| Literature DB >> 23873082 |
Nathan E Lewis1, Xin Liu, Yuxiang Li, Harish Nagarajan, George Yerganian, Edward O'Brien, Aarash Bordbar, Anne M Roth, Jeffrey Rosenbloom, Chao Bian, Min Xie, Wenbin Chen, Ning Li, Deniz Baycin-Hizal, Haythem Latif, Jochen Forster, Michael J Betenbaugh, Iman Famili, Xun Xu, Jun Wang, Bernhard O Palsson.
Abstract
Chinese hamster ovary (CHO) cells, first isolated in 1957, are the preferred production host for many therapeutic proteins. Although genetic heterogeneity among CHO cell lines has been well documented, a systematic, nucleotide-resolution characterization of their genotypic differences has been stymied by the lack of a unifying genomic resource for CHO cells. Here we report a 2.4-Gb draft genome sequence of a female Chinese hamster, Cricetulus griseus, harboring 24,044 genes. We also resequenced and analyzed the genomes of six CHO cell lines from the CHO-K1, DG44 and CHO-S lineages. This analysis identified hamster genes missing in different CHO cell lines, and detected >3.7 million single-nucleotide polymorphisms (SNPs), 551,240 indels and 7,063 copy number variations. Many mutations are located in genes with functions relevant to bioprocessing, such as apoptosis. The details of this genetic diversity highlight the value of the hamster genome as the reference upon which CHO cells can be studied and engineered for protein production.Entities:
Mesh：
Year: 2013 PMID： 23873082 DOI： 10.1038/nbt.2624
Source DB: PubMed Journal: Nat Biotechnol ISSN： 1087-0156 Impact factor: 54.908