Article ID Journal Published Year Pages File Type
2039167 Cell Reports 2015 7 Pages PDF
Abstract

•Yeast interstitial telomeric sequences (ITSs) are prone to expansions•Post-replicative repair and homologous recombination contribute to ITS instability•These data can explain length polymorphism characteristic of ITSs in humans•The proposed model may have implications for alternative telomere lengthening in cancer

SummaryTelomeric repeats located within chromosomes are called interstitial telomeric sequences (ITSs). They are polymorphic in length and are likely hotspots for initiation of chromosomal rearrangements that have been linked to human disease. Using our S. cerevisiae system to study repeat-mediated genome instability, we have previously shown that yeast telomeric (Ytel) repeats induce various gross chromosomal rearrangements (GCR) when their G-rich strands serve as the lagging strand template for replication (G orientation). Here, we show that interstitial Ytel repeats in the opposite C orientation prefer to expand rather than cause GCR. A tract of eight Ytel repeats expands at a rate of 4 × 10−4 per replication, ranking them among the most expansion-prone DNA microsatellites. A candidate-based genetic analysis implicates both post-replication repair and homologous recombination pathways in the expansion process. We propose a model for Ytel repeat expansions and discuss its applications for genome instability and alternative telomere lengthening (ALT).

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