Literature DB >> 19002809

Evaluation of stable and highly productive gene amplified CHO cell line based on the location of amplified genes.

T Yoshikawa1, F Nakanishi, S Itami, D Kameoka, T Omasa, Y Katakura, M Kishimoto, K Suga.   

Abstract

In order to establish an easy and quick construction method for obtaining a stable and highly productive gene-amplified recombinant Chinese Hamster Ovary (CHO) cell line, variouskinds of stepwise methotrexate (MTX) selection were carriedout. The specific growth and production rates of the cell were compared with each other, and the distribution of the amplified gene location was determined using fluorescence in situ hybridization (FISH). The specific growth andproduction rates of the cell pool reached the highest levels under the selection condition in which the stepwise increase in the MTX concentration was most gradual; about 82% of amplified genes were observed near the telomeric region. During long-term cultivation without MTX, the percentage ofamplified genes near the telomeric region hardly changed, butthat of amplified genes at other regions decreased. Based on these results, stable and highly productive cell pools could be easily and quickly constructed and amplified and gradual stepwise increase of the MTX concentration. In addition, the FISH technique was powerful tool to evaluate highly productiveand stable gene-amplified cells based on the chromosomal location of the amplified gene.

Entities:  

Year:  2000        PMID: 19002809      PMCID: PMC3466717          DOI: 10.1023/A:1008111328771

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  36 in total

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  7 in total

1.  Assessment of UCOE on Recombinant EPO Production and Expression Stability in Amplified Chinese Hamster Ovary Cells.

Authors:  Zeynep Betts; Alan J Dickson
Journal:  Mol Biotechnol       Date:  2015-09       Impact factor: 2.695

2.  Genome sequence comparison between Chinese hamster ovary (CHO) DG44 cells and mouse using end sequences of CHO BAC clones based on BAC-FISH results.

Authors:  Shuichi Kimura; Takeshi Omasa
Journal:  Cytotechnology       Date:  2018-07-09       Impact factor: 2.058

3.  Identification of regulatory motifs in the CHO genome for stable monoclonal antibody production.

Authors:  Yasuhiro Takagi; Tomomi Yamazaki; Kenji Masuda; Shigeaki Nishii; Bunsei Kawakami; Takeshi Omasa
Journal:  Cytotechnology       Date:  2016-08-20       Impact factor: 2.058

4.  Identification of transgene integration loci of different highly expressing recombinant CHO cell lines by FISH.

Authors:  Christine Lattenmayer; Martina Loeschel; Willibald Steinfellner; Evelyn Trummer; Dethardt Mueller; Kornelia Schriebl; Karola Vorauer-Uhl; Hermann Katinger; Renate Kunert
Journal:  Cytotechnology       Date:  2006-11-15       Impact factor: 2.058

5.  Chromosome identification and its application in Chinese hamster ovary cells.

Authors:  Yihua Cao; Shuichi Kimura; Joon-Young Park; Miyuki Yamatani; Kohsuke Honda; Hisao Ohtake; Takeshi Omasa
Journal:  BMC Proc       Date:  2011-11-22

6.  Engineering a stable CHO cell line for the expression of a MERS-coronavirus vaccine antigen.

Authors:  Mun Peak Nyon; Lanying Du; Chien-Te Kent Tseng; Christopher A Seid; Jeroen Pollet; Kevin S Naceanceno; Anurodh Agrawal; Abdullah Algaissi; Bi-Hung Peng; Wanbo Tai; Shibo Jiang; Maria Elena Bottazzi; Ulrich Strych; Peter J Hotez
Journal:  Vaccine       Date:  2018-02-26       Impact factor: 3.641

7.  FISH-Based Analysis of Clonally Derived CHO Cell Populations Reveals High Probability for Transgene Integration in a Terminal Region of Chromosome 1 (1q13).

Authors:  Shengwei Li; Xiaoping Gao; Rui Peng; Sheng Zhang; Wei Fu; Fangdong Zou
Journal:  PLoS One       Date:  2016-09-29       Impact factor: 3.240

  7 in total

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