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Journal article

The genomic sequence of the Chinese hamster ovary (CHO)-K1 cell line

From

BGI Group1

GT Life Sciences2

Shenzhen Hospital3

University of Delaware4

Center for Microbial Biotechnology, Department of Systems Biology, Technical University of Denmark5

Department of Systems Biology, Technical University of Denmark6

Stanford University7

Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark8

Network Reconstruction in Silico Biology, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark9

Chinese hamster ovary (CHO)-derived cell lines are the preferred host cells for the production of therapeutic proteins. Here we present a draft genomic sequence of the CHO-K1 ancestral cell line. The assembly comprises 2.45 Gb of genomic sequence, with 24,383 predicted genes. We associate most of the assembled scaffolds with 21 chromosomes isolated by microfluidics to identify chromosomal locations of genes.

Furthermore, we investigate genes involved in glycosylation, which affect therapeutic protein quality, and viral susceptibility genes, which are relevant to cell engineering and regulatory concerns. Homologs of most human glycosylation-associated genes are present in the CHO-K1 genome, although 141 of these homologs are not expressed under exponential growth conditions.

Many important viral entry genes are also present in the genome but not expressed, which may explain the unusual viral resistance property of CHO cell lines. We discuss how the availability of this genome sequence may facilitate genome-scale science for the optimization of biopharmaceutical protein production.

Language: English
Publisher: Nature Publishing Group
Year: 2011
Pages: 735-741
Journal subtitle: Science and Business of Biotechnology
ISSN: 15461696 and 10870156
Types: Journal article
DOI: 10.1038/nbt.1932
ORCIDs: Andersen, Mikael Rørdam and Palsson, Bernhard

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