Genome instability triggers intercellular DNA transfer between human cells
Summary
The mammalian genome is safeguarded within the confines of the interphase nucleus. However, genomic instability can trigger the mislocalization of nuclear DNA to the cytoplasm within micronuclei or as fragmented chromosomes. Beyond activating cell-autonomous signaling programs, whether such cytoplasmic DNA can elicit non-cell-autonomous consequences to nearby cells remains unclear. Here, we show that cytoplasmic DNAs undergo intercellular transfer through contact-dependent, cytoskeleton-ba
Content
# Genome instability triggers intercellular DNA transfer between human cells
*Published: 2026 May 19*
The mammalian genome is safeguarded within the confines of the interphase
nucleus. However, genomic instability can trigger the mislocalization of nuclear
DNA to the cytoplasm within micronuclei or as fragmented chromosomes. Beyond
activating cell-autonomous signaling programs, whether such cytoplasmic DNA can
elicit non-cell-autonomous consequences to nearby cells remains unclear. Here,
we show that cytoplasmic DNAs undergo intercellular transfer through
contact-dependent, cytoskeleton-based nanotube structures connecting adjacent
human cells. Diverse sources of genomic instability-including exposure to
mitotic spindle poisons, ionizing radiation, and Cas9-induced chromosome
breakage-promote nanotube-mediated DNA transfer in both cancerous and
non-cancerous cells. Transferred DNA fragments are stably inherited as
functional extrachromosomal genetic elements in the recipient host genome,
thereby conferring heritable phenotypic traits to the recipient cell. Our
findings uncover a horizontal gene transfer-like mechanism through which direct
cell-cell contact can propagate genomic instability and reshape mammalian
genomes.
DOI: 10.1016/j.cell.2026.04.041