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- W2742893306 abstract "Bloom syndrome is a cancer predisposition disorder caused by mutations in the BLM helicase gene. Cells from persons with Bloom syndrome exhibit striking genomic instability characterized by excessive sister chromatid exchange events (SCEs). We applied single-cell DNA template strand sequencing (Strand-seq) to map the genomic locations of SCEs. Our results show that in the absence of BLM, SCEs in human and murine cells do not occur randomly throughout the genome but are strikingly enriched at coding regions, specifically at sites of guanine quadruplex (G4) motifs in transcribed genes. We propose that BLM protects against genome instability by suppressing recombination at sites of G4 structures, particularly in transcribed regions of the genome." @default.
- W2742893306 created "2017-08-17" @default.
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- W2742893306 date "2018-01-18" @default.
- W2742893306 modified "2023-10-10" @default.
- W2742893306 title "BLM helicase suppresses recombination at G-quadruplex motifs in transcribed genes" @default.
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- W2742893306 doi "https://doi.org/10.1038/s41467-017-02760-1" @default.
- W2742893306 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5773480" @default.
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