Pathways and assays for DNA double-strand break repair by homologous recombination
- PMID: 31294447
- DOI: 10.1093/abbs/gmz076
Pathways and assays for DNA double-strand break repair by homologous recombination
Abstract
Double strand breaks (DSBs) are the most detrimental type of DNA damage that must be repaired to ensure genome integrity and cell survival. Unrepaired or improperly repaired DSBs can potentially cause tumorigenesis or cell death. DSBs are primarily repaired by non-homologous end joining or homologous recombination (HR). The HR pathway is initiated by processing of the 5'-end of DSBs to generate 3'-end single-strand DNA (ssDNA). Furthermore, the intermediate is channeled to one of the HR sub-pathways, including: (i) double Holliday junction (dHJ) pathway, (ii) synthesis-dependent strand annealing (SDSA), (iii) break-induced replication (BIR), and (iv) single-strand annealing (SSA). In the dHJ sub-pathway, the 3'-ssDNA coated with Rad51 recombinase performs homology search and strand invasion, forming a displacement loop (D-loop). Capture of the second end by the D-loop generates a dHJ intermediate that is subsequently dissolved by DNA helicase or resolved by nucleases, producing non-crossover or crossover products. In SDSA, the newly synthesized strand is displaced from the D-loop and anneals to the end on the other side of the DSBs, producing non-crossovers. In contrast, BIR repairs one-end DSBs by copying the sequence up to the end of the template chromosome, resulting in translocation or loss of heterozygosity. SSA takes place when resection reveals flanking homologous repeats that can anneal, leading to deletion of the intervening sequences. A variety of reporter assays have been developed to monitor distinct HR sub-pathways in both Saccharomyces cerevisiae and mammals. Here, we summarize the principles and representative assays for different HR sub-pathways with an emphasis on the studies in the budding yeast.
Keywords: break-induced replication; double-strand break; homologous recombination; single-strand annealing; synthesis-dependent strand annealing.
© The Author(s) 2019. Published by Oxford University Press on behalf of the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Similar articles
-
Annealing of Complementary DNA Sequences During Double-Strand Break Repair in Drosophila Is Mediated by the Ortholog of SMARCAL1.Genetics. 2017 May;206(1):467-480. doi: 10.1534/genetics.117.200238. Epub 2017 Mar 3. Genetics. 2017. PMID: 28258182 Free PMC article.
-
Homologous recombination via synthesis-dependent strand annealing in yeast requires the Irc20 and Srs2 DNA helicases.Genetics. 2012 May;191(1):65-78. doi: 10.1534/genetics.112.139105. Epub 2012 Feb 23. Genetics. 2012. PMID: 22367032 Free PMC article.
-
The requirement for recombination factors differs considerably between different pathways of homologous double-strand break repair in somatic plant cells.Plant J. 2012 Dec;72(5):781-90. doi: 10.1111/j.1365-313X.2012.05119.x. Epub 2012 Oct 1. Plant J. 2012. PMID: 22860689
-
Homologous Recombination-Mediated DNA Repair and Implications for Clinical Treatment of Repair Defective Cancers.Methods Mol Biol. 2019;1999:3-29. doi: 10.1007/978-1-4939-9500-4_1. Methods Mol Biol. 2019. PMID: 31127567 Review.
-
Investigations of homologous recombination pathways and their regulation.Yale J Biol Med. 2013 Dec 13;86(4):453-61. Yale J Biol Med. 2013. PMID: 24348209 Free PMC article. Review.
Cited by
-
PROTACs in Ovarian Cancer: Current Advancements and Future Perspectives.Int J Mol Sci. 2024 May 7;25(10):5067. doi: 10.3390/ijms25105067. Int J Mol Sci. 2024. PMID: 38791105 Free PMC article. Review.
-
Targeting DNA damage response as a potential therapeutic strategy for head and neck squamous cell carcinoma.Front Oncol. 2022 Oct 21;12:1031944. doi: 10.3389/fonc.2022.1031944. eCollection 2022. Front Oncol. 2022. PMID: 36338767 Free PMC article. Review.
-
Division of Labor by the HELQ, BLM, and FANCM Helicases during Homologous Recombination Repair in Drosophila melanogaster.Genes (Basel). 2022 Mar 8;13(3):474. doi: 10.3390/genes13030474. Genes (Basel). 2022. PMID: 35328029 Free PMC article.
-
KAT5 histone acetyltransferase mutations in cancer cells.MicroPubl Biol. 2022 Nov 28;2022:10.17912/micropub.biology.000676. doi: 10.17912/micropub.biology.000676. eCollection 2022. MicroPubl Biol. 2022. PMID: 36530474 Free PMC article.
-
The Emerging Role of OTUB2 in Diseases: From Cell Signaling Pathway to Physiological Function.Front Cell Dev Biol. 2022 Mar 2;10:820781. doi: 10.3389/fcell.2022.820781. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35309903 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials