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PMID: 42643946 Published · epublish English

Rad51 strand invasion function is needed for its role in CCTG tetranucleotide DNA repeat contractions.

microPublication biology ·Vol. 2026

Rutkowski SA, Serumaga NV, Bond EJ, Kim JC

Abstract

Myotonic Dystrophy Type 2 is a genetic disorder caused by expanded CCTG DNA repeats in the CNBP gene. By using a genetic assay in Saccharomyces cerevisiae and knocking out RAD51 , we previously found that homologous recombination is involved in large-scale CCTG repeat contractions. In this study, we measured contraction rates using the RAD51-II3A allele, which is defective in homology search and strand invasion. We found that the mean contraction rate in the RAD51-II3A strain was indistinguishable from rad51Δ , indicating that structural properties alone of the repetitive CCTG sequence cannot initiate double strand break repair by promoting strand invasion.

Article Info
Journal
microPublication biology
Abbr.
MicroPubl Biol
ISSN
2578-9430
Language
English
Country/Region
United States
NLM ID
101759238
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