ADRB2 Gene Knockout in Human Primary T Cells by Multiple sgRNAs Construced using CRISPR/Cas9 Technology.
10.19746/j.cnki.issn.1009-2137.2019.05.050
- Author:
Yu SUN
1
;
Dan LIU
1
;
Ming SHI
2
;
Jun-Nian ZHENG
3
Author Information
1. Jiangsu Provincial Institute of Cancer Biotherapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
2. Jiangsu Provincial Institute of Cancer Biotherapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China,E-mail: shiming_amms@sina.cn.
3. Jiangsu Provincial Institute of Cancer Biotherapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China,E-mail: jnzheng@xzhmu.edu.cn.
- Publication Type:Journal Article
- MeSH:
CRISPR-Cas Systems;
Gene Editing;
Gene Knockout Techniques;
Humans;
RNA, Guide;
Receptors, Adrenergic, beta-2;
genetics;
T-Lymphocytes
- From:
Journal of Experimental Hematology
2019;27(5):1682-1690
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To knockout ADRB2 gene rapidly and efficiently in human primary T cells by using CRISPR/Cas9 technology and multiple sgRNAs strategy.
METHODS:Six paired-sgRNAs, which were designed to target the 5' constitutive coding exons of ADRB2 gene, were cloned into pGL3-U6-sgRNA-PGK-Puro vector separately. The expre-ssion vectors containing the single sgRNAs were constructed and transiently co-transfected into HEK-293T cell line with Cas9 expression vector. The sgRNA-mediated cleavage efficiency was tested by T7EN I digestion assay. Concatenating four highly efficient paired sgRNAs were cloned into pGL3-U6-sgRNA-ccdB-EF1α-Puro expression vector. The reco-mbinant plasmid allows the cells to express 4 sgRNAs, which target different sites on the ADRB2 genomic locus. The cleavage efficiency and mutation model were tested by T7EN I digest assay and T-A cloning technique. Multiple sgRNAs plasmid and Cas9 plasmid was transiently transferred into human primary T cells by electroporation. Flow cytometry (FCM) was used to detect the knockout efficiency of β2 adrenergic receptor (β2-AR).
RESULTS:The results of T7EN I digestion and TA cloning sequencing showed that the multiple sgRNAs strategy could obtain more abundant mutation types and higher gene editing efficiency than single sgRNA. In addition to the deletion and insertion of bases, large fragment DNA deletions and inversions could be observed. All of the random 10 TA clones for detection were genetically modified, thus the mutation efficiency was as high as 100%. FCM assay showed that 43.09% of the cells in the control T cells were β2-AR positive, but the proportion of β2-AR positive cells in the multiple sgRNAs electrotransformed T cells decreased to 25.61%.
CONCLUSION:A method, which is simple and operable, for knocking out β2-AR in human primary T cells has been established preliminarily. The results are helpful for the further study of the role of β2-AR in human T cells.
