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Chromosome Structure and Dynamics

Recombination at Long Mutant Telomeres Produces Tiny Single- and Double-Stranded Telomeric Circles

, , , &
Pages 4406-4412 | Received 06 Jan 2005, Accepted 07 Mar 2005, Published online: 27 Mar 2023
 

Abstract

Recombinational telomere elongation (RTE) known as alternate lengthening of telomeres is the mechanism of telomere maintenance in up to 5 to 10% of human cancers. The telomeres of yeast mutants lacking telomerase can also be maintained by recombination. Previously, we proposed the roll-and-spread model to explain this elongation in the yeast Kluveromyces lactis. This model suggests that a very small (∼100-bp) circular molecule of telomeric DNA is copied by a rolling circle event to generate a single long telomere. The sequence of this primary elongated telomere is then spread by recombination to all remaining telomeres. Here we show by two-dimensional gel analysis and electron microscopy that small circles of single- and double-stranded telomeric DNA are commonly made by recombination in a K. lactis mutant with long telomeres. These circles were found to be especially abundant between 100 and 400 bp (or nucleotides). Interestingly, the single-stranded circles consist of only the G-rich telomeric strand sequence. To our knowledge this is the first report of single-stranded telomeric circles as a product of telomere dysfunction. We propose that the small telomeric circles form through the resolution of an intratelomeric strand invasion which resembles a t-loop. Our data reported here demonstrate that K. lactis can, in at least some circumstances, make telomeric circles of the very small sizes predicted by the roll-and-spread model. The very small circles seen here are both predicted products of telomere rapid deletion, a process observed in both human and yeast cells, and predicted templates for roll-and-spread RTE.

ACKNOWLEDGMENTS

We thank Gary Fielding for his help with figure preparations.

Grants from both the National Institutes of Health (CGM61645 and GM31819) and the Ellison Foundation have supported this work. J.D.G. is an Ellison Senior Scholar. Cindy Groff-Vindman is supported through a training grant from the National Institutes of Health (5T32GMOO&10330).

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