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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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“Repeat-induced gene silencing has been reported for conventional transgene tandem arrays ( Garrick et al., 1998 ).”
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“Similarly, mice generated with different copy numbers of a lacZ reporter gene at the same chromosome location only exhibited β-galactosidase activity if they carried small lacZ copy numbers: these were associated with low DNA methylation and decreased chromatin compaction [116].”
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“An additional FRT site was included upstream of the floxed neomycin cassette which provides the basis of the promoter switching in subsequent steps.”
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“Nevertheless, concomitant methylation and silencing of transgenic DNA repeats triggered by a high transgene copy number has suggested the possibility of a DNA repeats/RNAi gene silencing in mammals [110].”
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“The latter can result from insertions into existing heterochromatic regions that fail to support long-term gene expression, the assembly of heterochromatin on tandemly repeated transgene arrays [8], or homology-based silencing.”
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“Where many copies of a transgene lie in a tandem array within a single integration site the likelihood of gene silencing may increase since such arrays are subject to RIGS (Rosser and An 2010; Garrick et al. 1998).”
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“Together with the observation of variegated expression of transgenes in transgenic mice (Garrick et al., 1998; Ramirez et al., 2001), it is conceivable that the negative selection of tTA-expressing germ cells accompanied by the survival of germ cells with low or no expression of tTA results in the…”
BackgroundA Dominant Modifier of Transgene Methylation Is Mapped by QTL Analysis to Mouse Chromosome 13Preprint
Schaerly, P. V., Pickard, B. S., Walter, J., Jung, M., Pourcel, L., Reik, W., Gauguier, D., Vergnaud, G., & Pourcel, C. (2001) · Genome Research · doi:10.1101/gr.163801 · Cited by 9
“Transgenes carrying sequences of bacterial or viral origin and tandemly repeated sequences (Garrick et al. 1998) often appear to be the target for de novo methylation early in development.”
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Sperm DNA Methylation: Not a Vehicle for Dietary Reprogramming of Offspring?
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“Previous work has shown that a high number of copies can repress transgene expression, possibly because of the fact that highly repetitive DNA tends to fold into a heterochromatic structure (Garrick et al. 1998).”
BackgroundGenomic analysis of facioscapulohumeral muscular dystrophy
Clapp, J. (2003) · Briefings in Functional Genomics and Proteomics · doi:10.1093/bfgp/2.3.213 · Cited by 8
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Identification of ADPKD-Related Genes and Pathways in Cells Overexpressing PKD2
Zhang, Z., Dang, Y., Wang, Z., Wang, H., Pan, Y., & He, J. H. (2020) · Genes · doi:10.3390/genes11020122 · Cited by 7
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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