Bioinformatic Analysis of the Genetic Basis of Differential Adeno-Associated Virus Production Capability of 293 Variants.

293个腺相关病毒变异株差异产生能力的遗传基础的生物信息学分析

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作者:Herzog Christopher R, Zhang Junping, Feng Xiaomin, Dang Thao Thi, Yu Xiangping, Huang Jie, Fang Fang, Gao Hongyu, Yu Xuhong, Wang Yue, Han Renzhi, Liu Yulong, Cornetta Kenneth, Xiao Weidong, Xu Weihong
Human embryonic kidney 293 (HEK 293) cells are the main producer cell line for recombinant adeno-associated virus (rAAV) production. However, AAV vector yields among 293 clones vary considerably. To elucidate the biological basis for these differences, whole genomes of an adherent and a suspension 293 cell clone with high-yield rAAV were sequenced using nanopore technology. All 293 cell derivative lines showed a twofold copy number gain at the adenoviral integration site across, suggesting a genome duplication event. To our surprise, the two high-producer clones, despite having been separately developed, are biologically closely grouped together as compared to other commonly used 293 clones. Their genomes contain a similar adenoviral gene integration region, which likely leads to high expression of proteins that facilitate AAV replication and packaging. Thus, genome duplication in the adenovirus integration locus may be a key factor affecting AAV production yield.

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