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bioRxiv · 10.64898/2026.02.28.708716

Microhomology-Mediated Tandem Duplication Drives Tandem Repeat Formation Across Life

Wei, X.·Gong, W.·Zheng, Y.·Zhang, J.·Peng, C.·He, X.·Jiang, C.
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Abstract

Tandem repeats (TR) are common genomic elements that are highly variable and with major functional consequences. Yet, the evolutionary trajectory for their formation remains poorly understood. One proposed mechanism is microhomology-mediated tandem duplication (MTD), in which single-copy DNA segments flanked by microhomology undergo tandem duplication (TD) and can further expand into TRs. Although MTD was first identified in the fission yeast Schizosaccharomyces pombe, its universal occurrence and postulated role in TR evolution have not been established. Using whole-genome deep sequencing and new analytical tools, we show that MTDs occur de novo universally across bacteria, archaea, fungi, and viruses. Further analysis of 2,245 reference genomes and millions of isolate genomes from 103 prokaryotic and eukaryotic microbial species, combined with human population TD data, somatic-germline mutations, and disease-associated variants, reveals that MTDs are consistently the dominant TD-forming mechanism across domains of life. Evidence suggests that MTDs have initiated the formation of the majority of existing TRs in genomes. Importantly, MTDs also prevail in human pathogenic TR mutations, including those linked to cancers. Mechanistically, deletion of the conserved mutator gene Rad27 specifically increased de novo MTD frequency in the budding yeast Saccharomyces cerevisiae, implicating Rad27-mediated Okazaki fragment maturation in MTD formation. These findings establish MTD as a universal and functionally significant mechanism for TR genesis. Graphic abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=121 SRC="FIGDIR/small/708716v1_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@db9ff1org.highwire.dtl.DTLVardef@e1a14corg.highwire.dtl.DTLVardef@124be79org.highwire.dtl.DTLVardef@15531ea_HPS_FORMAT_FIGEXP M_FIG C_FIG Significance StatementMicrohomology-mediated tandem duplications (MTDs) represent a universal mechanism driving tandem repeat formation across all domains of life--from viruses to humans. These duplications initiate genome evolution by expanding into functional tandem repeats and are the predominant form of pathogenic tandem duplications in human cancers and heritable disorders. Critically, disruption of the conserved Okazaki fragment processing pathway promotes MTD formation, establishing a fundamental link between DNA replication fidelity and genomic plasticity.

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Wei, X., Gong, W., Zheng, Y., Zhang, J., Peng, C., He, X., Jiang, C.. 2026-03-02. Microhomology-Mediated Tandem Duplication Drives Tandem Repeat Formation Across Life. https://doi.org/10.64898/2026.02.28.708716

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