Hanzlikova, Hana, Kalasova, Ilona, Demin, Annie, Pennicott, Lewis and Caldecott, Keith (2018) The importance of Poly(ADP-Ribose) Polymerase as a sensor of unligated Okazaki fragments during DNA replication. Molecular Cell, 71 (2). pp. 319-331. ISSN 1097-2765
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Abstract
The Importance of Poly(ADP-Ribose) Polymerase as a Sensor of Unligated Okazaki Fragments during DNA Replication.
Poly(ADP-ribose) is synthesized by PARP enzymes during the repair of stochastic DNA breaks. Surprisingly, however, we show that most if not all endogenous poly(ADP-ribose) is detected in normal S phase cells at sites of DNA replication. This S phase poly(ADP-ribose) does not result from damaged or misincorporated nucleotides or from DNA replication stress. Rather, perturbation of the DNA replication proteins LIG1 or FEN1 increases S phase poly(ADP-ribose) more than 10-fold, implicating unligated Okazaki fragments as the source of S phase PARP activity. Indeed, S phase PARP activity is ablated by suppressing Okazaki fragment formation with emetine, a DNA replication inhibitor that selectively inhibits lagging strand synthesis. Importantly, PARP activation during DNA replication recruits the single-strand break repair protein XRCC1, and human cells lacking PARP activity and/or XRCC1 are hypersensitive to FEN1 perturbation. Collectively, our data indicate that PARP1 is a sensor of unligated Okazaki fragments during DNA replication and facilitates their repair.
Item Type: | Article |
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Schools and Departments: | School of Life Sciences > Sussex Centre for Genome Damage and Stability |
Research Centres and Groups: | Genome Damage and Stability Centre |
Depositing User: | Paula Amiet-West |
Date Deposited: | 13 Jul 2018 11:36 |
Last Modified: | 24 Jul 2018 12:10 |
URI: | http://srodev.sussex.ac.uk/id/eprint/77126 |
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📧 Request an updateProject Name | Sussex Project Number | Funder | Funder Ref |
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Cellular and Pathological Responses to Chromosomal DNA Single-Strand Breaks | G2053 | MRC-MEDICAL RESEARCH COUNCIL | MR/P010121/1 |
Non-homologous End-Joining Protein Complexes and Genome Stability | G1305 | CANCER RESEARCH UK | C6563/A16771 |
SIDSCA: Defective DNA Damage Responses in Dominant Neurodegenerative Diseases | G1930 | EUROPEAN UNION | 694996 |
An Integrated drug discovery and validation platform for the identification of novel agents targeting DNA damage response for the treatment of cancer. | G1902 | Wellcome Trust | 110578/Z/15/Z |