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Human Molecular Genetics Advance Access published online on June 11, 2009

Human Molecular Genetics, doi:10.1093/hmg/ddp279
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© The Author 2009. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells

Hiroki Kurahashi1,2,*, Hidehito Inagaki1, Takema Kato1,2, Eriko Hosoba1, Hiroshi Kogo1, Tamae Ohye1, Makiko Tsutsumi1, Hasbaira Bolor1, Maoqing Tong1 and Beverly S. Emanuel3

1 Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan 2 Development Center for Targeted and Minimally Invasive Diagnosis and Treatment, Fujita Health University, Toyoake, Aichi 470-1192, Japan 3 Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104; Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA

* Corresponding author: Hiroki Kurahashi, M.D. Ph.D., Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi 470-1192, Japan, Phone: +81-562-93-9391, Fax: +81-562-93-8831, email: kura{at}fujita-hu.ac.jp

Received May 7, 2009; Revised June 9, 2009; Accepted June 9, 2009

Palindromic regions are unstable and susceptible to deletion in prokaryotes and eukaryotes possibly due to stalled or slow replication. In the human genome, they also appear to become partially or completely deleted, while two palindromic AT-rich repeats (PATRR) contribute to known recurrent constitutional translocations. To explore the mechanism that causes the development of palindrome instabilities in humans, we compared the incidence of de novo translocations and deletions at PATRRs in human cells. Using a highly sensitive PCR assay that can detect single molecules, de novo deletions were detected neither in human somatic cells nor in sperm. However, deletions were detected at low frequency in cultured cell lines. Inhibition of DNA replication by administration of siRNA against the DNA polymerase alpha 1 (POLA1) gene or introduction of POLA inhibitors increased the frequency. This is in contrast to PATRR-mediated translocations that were never detected in similar conditions but were observed frequently in human sperm samples. Further, deletions were found to take place during both leading and lagging strand synthesis. Our data suggest that stalled or slow replication induces deletions within PATRRs, but that other mechanisms might contribute to PATRR-mediated recurrent translocations in humans.


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