MAR elements regulate the probability of epigenetic switching between active and inactive gene expression
Abstract
Gene expression often cycles between active and inactive states in eukaryotes, yielding variable or noisy gene expression in the short-term, while slow epigenetic changes may lead to silencing or variegated expression. Understanding how cells control these effects will be of paramount importance to construct biological systems with predictable behaviours. Here we find that a human matrix attachment region (MAR) genetic element controls the stability and heritability of gene expression in cell populations. Mathematical modeling indicated that the MAR controls the probability of long-term transitions between active and inactive expression, thus reducing silencing effects and increasing the reactivation of silent genes. Single-cell short-terms assays revealed persistent expression and reduced expression noise in MAR-driven genes, while stochastic burst of expression occurred without this genetic element. The MAR thus confers a more deterministic behavior to an otherwise stochastic process, providing a means towards more reliable expression of engineered genetic systems.
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MAR and UCOE helped decrease the variability of expression between different clones and contributed to maintaining an active transcriptional state for better transgene expression.
“It was also demonstrated that MAR and UCOE helped decrease the variability of expression between the different clones and contributed in maintaining an active transcriptional state for better transgene expression (Williams et al., 2005;Galbete et al., 2009;Harraghy et al., 2011).”
From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Galbete et al., 2009
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Stochastic protein expression in individual cells at the single molecule level
Cai, L., Friedman, N., & Xie, X. S. (2006) · Nature · doi:10.1038/nature04599 · Cited by 1,145 · see citing works
Repeat-induced gene silencing in mammals
Garrick, D., Fiering, S., Martin, D. I. K., & Whitelaw, E. (1998) · Nature Genetics · doi:10.1038/ng0198-56 · Cited by 887 · see citing works
Eissenberg, J. C., Morris, G. D., Reuter, G., & Hartnett, T. (1992) · Genetics · doi:10.1093/genetics/131.2.345 · Cited by 315 · 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
Harraghy, N., Calabrese, D., Fisch, I., Girod, P., LeFourn, V., Regamey, A., & Mermod, N. (2015) · Biotechnology Journal · doi:10.1002/biot.201400649 · Cited by 32 · see citing works
Self-citation
- Authors
- Luis Galbete, J., Buceta, M., & Mermod, N.
- Affiliations
- Institute of Biotechnology, University of Lausanne a , CH-1015 Lausanne Switzerland
- University of Lausanne (CH)
- Corresponding author
- Mermod, Nicolas
- ORCID
- Mermod, Nicolas
- Venue
- Molecular BioSystems
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-12-05
- Volume
- 5
- Issue
- 2
- Pages
- 143-150
- ISSN
- 1742-2051 (ISSN-L)
- 1742-206X
- OpenAlex
- W2011664376
- Cited by
- 35
- References
- 3
- Citations by year
- 2019: 3 · 2018: 2 · 2017: 1 · 2016: 1 · 2015: 5 · 2014: 4 · 2013: 8 · 2012: 1
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular BioSystems (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- matrix attachment regions, epigenetic switching, gene silencing, gene reactivation, stochastic gene expression, gene expression stability, heritability of gene expression, mathematical modeling of gene expression
- MeSH terms
- Animals, Cricetulus, Flow Cytometry, Gene Expression Regulation, Genetic Engineering, Cricetinae, Humans, Models, Theoretical, Time Factors, CHO Cells, Transgenes, Reverse Transcriptase Polymerase Chain Reaction, Gene Silencing, Epigenesis, Genetic, Matrix Attachment Regions
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