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DNA synthesis generates terminal duplications that seal end-to-end chromosome fusions.


ABSTRACT: End-to-end chromosome fusions that occur in the context of telomerase deficiency can trigger genomic duplications. For more than 70 years, these duplications have been attributed solely to breakage-fusion-bridge cycles. To test this hypothesis, we examined end-to-end fusions isolated from Caenorhabditis elegans telomere replication mutants. Genome-level rearrangements revealed fused chromosome ends having interrupted terminal duplications accompanied by template-switching events. These features are very similar to disease-associated duplications of interstitial segments of the human genome. A model termed Fork Stalling and Template Switching has been proposed previously to explain such duplications, where promiscuous replication of large, noncontiguous segments of the genome occurs. Thus, a DNA synthesis-based process may create duplications that seal end-to-end fusions, in the absence of breakage-fusion-bridge cycles.

SUBMITTER: Lowden MR 

PROVIDER: S-EPMC4154375 | biostudies-literature | 2011 Apr

REPOSITORIES: biostudies-literature

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DNA synthesis generates terminal duplications that seal end-to-end chromosome fusions.

Lowden Mia Rochelle MR   Flibotte Stephane S   Moerman Donald G DG   Ahmed Shawn S  

Science (New York, N.Y.) 20110401 6028


End-to-end chromosome fusions that occur in the context of telomerase deficiency can trigger genomic duplications. For more than 70 years, these duplications have been attributed solely to breakage-fusion-bridge cycles. To test this hypothesis, we examined end-to-end fusions isolated from Caenorhabditis elegans telomere replication mutants. Genome-level rearrangements revealed fused chromosome ends having interrupted terminal duplications accompanied by template-switching events. These features  ...[more]

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