BTRR complex deficiency is a driver for genomic instability in Bloom syndrome

Gönenc, I. I., Wolff, A., Busley, A. V., Wieland, A., Tijhuis, A., Müller, C., Wardenaar, R., Argyriou, L., Kaulfuss, S., Räschle, M., et al.

10.1101/2025.04.17.649287 · was preprinted

discovery

Surfaced because: matches the platform's topic region.

relevance 0.34 openness 0.00 novelty 0.45

Abstract

Biallelic loss-of-function (LoF) variants in the BTRR complex members BLM, TOP3A, RMI1, and RMI2 cause Bloom syndrome (BSyn). The BTRR complex mainly acts on DNA replication and DNA repair processes, and dysfunction of this complex underlies the increased genomic instability and cancer predisposition associated with the BSyn phenotype. Here, we report CRISPR/Cas9-based genome-edited isogenic induced pluripotent stem cell (iPSC) models with compound heterozygous LoF variants in BLM, TOP3A, and RMI1. The cellular phenotype of all three BTRR-deficient iPSC lines included chromosome segregation defects, increased sister chromatid exchange rates, and impaired DNA single-strand template repair. Using single-cell whole genome sequencing, we showed that BTRR complex deficiency causes increased genome copy number alterations (CNAs) and, therefore, is a driver for genomic instability. CNA load was further induced by applying replication stress, and we observed that BTRRKO iPSCs acquired fewer de novo CNA events compared to wild-type cells, suggesting a possible selection loss against cells with high levels of DNA damage. Importantly, stress-induced and non-stress-induced CNAs in single-cell genomes were not stochastically distributed throughout the genome, but instead enriched at fragile sites. This finding might offer an opportunity for the development of novel NGS-based approaches to measure rates of genomic instability in disease conditions.

Lifecycle

biorxiv v2 2026-08-31 source ↗

Discussion

No qualifying discussion yet.