Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination
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Summary
It is suggested that illegitimate recombination is an important competing pathway with homologous recombination for chromosomal double-strand break repair in mammalian cells.
- Type
- article
- Published
- 1997-01-01
- Cited by
- 297
- References
- 37
- Access
- Open access
- OpenAlex
- https://openalex.org/W2099675208
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:26505605
Keywords
Homologous recombination, FLP-FRT recombination, Biology, Mitotic crossover, Non-allelic homologous recombination
References
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- Meiosis-induced double-strand break sites determined by yeast chromatin structure.
- Asymmetrical recognition and activity of the I‐SceI endonuclease on its site and on intron‐exon junctions.
- Analysis of the 3' end of the human pro-alpha 2(I) collagen gene. Utilization of multiple polyadenylation sites in cultured fibroblasts.
- Two different types of double-strand breaks in Saccharomyces cerevisiae are repaired by similar RAD52-independent, nonhomologous recombination events
- Direct-repeat analysis of chromatid interactions during intrachromosomal recombination in mouse cells
- DNA synthesis errors associated with double-strand-break repair.
- Introduction of double-strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease.
- Comparison of filler DNA at immune, nonimmune, and oncogenic rearrangements suggests multiple mechanisms of formation
- Site-specific recombination determined by I-SceI, a mitochondrial group I intron-encoded endonuclease expressed in the yeast nucleus.
- Construction of plasmids that express E. coli beta-galactosidase in mammalian cells.
- Homologous recombination in plant cells is enhanced by in vivo induction of double strand breaks into DNA by a site-specific endonuclease.
- Substrate recognition and induced DNA distortion by the PI-SceI endonuclease, an enzyme generated by protein splicing.
- Efficient modification of the APRT gene by FLP/FRT site-specific targeting
- A novel selection system for recombinational and mutational events within an intron of a eucaryotic gene.
- Spontaneous and restriction enzyme-induced chromosomal recombination in mammalian cells.
- A personal communication
- Structure of mutant alleles at the aprt locus of Chinese hamster ovary cells.
- Stimulation of intrachromosomal homologous recombination in human cells by electroporation with site-specific endonucleases.
- Deletion mapping of highly conserved transcribed sequence downstream fromAPRT locus
Cited by
- Construction of a recombinant adenovirus for efficient delivery of the I-SceI yeast endonuclease to human cells and its application in the in vivo cleavage of chromosomes to expose new potential telomeres.
- Homologous recombination in extrachromosomal plasmid substrates is not suppressed by p53.
- Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot
- Comparison of zinc finger nucleases for use in gene targeting in mammalian cells.
- The Contribution of DNA Interstrand Crosslinks to Aging
- Robust cell line development using meganucleases.
- Regulation of cellular signalling pathways by Adenovirus
- Function and application of TAL effectors
- Investigation of alternative approaches to narrow-leafed lupin (Lupinus angustifolius) genetic transformation
- Functional Characterisation of Human MUS81 Complexes
- Targeting therapeutic vector expression and integration for gene therapy applications
- DNA Repair Protocols
- Analysis of germline mutations induced by chemicals
- Impaired Cytogenetic Damage Repair and Cell Cycle Regulation in Response to Ionizing Radiation in Human Fibroblast Cells with Individual Knock-down of 25 Genes
- The role of epigenetics in the rat mammary gland
- Vieillissement vasculaire chez des patients athérosclérotiques: Sénescence prématurée des cellules endothéliales?
- Frequent chromosomal translocations induced by DNA double-strand breaks
- Proteomic analysis of DNA damage induced stress signaling with focus on p53 : S100A6 regulation, function and potential as biomarker in lung cancer and as a novel therapeutic target
- Targeted gene knockout mediated by triple helix forming oligonucleotides
- Gross deletions and translocations in human genetic disease.
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