Reitz Diedre, Djeghmoum Yasmina, Watson Ruth A, Rajput Pallavi, Argueso Juan Lucas, Heyer Wolf-Dietrich, Piazza Aurèle
Department of Microbiology and Molecular Genetics, One Shields Ave, University of California, Davis, CA 95616, USA.
Univ Lyon, ENS, UCBL, CNRS, INSERM, Laboratory of Biology and Modelling of the Cell, UMR5239, U 1210, F-69364, Lyon, France.
bioRxiv. 2023 Mar 16:2023.03.15.532751. doi: 10.1101/2023.03.15.532751.
Punctuated bursts of structural genomic variations (SVs) have been described in various organisms, but their etiology remains incompletely understood. Homologous recombination (HR) is a template-guided mechanism of repair of DNA double-strand breaks and stalled or collapsed replication forks. We recently identified a DNA break amplification and genome rearrangement pathway originating from the endonucleolytic processing of a multi-invasion (MI) DNA joint molecule formed during HR. Genome-wide sequencing approaches confirmed that multi-invasion-induced rearrangement (MIR) frequently leads to several repeat-mediated SVs and aneuploidies. Using molecular and genetic analysis, and a novel, highly sensitive proximity ligation-based assay for chromosomal rearrangement quantification, we further delineate two MIR sub-pathways. MIR1 is a universal pathway occurring in any sequence context, which generates secondary breaks and frequently leads to additional SVs. MIR2 occurs only if recombining donors exhibit substantial homology, and results in sequence insertion without additional break or SV. The most detrimental MIR1 pathway occurs late on a subset of persisting DNA joint molecules in a PCNA/Polδ-independent manner, unlike recombinational DNA synthesis. This work provides a refined mechanistic understanding of these HR-based SV formation pathways and shows that complex repeat-mediated SVs can occur without displacement DNA synthesis. Sequence signatures for inferring MIR1 from long-read data are proposed.
在各种生物体中都已描述了结构性基因组变异(SVs)的间断性爆发,但其病因仍未完全明确。同源重组(HR)是一种由模板引导的修复DNA双链断裂以及停滞或崩溃的复制叉的机制。我们最近发现了一种DNA断裂扩增和基因组重排途径,其起源于HR过程中形成的多侵入(MI)DNA接头分子的核酸内切酶加工。全基因组测序方法证实,多侵入诱导的重排(MIR)经常导致几种重复介导的SVs和非整倍体。通过分子和遗传分析,以及一种用于染色体重排定量的新型、高灵敏度的基于邻近连接的检测方法,我们进一步描绘了两条MIR子途径。MIR1是一种在任何序列背景下都能发生的通用途径,它会产生二次断裂并经常导致额外的SVs。MIR2仅在重组供体表现出显著同源性时才会发生,并且会导致序列插入而无额外的断裂或SV。与重组性DNA合成不同,最有害的MIR1途径以不依赖PCNA/Polδ的方式在一部分持续存在的DNA接头分子上较晚发生。这项工作为这些基于HR的SV形成途径提供了更精确的机制理解,并表明复杂的重复介导的SVs可以在没有置换DNA合成的情况下发生。我们提出了从长读数据推断MIR1的序列特征。