Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Telomeric amplicons of SUL1 and Y' in yeast are generated by microhomology-mediated break induced replication occurring in cis.

Created on 21 Aug 2026

Authors

Bonita J Brewer, Rebecca Martin, Elizabeth Ramage, Celia Payen, Sara C Di Rienzi, Yang Zhao, Kelsey M Van Sickle, Jocelyn Verhey, Miranda Zalusky, Danny E Miller, Giang T Ong, Jamie L McKee, Gina M Alvino, Maitreya J Dunham, M K Raghuraman

Published in

PLoS genetics. Volume 22. Issue 8. Pages e1012214. Aug 20, 2026. Epub Aug 20, 2026.

Abstract

Gene amplification is a potent driver of evolution and is thought to contribute to genetic diseases, including cancer. The yeast Saccharomyces cerevisiae is a powerful organism for understanding amplification mechanisms. When yeast is grown long term in sulfate-limiting chemostats, amplification of the gene that encodes the primary sulfate transporter, SUL1, is a common outcome. Here we describe a form of SUL1 amplification in which multiple copies of the right terminal region of chromosome II are appended in tandem to a native telomere. We find this form of amplicon when we delete the origin of replication next to SUL1 or delete a variety of genes involved in DNA metabolism. It is the only form of amplification found in a yku70Δ mutant suggesting that telomeres are involved. We propose that these terminal addition events occur when a destabilized 3' G1-3T telomeric sequence invades a short (~7 bp) internal telomere sequence (ITS) to begin a form of microhomology-mediated break-induced replication (mmBIR) that has been documented in type-I survivors of telomerase mutants. In addition to amplification of the right end of chromosome II we also find that telomeres containing the sub-telomeric repeat Y' experience similar tandem amplification events and show that their formation is reduced in a pol32Δ mutant, a gene involved in mmBIR. Within individual amplicons the expanded ITSs and Y's are nearly identical, suggesting that the multiple copies of the amplified region are generated in a single mmBIR event that we describe as pseudo-rolling circle mmBIR. A similar amplification event at the P-telomere of human chromosome 18 has four copies of a ~ 54 kb region separated by ITSs of nearly identical size. This finding suggests that these additional copies of the terminal fragment of human chromosome 18 arose by the same pseudo-rolling circle mechanism, perhaps during a period of telomeric stress.

PMID:
42623421
Bibliographic data and abstract were imported from PubMed on 21 Aug 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 2
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement