter cell line by CRISPR/Cas9-mediated site-specific integration in the genome to explore the transcriptional regulation of the PGRN gene. Issue 1 (1st January 2019)

• Record Type: Journal Article
• Authors: Li, Yanqing; Li, Sai; Li, Yan; Xia, Haibin; Mao, Qinwen
• Is Part Of: Bioengineered. Volume 10:Issue 1(2019)
• Page Start: 98
• Page End: 107
• Publication Date: 2019-01-01
• Subjects: CRISPR/Cas9 -- PGRN -- knock-in -- luciferase -- transcriptional regulation -- HEK293; Biomedical engineering -- Periodicals; Biotechnology -- Periodicals; Microbiology -- Periodicals; 660.6
• DOI: 10.1080/21655979.2019.1607126
• Languages: English
• ISSNs: 2165-5987

Abstract

ABSTRACT: Progranulin has multiple functions in several physiological and pathological processes, including embryonic development, wound repair, tumorigenesis, inflammation and neurodegeneration. To investigate the transcriptional regulation of the PGRN gene, a luciferase knock-in reporter system was established in HEK293 cells by integrating luciferase gene in the genome controlled by the endogenous PGRN promoter using CRISPR/Cas9. PCR results demonstrated the site-specific integration of the exogenous luciferase gene into the genome. To validate the novel luciferase knock-in system, a CRISPR/Cas9 transcription activation/repression system for the PGRN gene was constructed and applied to the knock-in system. In addition, phorbol ester (phorbol 12-myristate, 13-acetate), previously reported as activating the expression of PGRN, was applied to the system. The results indicated that luciferase activity was directly correlated with the activity of the PGRN endogenous promoter. This novel system will be a useful tool for investigating the transcriptional regulation of PGRN, and it has great potential in screening the drugs targeting PGRN.