Author
Listed:
- Lingchuan Hu
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- Tae Moon Kim
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- Mi Young Son
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- Sung-A Kim
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- Cory L. Holland
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- Satoshi Tateishi
(Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Honjo 2-2-1 Kumamoto 860-0811, Japan)
- Dong Hyun Kim
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- P. Renee Yew
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
- Cristina Montagna
(Albert Einstein College of Medicine of Yeshiva University)
- Lavinia C. Dumitrache
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA
Present address: Department of Genetics & Tumor Cell Biology M/S 331, St Jude Children’s Research Hospital, 262 Danny Thomas Place, Memphis, Tennessee 38105, USA.)
- Paul Hasty
(The Barshop Institute for Longevity and Aging Studies, The University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245-3207, USA)
Abstract
Stalling of replication forks in sequences that have non-allelic repeats can lead to genomic rearrangements; here two pathways consistent with homologous recombination and error-free post-replication repair fuse identical and mismatched repeats, respectively, thus inducing chromosomal rearrangements in mouse embryonic stem cells.
Suggested Citation
Lingchuan Hu & Tae Moon Kim & Mi Young Son & Sung-A Kim & Cory L. Holland & Satoshi Tateishi & Dong Hyun Kim & P. Renee Yew & Cristina Montagna & Lavinia C. Dumitrache & Paul Hasty, 2013.
"Two replication fork maintenance pathways fuse inverted repeats to rearrange chromosomes,"
Nature, Nature, vol. 501(7468), pages 569-572, September.
Handle:
RePEc:nat:nature:v:501:y:2013:i:7468:d:10.1038_nature12500
DOI: 10.1038/nature12500
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