Microarray and proteomics expression profiling identifies several candidates, including the valosin-containing protein (VCP), involved in regulating high cellular growth rate in production CHO cell lines
Abstract
A high rate of cell growth (µ) leading to rapid accumulation of viable biomass is a desirable phenotype during scale up operations and the early stages of production cultures. In order to identify genes and proteins that contribute to higher growth rates in Chinese hamster ovary (CHO) cells, a combined approach using microarray and proteomic expression profiling analysis was carried out on two matched pairs of CHO production cell lines that displayed either fast or slow growth rates. Statistical analysis of the microarray and proteomic data separately resulted in the identification of 118 gene transcripts and 58 proteins that were differentially expressed between the fast‐ and slow‐growing cells. Overlap comparison of both datasets identified a priority list of 21 candidates associated with a high growth rate phenotype in CHO. Functional analysis (by siRNA) of five of these candidates identified the valosin‐containing protein (VCP) as having a substantial impact on CHO cell growth and viability. Knockdown of HSPB1 and ENO1 also had an effect on cell growth (negative and positive, respectively). Further functional validation in CHO using both gene knockdown (siRNA) and overexpression (cDNA) confirmed that altered VCP expression impacted CHO cell proliferation, indicating that VCP and other genes and proteins identified here may play an important role in the regulation of CHO cell growth during log phase culture and are potential candidates for CHO cell line engineering strategies. Biotechnol. Bioeng. 2010; 106: 42–56. © 2010 Wiley Periodicals, Inc.
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Comparison of proteomic profiles of fast vs slow growing CHO clones has already identified the valosin-containing protein (VCP) as a potential candidate for enhancement of cell growth by cell engineering.
“Indeed, comparison of proteomic profiles of fast vs slow growing CHO clones has already identified the valosin-containing protein (VCP) as a potential candidate for enhancement of cell growth by cell engineering (Doolan et al., 2010).”
From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Doolan et al., 2010
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Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625 · see citing works
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Therapeutic glycoprotein production in mammalian cells
Lalonde, M.-E., & Durocher, Y. (2017) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2017.04.028 · Cited by 296 · see citing works
- Authors
- Doolan, P., Meleady, P., Barron, N., Henry, M., Gallagher, R., Gammell, P., Melville, M., Sinacore, M., McCarthy, K., Leonard, M., Charlebois, T., & Clynes, M.
- Affiliations
- Dublin City University (IE)
- Pfizer (Ireland) (IE)
- Pfizer (United States) (US)
- Biogen (United States) (US)
- Corresponding author
- Doolan, Padraig
- Venue
- Biotechnology and Bioengineering
- Publisher
- Wiley
- Published
- 2010-03-19
- Volume
- 106
- Issue
- 1
- Pages
- 42-56
- ISSN
- 0006-3592 (ISSN-L)
- 1097-0290
- OpenAlex
- W2146901740
- Cited by
- 84
- References
- 1
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 1 · 2019: 3 · 2018: 5 · 2017: 11 · 2015: 10 · 2014: 10 · 2013: 8 · 2012: 8
- FWCI
- 4.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biotechnology and Bioengineering (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
- Keywords
- VCP, HSPB1, alpha-enolase, differentially expressed genes, differentially expressed proteins, cell proliferation, cell viability, siRNA knockdown, cDNA overexpression, recombinant protein expression
- MeSH terms
- Valosin Containing Protein, Adenosine Triphosphatases, Animals, Cell Cycle, Cricetulus, Epithelial Cells, Cricetinae, Up-Regulation, Gene Expression, CHO Cells, Cell Cycle Proteins, Proteome, Gene Silencing, Gene Expression Profiling, RNA, Small Interfering
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