학술논문

Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Document Type
article
Source
Genome Research. 25(6)
Subject
Biochemistry and Cell Biology
Genetics
Biological Sciences
Stem Cell Research - Nonembryonic - Human
Human Genome
Stem Cell Research
Cancer
1.1 Normal biological development and functioning
Underpinning research
Aetiology
2.1 Biological and endogenous factors
Generic health relevance
Amino Acid Sequence
Cell Line
Tumor
Cell Nucleus
Chromosomes
DNA Copy Number Variations
DNA End-Joining Repair
DNA Replication
DNA
Mitochondrial
Genome
Human
Genome
Mitochondrial
HeLa Cells
Humans
In Situ Hybridization
Fluorescence
Mitochondria
Molecular Sequence Data
Neoplasms
Reproducibility of Results
Sequence Analysis
DNA
ICGC Prostate Cancer Working Group
ICGC Bone Cancer Working Group
ICGC Breast Cancer Working Group
Hela Cells
Medical and Health Sciences
Bioinformatics
Language
Abstract
Mitochondrial genomes are separated from the nuclear genome for most of the cell cycle by the nuclear double membrane, intervening cytoplasm, and the mitochondrial double membrane. Despite these physical barriers, we show that somatically acquired mitochondrial-nuclear genome fusion sequences are present in cancer cells. Most occur in conjunction with intranuclear genomic rearrangements, and the features of the fusion fragments indicate that nonhomologous end joining and/or replication-dependent DNA double-strand break repair are the dominant mechanisms involved. Remarkably, mitochondrial-nuclear genome fusions occur at a similar rate per base pair of DNA as interchromosomal nuclear rearrangements, indicating the presence of a high frequency of contact between mitochondrial and nuclear DNA in some somatic cells. Transmission of mitochondrial DNA to the nuclear genome occurs in neoplastically transformed cells, but we do not exclude the possibility that some mitochondrial-nuclear DNA fusions observed in cancer occurred years earlier in normal somatic cells.