Skip to main content
Log in

Alternative Promoters Regulate Cold Inducible RNA-Binding (CIRP) Gene Expression and Enhance Transgene Expression in Mammalian Cells

  • Published:
Molecular Biotechnology Aims and scope Submit manuscript

Abstract

The use of a temperature shift cultivation to enhance recombinant protein yield is widely utilised in the bioprocessing industry. The responses of mammalian cells to heat stress are well characterized; however, the equivalent cold stress responses are not. In particular, the transcriptional mechanisms that lead to enhanced gene-specific expression upon cold stress have yet to be elucidated. We report here in silico and experimental identification and characterization of transcriptional control elements that regulate cold inducible RNA-binding (CIRP) gene expression and demonstrate these can be used for enhanced transgene expression. In silico analysis identified the core CIRP promoter and a number of conserved transcription factor-binding sites across mammalian species. The core promoter was confirmed by experimental studies that located the basal transcriptional regulatory elements of CIRP within 264 nucleotides upstream of the transcription start site. Deletion analysis of a fragment from -264 to -64 that contained two putative CAAT-binding sites abolished promoter activity. A second promoter was identified in the region -452 to -264 of the transcription start site which was able to drive transcription independent of the core promoter. As the two CIRP promoters were transcriptionally active and possibly cold responsive, we used electrophoretic mobility shift assays to show that both promoter regions are able to bind factors within a nuclear extract in a dose-dependent manner and that the formation of these complexes was specific to the promoter regions. Finally, we successfully demonstrate using a reporter gene approach that enhanced transgene expression can be achieved using the identified CIRP promoter.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Al-Fageeh, M. B., & Smales, C. M. (2006). Control and regulation of the cellular responses to cold shock: The responses in yeast and mammalian systems. Biochemical Journal, 397, 247–259.

    Article  CAS  Google Scholar 

  2. Al-Fageeh, M. B., Marchant, R. J., Carden, M. J., & Smales, C. M. (2006). The cold-shock response in cultured mammalian cells: Harnessing the response for the improvement of recombinant protein production. Biotechnology and Bioengineering, 93, 829–835.

    Article  CAS  Google Scholar 

  3. Ermolenko, D. N., & Makhatadze, G. I. (2002). Bacterial cold-shock proteins. Cellular and Molecular Life Sciences, 59, 1902–1913.

    Article  CAS  Google Scholar 

  4. Roobol, A., Carden, M. J., Newsam, R. J., & Smales, C. M. (2009). Biochemical insights into the mechanisms central to the response of mammalian cells to cold-stress and subsequent rewarming. FEBS Journal, 276, 286–302.

    Article  CAS  Google Scholar 

  5. Roobol, A., Roobol, J., Carden, M. J., Bastide, A., Willis, A. E., Dunn, W., et al. (2011). Ataxia-telangiectasia mutated and Rad3-related kinase (ATR) is activated by mild hypothermia in mammalian cells and subsequently activates p53. Biochemical Journal, 435, 499–508.

    Article  CAS  Google Scholar 

  6. Marchant, R. J., Al-Fageeh, M. B., Underhill, M. F., Racher, A. J., & Smales, C. M. (2008). Metabolic rates, growth phase, and mRNA levels influence cell-specific antibody production levels from in vitro cultured mammalian cells at sub-physiological temperatures. Molecular Biotechnology, 39, 69–77.

    Article  CAS  Google Scholar 

  7. Underhill, M. F., Marchant, R. J., Carden, M. J., James, D. C., & Smales, C. M. (2006). On the effect of transient expression of mutated eIF2alpha and eIF4E eukaryotic translation initiation factors on reporter gene expression in mammalian cells upon cold-shock. Molecular Biotechnology, 34, 141–149.

    Article  CAS  Google Scholar 

  8. Masterton, R. J., Roobol, A., Al-Fageeh, M. B., Carden, M. J., & Smales, C. M. (2010). Post-translational events of a model reporter protein proceed with higher fidelity and accuracy upon mild hypothermic culturing of Chinese hamster ovary cells. Biotechnology and Bioengineering, 105, 215–220.

    Article  CAS  Google Scholar 

  9. Gammell, P., Barron, N., Kumar, N., & Clynes, M. (2007). Initial identification of low temperature and culture stage induction of miRNA expression in suspension CHO-K1 cells. Journal of Biotechnology, 130, 213–218.

    Article  CAS  Google Scholar 

  10. Beer, C., Buhr, P., Hahn, H., Laubner, D., & Wirth, M. (2003). Gene expression analysis of murine cells producing amphotropic mouse leukaemia virus at a cultivation temperature of 32 and 37 °C. Journal of General Virology, 84, 1677–1686.

    Article  CAS  Google Scholar 

  11. Underhill, M. F., & Smales, C. M. (2007). The cold-shock response in mammalian cells: Investigating the HeLa cell cold-shock proteome. Cytotechnology, 53, 47–53.

    Article  CAS  Google Scholar 

  12. Clarke, C., Doolan, P., Barron, N., Meleady, P., O’Sullivan, F., Gammell, P., et al. (2011). Large scale microarray profiling and coexpression network analysis of CHO cells identifies transcriptional modules associated with growth and productivity. Journal of Biotechnology, 155, 350–359.

    Article  CAS  Google Scholar 

  13. Bosc, C., Andrieux, A., & Job, D. (2003). STOP proteins. Biochemistry, 42, 12125–12132.

    Article  CAS  Google Scholar 

  14. Homma, T., Iwahashi, H., & Komatsu, Y. (2003). Yeast gene expression during growth at low temperature. Cryobiology, 46, 230–237.

    Article  CAS  Google Scholar 

  15. Thaisuchat, H., Baumann, M., Pontiller, J., Hesse, F., & Ernst, W. (2011). Identification of a novel temperature sensitive promoter in CHO cells. BMC Biotechnology, 11, 51.

    Article  CAS  Google Scholar 

  16. Danno, S., Nishiyama, H., Higashitsuji, H., Yokoi, H., Xue, J. H., Itoh, K., et al. (1997). Increased transcript level of RBM3, a member of the glycine-rich RNA-binding protein family, in human cells in response to cold stress. Biochemical and Biophysical Research Communications, 236, 804–807.

    Article  CAS  Google Scholar 

  17. Derry, J. M., Kerns, J. A., & Francke, U. (1995). RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain. Human Molecular Genetics, 4, 2307–2311.

    Article  CAS  Google Scholar 

  18. Dresios, J., Aschrafi, A., Owens, G. C., Vanderklish, P. W., Edelman, G. M., & Mauro, V. P. (2005). Cold stress-induced protein Rbm3 binds 60S ribosomal subunits, alters microRNA levels, and enhances global protein synthesis. Proceedings of the National Academy of Sciences of the United States of America, 102, 1865–1870.

    Article  CAS  Google Scholar 

  19. Smart, F., Aschrafi, A., Atkins, A., Owens, G. C., Pilotte, J., Cunningham, B. A., et al. (2007). Two isoforms of the cold-inducible mRNA-binding protein RBM3 localize to dendrites and promote translation. Journal of Neurochemistry, 101, 1367–1379.

    Article  CAS  Google Scholar 

  20. Nishiyama, H., Danno, S., Kaneko, Y., Itoh, K., Yokoi, H., Fukumoto, M., et al. (1998). Decreased expression of cold-inducible RNA-binding protein (CIRP) in male germ cells at elevated temperature. American Journal of Pathology, 152, 289–296.

    CAS  Google Scholar 

  21. Sonna, L. A., Fujita, J., Gaffin, S. L., & Lilly, C. M. (2002). Effects of heat and cold stress on mammalian gene expression. Journal of Applied Physiology, 92, 1725–1742.

    CAS  Google Scholar 

  22. Wellmann, S., Buhrer, C., Moderegger, E., Zelmer, A., Kirschner, R., Koehne, P., et al. (2004). Oxygen-regulated expression of the RNA-binding proteins RBM3 and CIRP by a HIF-1-independent mechanism. Journal of Cell Science, 117, 1785–1794.

    Article  CAS  Google Scholar 

  23. Al-Fageeh, M. B., & Smales, C. M. (2009). Cold-inducible RNA binding protein (CIRP) expression is modulated by alternative mRNAs. RNA, 15, 1164–1176.

    Article  CAS  Google Scholar 

  24. Coecke, S., Balls, M., Bowe, G., Davis, J., Gstraunthaler, G., Hartung, T., et al. (2005). Guidance on good cell culture practice. A report of the second ECVAM task force on good cell culture practice. Alternatives to Laboratory Animals, 33, 261–287.

    CAS  Google Scholar 

  25. Schreiber, E., Matthias, P., Muller, M. M., & Schaffner, W. (1989). Rapid detection of octamer binding proteins with ‘mini-extracts’, prepared from a small number of cells. Nucleic Acids Research, 17, 6419.

    Article  CAS  Google Scholar 

  26. Zwollo, P., & Desiderio, S. (1994). Specific recognition of the blk promoter by the B-lymphoid transcription factor B-cell-specific activator protein. Journal of Biological Chemistry, 269, 15310–15317.

    CAS  Google Scholar 

  27. Nishiyama, H., Itoh, K., Kaneko, Y., Kishishita, M., Yoshida, O., & Fujita, J. (1997). A glycine-rich RNA-binding protein mediating cold-inducible suppression of mammalian cell growth. Journal of Cell Biology, 137, 899–908.

    Article  CAS  Google Scholar 

  28. Cartharius, K., Frech, K., Grote, K., Klocke, B., Haltmeier, M., Klingenhoff, A., et al. (2005). MatInspector and beyond: Promoter analysis based on transcription factor binding sites. Bioinformatics, 21, 2933–2942.

    Article  CAS  Google Scholar 

  29. Ma, L., Larkin, M. A., Blackshields, G., Brown, N. P., Chenna, R., McGettigan, P. A., et al. (2007). ClustalW and ClustalX version 2.0. Bioinformatics, 23, 2947–2948.

    Article  Google Scholar 

  30. Frith, M. C., Fu, Y., Yu, L., Chen, J. F., Hansen, U., & Weng, Z. (2004). Detection of functional DNA motifs via statistical over-representation. Nucleic Acids Research, 32, 1372–1381.

    Article  CAS  Google Scholar 

  31. Muller, F., Demeny, M. A., & Tora, L. (2007). New problems in RNA polymerase II transcription initiation: Matching the diversity of core promoters with a variety of promoter recognition factors. Journal of Biological Chemistry, 282, 14685–14689.

    Article  Google Scholar 

  32. Mantovani, R. (1998). A survey of 178 NF-Y binding CCAAT boxes. Nucleic Acids Research, 26, 1135–1143.

    Article  CAS  Google Scholar 

  33. Fairchild, K. D., Singh, I. S., Patel, S., Drysdale, B. E., Viscardi, R. M., Hester, L., et al. (2004). Hypothermia prolongs activation of NF-kappaB and augments generation of inflammatory cytokines. American Journal of Physiology. Cell Physiology, 287, 422–431.

    Article  Google Scholar 

  34. Kent, W. J., Sugnet, C. W., Furey, T. S., Roskin, K. M., Pringle, T. H., Zahler, A. M., et al. (2002). The human genome browser at UCSC. Genome Research, 12, 996–1006.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to C. Mark Smales.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Al-Fageeh, M.B., Smales, C.M. Alternative Promoters Regulate Cold Inducible RNA-Binding (CIRP) Gene Expression and Enhance Transgene Expression in Mammalian Cells. Mol Biotechnol 54, 238–249 (2013). https://doi.org/10.1007/s12033-013-9649-5

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12033-013-9649-5

Keywords

Navigation