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Identification of regulatory motifs in the CHO genome for stable monoclonal antibody production.
Takagi, Yasuhiro; Yamazaki, Tomomi; Masuda, Kenji; Nishii, Shigeaki; Kawakami, Bunsei; Omasa, Takeshi.
Afiliação
  • Takagi Y; Institute of Bioscience and Bioindustry, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima, 770-8506, Japan.
  • Yamazaki T; Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka, 565-0871, Japan.
  • Masuda K; Biotechnology Laboratories, Astellas Pharma Inc., 5-2-3 Tokodai, Tsukuba-shi, Ibaraki, 300-2698, Japan.
  • Nishii S; TOYOBO Co.Ltd., 10-24 Toyo-cho, Tsuruga, Fukui, 914-8550, Japan.
  • Kawakami B; TOYOBO Co.Ltd., 10-24 Toyo-cho, Tsuruga, Fukui, 914-8550, Japan.
  • Omasa T; TOYOBO Co.Ltd., 10-24 Toyo-cho, Tsuruga, Fukui, 914-8550, Japan.
Cytotechnology ; 69(3): 451-460, 2017 Jun.
Article em En | MEDLINE | ID: mdl-27544513
ABSTRACT
Chinese hamster ovary (CHO) cell lines are widely used for therapeutic protein production. When a transgene is integrated into the genome of a CHO cell, the expression level is highly dependent on the site of integration because of positional effects such as gene silencing. To overcome negative positional effects and establish stable CHO cell lines with high productivity, several regulatory DNA elements are used in vector construction. Previously, we established the CHO DR1000L-4N cell line, a stable and high copy number Dhfr gene-amplified cell line. It was hypothesized that the chromosomal location of the exogenous gene-amplified region in the CHO DR1000L-4N genome contains regulatory motifs for stable protein production. Therefore, we isolated DNA regulatory motifs from the CHO DR1000L-4N cell line and determined whether these motifs act as an insulator. Our results suggest that stable expression of a transgene can be promoted by the CHO genome sequence, and it would be a powerful tool for therapeutic protein manufacturing.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article