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Repeat-induced gene silencing in mammals
Abstract
In both plants and Drosophila melanogaster, expression from a transgenic locus may be silenced when repeated transgene copies are arranged as a concatameric array. This repeat-induced gene silencing is frequently manifested as a decrease in the proportion of cells that express the transgene, resulting in a variegated pattern of expression. There is also some indication that, in transgenic mammals, the number of transgene copies within an array can exert a repressive influence on expression, with several mouse studies reporting a decrease in the level of expression per copy as copy number increases. However, because these studies compare different sites of transgene integration as well as arrays with different numbers of copies, the expression levels observed may be subject to varying position effects as well as the influence of the multicopy array. Here we describe use of the lox/Cre system of site-specific recombination to generate transgenic mouse lines in which different numbers of a transgene are present at the same chromosomal location, thereby eliminating the contribution of position effects and allowing analysis of the effect of copy number alone on transgene silencing. Reduction in copy number results in a marked increase in expression of the transgene and is accompanied by decreased chromatin compaction and decreased methylation at the transgene locus. These findings establish that the presence of multiple homologous copies of a transgene within a concatameric array can have a repressive effect upon gene expression in mammalian systems.
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“This site of integration is neither centromeric nor telomeric, and so presumably the silencing is related to the multicopy nature of the transgene array [13,14].”
From A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development (2008) · cites this paper as [13]
In the citing paper
“transgene silencing,4”
From Adeno‐associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo†‡ (2010) · cites this paper as [4]
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The Mechanisms of Genomic Imprinting
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Lee, J.-W., Shin, S.-Y., Kim, H.-S., Jin, E., Lee, H., & Oh, H. (2017) · Algal Research · doi:10.1016/j.algal.2017.09.001 · Cited by 21
Genetically engineered birds; pre-CRISPR and CRISPR era
Dehdilani, N., Taemeh, S. Y., Goshayeshi, L., & Dehghani, H. (2021) · Biology of Reproduction · doi:10.1093/biolre/ioab196 · Cited by 21
Ruden, D. M., Jamison, D. C., Zeebèrg, B. R., Garfinkel, M. D., Weinstein, J. N., Rasouli, P., & Lu, X. (2008) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2007.12.004 · Cited by 21
“the rate of unmethylated CpG dinucleotides [37].”
Buzzelli, J. N., O’Connor, L., Scurr, M., Chin, S. C. N., Catubig, A., Ng, G. Z., Oshima, M., Oshima, H., Giraud, A. S., SUTTON, P. R. N., et al. (2018) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00304.2018 · Cited by 21
“Lines 2 and 3, which had high copy integrations (~38 and 20 copies, respectively), lacked transgene expression, likely due to repeat-induced gene silencing often associated with high copy transgene arrays (11).”
BackgroundMolecular Basis of Human Complement C1s Deficiency
Endo, Y., Kanno, K., Takahashi, M., Yamaguchi, K., Kohno, Y., & Fujita, T. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.4.2180 · Cited by 21
Differential regulation of laminin b1 transgene expression in the neonatal and adult mouse brain
Sharif, K. A., Baker, H. A., & Gudas, L. J. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.03.064 · Cited by 21
Banu, Y., Matsuda, M., Yoshihara, M., Kondo, M., Sutou, S., & Matsukuma, S. (2002) · Molecular Reproduction and Development · doi:10.1002/mrd.10035 · Cited by 21
Optimization of the Gal4/UAS transgenic tools in zebrafish
Zhang, Y., Ouyang, J., Qie, J., Zhang, G., Liu, L., & Yang, P. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-09591-0 · Cited by 20
Concatenation of Transgenic DNA: Random or Orchestrated?
Smirnov, A. V., & Баттулин, Н. Р. (2021) · Genes · doi:10.3390/genes12121969 · Cited by 19
Arce, J. D.-C., Göckel-Krzikalla, E., & Rösl, F. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr604 · Cited by 20
“Gene silencing in general is accompanied not only by increased DNA methylation, but also by a loss of DNase I hypersensitive sites, inability to recruit RNA polymerase II upon stimulation and increased methylation of histone H3 lysine 9 (H3K9), respectively (19).”
BackgroundHeritable L1 Retrotransposition Events During Development: Understanding Their Origins
Richardson, S. R., & Faulkner, G. J. (2018) · BioEssays · doi:10.1002/bies.201700189 · Cited by 20
Fraser, S. T., Isern, J., & Baron, M. H. (2010) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(10)76022-5 · Cited by 20
Kholodilov, N. G., Kim, S. R., Yarygina, O., Kareva, T., Cho, J. W., Baohan, A., & Burke, R. E. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07128.x · Cited by 19
“This phenomenon, referred to as ‘repeatinduced transgene silencing’ (Garrick et al. 1998) has been previously described (Allen et al.”
BackgroundRepeat-induced gene silencing of L1 transgenes is correlated with differential promoter methylation
Rosser, J. M., & An, W. (2010) · Gene · doi:10.1016/j.gene.2010.02.005 · Cited by 19
“Local heterochromatin formation is thought to be responsible for RIGS on tandem arrayed transgenes as the reduction in transgene copy number is accompanied by increased steady-state mRNA (Assaad et al., 1993; Ye and Signer, 1996; Garrick et al., 1998), higher chromatin accessibility (Ye and Signer, 1996; Garrick et al.”
BackgroundInfluentialDeletion of p21 (WAF-1/Cip1) Does Not Induce Systemic Autoimmunity in Female BXSB Mice
Lawson, B. R., Kono, D. H., & Theofilopoulos, A. N. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.11.5928 · Cited by 19
Kannan, M., Li, J., Fritz, S. E., Husarek, K. E., Sanford, J. C., Sullivan, T. L., Tiwary, P. K., An, W., Boeke, J. D., & Symer, D. E. (2017) · Mobile DNA · doi:10.1186/s13100-017-0091-2 · Cited by 19
“While multiple copies of a transgene frequently can recombine at a single genomic locus [69], individual copies of L1 reporter genes typically integrate at interspersed genomic sites.”
BackgroundPartition of Repeat-Induced Point Mutations Reveals Structural Aspects of Homologous DNA-DNA Pairing
Mazur, A. K., & Gladyshev, E. A. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2018.06.030 · Cited by 18
“During RIGS, newly integrated repetitive DNA sequences can trigger the formation of heterochromatin in organisms as diverse as plants (16), mammals (17), and filamentous fungi (18,19).”
BackgroundFinckenstein, F. G., Davicioni, E., Osborn, K. G., Cavenee, W. K., Arden, K. C., & Anderson, M. J. (2006) · Transgenic Research · doi:10.1007/s11248-006-9011-9 · Cited by 18
“Likely due to repeat-induced transgene silencing (Garrick et al. 1998), PAX3-FKHR could be carried ‘silently’ in male MP3-5 transgenic mice with no observable phenotype.”
BackgroundRole of inverted DNA repeats in transcriptional and post-transcriptional gene silencing
Muskens, M., Vissers, A. P. A., Mol, J. N. M., & Kooter, J. M. (2000) · Springer eBooks · doi:10.1007/978-94-011-4183-3_9 · Cited by 18
Enhancer-Dependent Transcriptional Oscillations in Mouse Erythroleukemia Cells
Feng, Y.-Q., Alami, R., & Bouhassira, E. E. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.7.4907 · Cited by 18
“In metazoans, the two best-studied such phenomena are heterochromatin-induced position effect variegation (PEV) (24), in which transgenes are clonally inactivated in a fraction of a cell population, and extinction of transgenes in cell culture (50) and transgenic animals ( 15 , 35, 41, 47).”
BackgroundStewart, S., MacDonald, N., Perkins, E. L., deJong, G., Perez, C. F., & Lindenbaum, M. H. (2002) · Gene Therapy · doi:10.1038/sj.gt.3301757 · Cited by 18
Sternfeld, M., Patrick, J., & Soreq, H. (1998) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(98)80028-4 · Cited by 18
Schmouth, J.-F., Bonaguro, R. J., Corso‐Díaz, X., & Simpson, E. M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002544 · Cited by 17
“The transgene can potentially lead to disruption of endogenous gene function and repeat-induced gene silencing, two factors that must be taken into account when generating mice by random-insertion pronuclear injection [42].”
BackgroundZou, Y., Dong, Y., Meng, Q., Zhao, Y., & Li, N. (2018) · Scientific Reports · doi:10.1038/s41598-018-21122-5 · Cited by 18
Metadata
- Authors
- Garrick, D., Fiering, S., Martin, D. I. K., & Whitelaw, E.
- Affiliations
- The University of Sydney (AU)
- Dartmouth–Hitchcock Medical Center (US)
- Fred Hutch Cancer Center (US)
- Venue
- Nature Genetics
- Published
- 1998-01
- Volume
- 18
- Issue
- 1
- Pages
- 56-59
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2065189089
- Cited by
- 887
- References
- 32
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 20 · 2023: 16 · 2022: 9 · 2021: 16 · 2020: 16 · 2019: 14 · 2018: 20 · 2017: 23 · 2016: 25 · 2015: 28 · 2014: 24 · 2013: 24 · 2012: 41
- FWCI
- 36.14
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Animal Genetics and Reproduction
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Keywords
- transgene copy number, transgene silencing, position effect, transgenic mice, chromatin condensation, DNA methylation, epigenetic silencing
- MeSH terms
- Animals, Chromatin, Erythrocytes, Female, Gene Expression Regulation, Humans, Lac Operon, Male, Mammals, Mice, Transgenic, Repetitive Sequences, Nucleic Acid, Transcription, Genetic, Viral Proteins, Gene Dosage, Transgenes, Integrases, Mice
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