Engineering of HEK293T Cell Factory for Lentiviral Production by High-Throughput Selected Genes

被引:0
|
作者
Zhang, Xinyue [1 ,2 ]
Li, Siwei [2 ]
Wang, Yujie [2 ,3 ]
Dai, Yingcai [2 ,4 ]
Bi, Changhao [1 ,2 ]
Zhang, Xueli [1 ,2 ]
机构
[1] Tianjin Univ Sci & Technol, Tianjin 300308, Peoples R China
[2] Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Tianjin, Peoples R China
[3] Binzhou Med Univ, Binzhou, Shandong, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai, Peoples R China
来源
CRISPR JOURNAL | 2024年 / 7卷 / 05期
基金
中国国家自然科学基金;
关键词
VECTOR; TRANSCRIPTION; INHIBITION; ENHANCER; RNA;
D O I
10.1089/crispr.2024.0016
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lentiviral vectors (LVs) are crucial tools in gene therapy and bioproduction, but high-yield LV production systems are urgently needed. Using clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 high-throughput screening, we identified nine critical genes (LDAH, GBP3, BPIFC, NHLRC1, NHLRC3, ZNF425, TTC37, LRRC4B, and SPINK6) from 17,501 genes that limit LV packaging and formation. Knocking out these genes in HEK293T cells significantly increased virus production, with LDAH knockout exhibiting a 6.63-fold increase. Studies on multigene knockouts demonstrated that the cumulative effects of different gene knockouts can significantly enhance lentivirus production in HEK293T cells. Triple knockout of GBP3, BPIFC, and LDAH increased LV titer by similar to 8.33-fold, and knockout (or knockdown) of GBP3, NHLRC1, and NHLRC3 increased LV titer by similar to 6.53-fold. This study established HEK293T cell lines with multiple genes knockout for efficient LV production, providing reliable technical support for LV production and application and offering new perspectives for studying LV packaging mechanisms and related virus research.
引用
收藏
页码:272 / 282
页数:11
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