Menu

Javascript is not activated in your browser. This website needs javascript activated to work properly.
You are here

Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.

Author:
  • Young Seok Ju
  • Jose M C Tubio
  • William Mifsud
  • Beiyuan Fu
  • Helen R Davies
  • Manasa Ramakrishna
  • Yilong Li
  • Lucy Yates
  • Gunes Gundem
  • Patrick S Tarpey
  • Sam Behjati
  • Elli Papaemmanuil
  • Sancha Martin
  • Anthony Fullam
  • Moritz Gerstung
  • Jyoti Nangalia
  • Anthony R Green
  • Carlos Caldas
  • Åke Borg
  • Andrew Tutt
  • Ming Ta Michael Lee
  • Laura J Van't Veer
  • Benita K T Tan
  • Samuel Aparicio
  • Paul N Span
  • John W M Martens
  • Stian Knappskog
  • Anne Vincent-Salomon
  • Anne-Lise Børresen-Dale
  • Jórunn Erla Eyfjörd
  • Adrienne M Flanagan
  • Christopher Foster
  • David E Neal
  • Colin Cooper
  • Rosalind Eeles
  • Sunil R Lakhani
  • Christine Desmedt
  • Gilles Thomas
  • Andrea L Richardson
  • Colin A Purdie
  • Alastair M Thompson
  • Ultan McDermott
  • Fengtang Yang
  • Serena Nik-Zainal
  • Peter J Campbell
  • Michael R Stratton
Publishing year: 2015
Language: English
Pages: 814-824
Publication/Series: Genome Research
Volume: 25
Issue: 6
Document type: Journal article
Publisher: Cold Spring Harbor Laboratory Press

Abstract english

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.

Keywords

  • Genetics

Other

Published
  • CREATE Health
  • ISSN: 1549-5469
Åke Borg
Åke Borg
E-mail: ake.borg [at] med.lu.se

Principal investigator

Oncology and Pathology, MV

+46 46 275 25 52

MV 404 C21B2

90

Project manager

Familial Breast Cancer

90

Professor

Oncology and Pathology, MV

MV 404 C21C2

90