| Literature DB >> 15377784 |
Albino Bacolla1, Adam Jaworski, Jacquelynn E Larson, John P Jakupciak, Nadia Chuzhanova, Shaun S Abeysinghe, Catherine D O'Connell, David N Cooper, Robert D Wells.
Abstract
Genomic rearrangements are a frequent source of instability, but the mechanisms involved are poorly understood. A 2.5-kbp poly(purine.pyrimidine) sequence from the human PKD1 gene, known to form non-B DNA structures, induced long deletions and other instabilities in plasmids that were mediated by mismatch repair and, in some cases, transcription. The breakpoints occurred at predicted non-B DNA structures. Distance measurements also indicated a significant proximity of alternating purine-pyrimidine and oligo(purine.pyrimidine) tracts to breakpoint junctions in 222 gross deletions and translocations, respectively, involved in human diseases. In 11 deletions analyzed, breakpoints were explicable by non-B DNA structure formation. We conclude that alternative DNA conformations trigger genomic rearrangements through recombination-repair activities.Entities:
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Year: 2004 PMID: 15377784 PMCID: PMC521098 DOI: 10.1073/pnas.0405974101
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205