Rad27/ <scp>FEN</scp> 1 prevents accumulation of Okazaki fragments and ribosomal <scp>DNA</scp> copy number changes

DNA copy number changes are the most frequent genomic alterations in cancer cells. Here, we demonstrate that Rad27/FEN1, a structure-specific nuclease in budding yeast, plays a crucial role in maintaining the stability of the ribosomal DNA (rDNA) repeats. Severe rDNA instability is observed in the rad27∆ mutant, independently of Fob1-mediated DNA replication fork arrest and DNA double-strand break (DSB) formation in the rDNA. The rad27Δ mutant accumulates Okazaki fragments in the rDNA region, without inducing the formation of detectable DSBs. Similar rDNA instability is observed in DNA ligase<sup>Cdc9</sup>-deficient cells. Furthermore, Exonuclease 1 and PCNA partially compensate for the loss of Rad27 in rDNA stabilization. These findings highlight the importance of proper Okazaki fragment maturation in the maintenance of rDNA stability.

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Publication Details

Journal
FEBS Letters
Published
2025-10-27
DOI
https://doi.org/10.1002/1873-3468.70193
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Rad27/ FEN 1 prevents accumulation of Okazaki fragments and ribosomal DNA copy number changes

Mariko Sasaki, Naoko Arata, T. Yamaji, Yuko Katayama
FEBS Letters
DNA Repair Mechanisms
article

Rad27/ FEN 1 prevents accumulation of Okazaki fragments and ribosomal DNA copy number changes

Mariko Sasaki, Naoko Arata, T. Yamaji, Yuko Katayama
article en

Abstract

DNA copy number changes are the most frequent genomic alterations in cancer cells. Here, we demonstrate that Rad27/FEN1, a structure-specific nuclease in budding yeast, plays a crucial role in maintaining the stability of the ribosomal DNA (rDNA) repeats. Severe rDNA instability is observed in the rad27∆ mutant, independently of Fob1-mediated DNA replication fork arrest and DNA double-strand break (DSB) formation in the rDNA. The rad27Δ mutant accumulates Okazaki fragments in the rDNA region, without inducing the formation of detectable DSBs. Similar rDNA instability is observed in DNA ligase<sup>Cdc9</sup>-deficient cells. Furthermore, Exonuclease 1 and PCNA partially compensate for the loss of Rad27 in rDNA stabilization. These findings highlight the importance of proper Okazaki fragment maturation in the maintenance of rDNA stability.

FEBS LettersVol. 599(24)
National Institute of Genetics (JP), The Graduate University for Advanced Studies, SOKENDAI (JP)
Research Organization of Information and Systems, Japan Society for the Promotion of Science
Openalex Percentile: Top 73%
DNA Repair Mechanisms
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