User:BertoHContreras/DNA end resection

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DNA end resection, also called 5′–3′ degradation, is a biochemical process where the blunt end of a section of double-stranded DNA is modified by cutting away some nucleotides from the 5' end to produce a 3' single-stranded sequence[1][2].

Lesions in chromosomal DNA trigger DNA damage response in any phase of cell replication, but the natural ends of the linear chromosome are packed into complex specialized DNA protective packages called telomeres that prevent DNA repair activities[3][4]. Telomeres and DSBs have different functionality, but both experience the same 5′–3′ degradation process. The presence of a section of single-stranded DNA (ssDNA) allows the broken end of the DNA to line up accurately with a matching sequence, so that it can be accurately repaired.[1]

This figure describes the mechanism of DNA end resection at DSBs and Telomeres[3].

Background[edit]

A double-strand break (DSB) is a kind of DNA damage in which both strands in the double helix are severed. DSBs only occur during DNA replication of the cell cycle. They are particularly dangerous, because they can lead to genome rearrangements and instability[5]. Cases where two complementary strands are linked at the point of the DSB have potential to be catastrophic, such that the cell will not be able to complete mitosis when it next divides, and will either die or, in rare cases, undergo chromosomal loss, duplications, and even mutations[6][7]. Three mechanisms exist to repair DSBs: non-homologous end joining (NHEJ), Microhomology-mediated end joining (MMEJ), and homologous recombination HR[8][9][10]. Of these, only NHEJ does not rely on end resection[11].

DSBs can arise unexpectedly following exposure to endogenous and exogenous agents at unpredictable locations thought-out eukaryotic cells, but DSBs are standard mediators in meiotic recombination and allow for genome arrangements in yeast, such as switching mating-types in budding yeast[3][12]. DSBs can also emerge during DNA replication, where DNA Polymerase I encounters errors in the template or secondary strand[3].

Mechanism[edit]

Accurate repair of DSBs are essential in the upkeep of genome integrity. From the three mechanisms that exists to repair DSBs, NHEJ and HR repair mechanisms are the dominant pathways[4]. Several highly conservative proteins trigger the DNA Damage Checkpoint for detection of DSBs ensuing repair by either NHEJ or HR repair pathways. NHEJ mechanism functions in ligating two different DSBs with high fidelity, while HR relies on a homologous template to repair DSB ends[3][4]. DSBs occur at any point of the cell cycle, but DNA end resection HR pathway only occurs at two specific phases: S and G2 phases[3][4]. While DSBs happen in other phases of the cell cycle, DNA end resection is inhibited by other proteins allowing for only NHEJ repair mechanism to occur. Since HR pathway requires sister chromatids for activation, this event only happens in the G2 and S phases of the cell cycle during replication.

Before resection can take place, the break needs to be detected. In animals, this detection is done by PARP1[13]; similar systems exist in other eukaryotes: in plants, PARP2 seems to play this role[14]. PARP binding then recruits the MRN complex to the breakage site[15]. This is a highly conserved complex consisting of Mre11, Rad50 and NBS1 (known as Nibrin[16] in mammals, or Xrs2 in yeast, where this complex is called the MRX complex).

Before resection can start, CtBP1-interacting protein (CtIP) needs to bind to the MRN complex so that the first phase of resection can begin, namely short-range end resection. After phosphorylated CtIP binds, the Mre11 subunit is able to cut the 5'-terminated strand endonucleolytically, probably about 300 base pairs from the end[17][18], and then acts as a 3'→5' exonuclease to strip away the end of the 5' strand[18].

Resection of Telomere DSBs[edit]

Linear chromosomes are packed into complex specialized DNA protective packages called telomeres. Telomeres are short tandem DNA repeats and DSBs have different functionality, such that telomeres prevent DNA repair activities[3]. During telomeric DNA replication in the S/G2 and G1 phases of the cell cycle, the 3' lagging strand leaves a short overhang called a G-tail[3][4]. Telomeric DNA ends at the 3' G tail because the 3' lagging strand extends without its complimentary 5' C leading strand. The G tails provide a major function to telomeric DNA such that the G tails control telomere homeostasis[4].

Telomeres in G1 Phase[edit]

In the G1 phase of the cell cycle, the telomere-associated proteins RIF1, RIF2, and RAP2 bind to telomeric DNA and prevent access to the MRX complex[3][4]. Such process in S. Cerevisiae is negatively regulated by this activity. The MRX complex and the Ku complex bind simultaneously and independently to DSBs ends. In the presence of the telomere-associated proteins, MRX fails to bind to the DSB ends while the Ku complex binds to DSB ends. The bound Ku complex to the DSB ends protect the telomeres from nucleolytic degradation by exo1. This results in an inhibition of telomerase elongation at the DSB ends and prevents further telomere action at the G1 phase of the cell cycle.

Telomeres in the Late S/G2 Phase[edit]

In the late S/G2 phase of the cell cycle, the telomere-associated proteins RIF1, RIF2, and RAP2 exhibit their inhibitory effect by binding to telomeric DNA[3]. In the Late S/G2 phase, the protein kinase CDK1 (cyclin-dependent) promotes telomeric resection[3][4]. This control is exerted by cyclin-dependent kinases, which phosphorylate parts of the resection machinery[19]. This process alleviates the inhibitory effect of the telomere-associated proteins, and allows Cdc13 (a binding protein on both the lagging strand, and leading strand) to cover telomeric DNA. The binding of Cdc13 to DNA suppresses DNA damage checkpoint and allows resection to occur while allowing for telomerase elongation at the DSB ends[3].

Resection of Mitotic DSBs[edit]

One of the important regulatory controls in mitotic cells is deciding which specific DSB repair pathway to take. Once a DSB is detected, the highly conserved complexes are recruited by the DNA ends. If the cell is in the G1 phase of the cell cycle, the complex Ku prevents resection to occur and triggers the NHEJ pathway factors[3]. DSBs in the NHEJ pathway are ligated, a step in the NHEJ pathway that requires DNA ligase activity of Dnl4-Lif1/XRCC4 heterodimer and the Nej1/XLF protein[3]. This process results in error-prone religation of DSB ends at the G1 phase of the cell cycle.

If the cells are and S/G2 phase, Mitotic DSBs are controlled through Cdk1 activity and involves phosphorylation of Sae2 Ser267[3][4]. After phosphorylation occurs by Cdk1, MRX complex binds to dsDNA ends and generates short ssDNA that stretches in the 5' direction. The 5' ssDNA continues resection by the activity of the helicase enzyme, Sgs1 enzyme, and the nucleases Exo1 and Dna2. Involvement of Sae2 Sar267 in DSB processing is highly conserved throughout eukaryotes, such that the Sae2 along with the MRX complex are involved in two major functions: single-strand annealing, and processing of hairpin DNA structures[4]. Like all single-stranded DNA in the nucleus, the resected region is first coated by Replication protein A (RPA) complex[17][20], but RPA is then replaced with RAD51 to form a nucleoprotein filament which can take part in the search for a matching region, allowing HR to take place[17]. The 3' ssDNA coated by a RPA promotes the recruitment of Mec1. Mec1 further phosphorylates Sae2 along with Cdk1. The resulting phosphorylation by Sae2 by Mec1 helps increase the effect of resection and this in turn leads to the DNA damage checkpoint activation[3][4].

Positive and Negative Regulators of DNA Resection[edit]

Positive and Negative Regulators of the NHEJ Pathway[edit]

DNA end resection is key in determining the correct pathway either NHEJ or HR. For NHEJ pathway to occur, positive regulators such as the Ku and MRX complex mediate recruitment of other NHEJ-associated proteins such as Tel1, Lif1, Dnl4, and Nej1[3]. Since NHEJ does not rely on end resection, NHEJ could only happen in the G1 phase of the cell cycle. Both Ku and NHEJ-associated proteins prevent initiation of resection. Resection ensures that DSBs are not repaired by NHEJ (which joins broken DNA ends together without ensuring that they match), but rather by methods based on homology (matching DNA sequences). Because homologous recombination needs an intact copy of the DNA sequence (a sister chromatid) to be readily available. Cyclin-dependent protein kinase such as Cdk1 in yeast serves as a negative regulator of the NHEJ pathway[3]. Any activity associated with the presence of cyclin dependent protein kinases inhibit the NHEJ pathway. In S. Cerevisiae, the absence of phosphorylated Sae2 Ser267 inhibits the DNA end resection resulting in the NHEJ pathway[4].

Positive and Negative Regulators of the HR Pathway[edit]

The presence of a section of single-stranded DNA (ssDNA) allows the broken end of the DNA to line up accurately with a matching sequence, so that it can be accurately repaired. For HR pathway to occur in the S and G2 phases of the cell cycle, availability of repair template is required. 5′–3′ resection automatically links a DSB to HR[12]. Cycling-dependent protein kinase such as Cdk1 serve as a positive regulator of the HR pathway[3][4]. This positive regulator promotes The presence of this positive regulators promotes 5′–3′ nucleolytic degradation of DNA ends. MRX complex, and Spo11-induced DSBs along with Cdk1 activity serve as a positive regulator to the HR pathway[21]. Although Cdk1 activity serve as a promoter for the HR pathway leading to end resection, the absence of Cdk1 is a negative regulator in the HR channel.

See also[edit]

References[edit]

  1. ^ a b Jimeno S, Mejías-Navarro F, Prados-Carvajal R, Huertas P (2019). Donev R (ed.). "Controlling the balance between chromosome break repair pathways". Advances in Protein Chemistry and Structural Biology. 115 (First ed.). Cambridge, MA, United States: 95–134 (106). doi:10.1016/bs.apcsb.2018.10.004. ISBN 978-0-12-815560-8. PMID 30798939.
  2. ^ Liu T, Huang J (June 2016). "DNA End Resection: Facts and Mechanisms". Genomics, Proteomics & Bioinformatics. 14 (3): 126–130. doi:10.1016/j.gpb.2016.05.002. PMC 4936662. PMID 27240470.
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  8. ^ Huertas P (January 2010). "DNA resection in eukaryotes: deciding how to fix the break". Nature Structural & Molecular Biology. 17 (1): 11–6. doi:10.1038/nsmb.1710. PMC 2850169. PMID 20051983.
  9. ^ Liang L, Deng L, Chen Y, Li GC, Shao C, Tischfield JA (September 2005). "Modulation of DNA end joining by nuclear proteins". The Journal of Biological Chemistry. 280 (36): 31442–9. doi:10.1074/jbc.M503776200. PMID 16012167.
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  11. ^ Liu T, Huang J (June 2016). "DNA End Resection: Facts and Mechanisms". Genomics, Proteomics & Bioinformatics. 14 (3): 126–130. doi:10.1016/j.gpb.2016.05.002. PMC 4936662. PMID 27240470.
  12. ^ a b Liu, Ting; Huang, Jun (2016-6). "DNA End Resection: Facts and Mechanisms". Genomics, Proteomics & Bioinformatics. 14 (3): 126–130. doi:10.1016/j.gpb.2016.05.002. ISSN 1672-0229. PMC 4936662. PMID 27240470. {{cite journal}}: Check date values in: |date= (help)
  13. ^ Ray Chaudhuri A, Nussenzweig A (October 2017). "The multifaceted roles of PARP1 in DNA repair and chromatin remodelling". Nature Reviews. Molecular Cell Biology. 18 (10): 610–621. doi:10.1038/nrm.2017.53. PMC 6591728. PMID 28676700.
  14. ^ Song J, Keppler BD, Wise RR, Bent AF (May 2015). McDowell JM (ed.). "PARP2 Is the Predominant Poly(ADP-Ribose) Polymerase in Arabidopsis DNA Damage and Immune Responses". PLOS Genetics. 11 (5): e1005200. doi:10.1371/journal.pgen.1005200. PMC 4423837. PMID 25950582.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  15. ^ Haince JF, McDonald D, Rodrigue A, Déry U, Masson JY, Hendzel MJ, Poirier GG (January 2008). "PARP1-dependent kinetics of recruitment of MRE11 and NBS1 proteins to multiple DNA damage sites". The Journal of Biological Chemistry. 283 (2): 1197–208. doi:10.1074/jbc.M706734200. PMID 18025084. S2CID 6914911.
  16. ^ Uhrhammer N, Bay JO, Gatti RA (October 2002). "NBN (Nijmegen breakage syndrome 1)". Atlas of Genetics and Cytogenetics in Oncology and Haematology - NBS1. Retrieved 2008-02-12.
  17. ^ a b c Casari E, Rinaldi C, Marsella A, Gnugnoli M, Colombo CV, Bonetti D, Longhese MP (2019-06-07). "Processing of DNA Double-Strand Breaks by the MRX Complex in a Chromatin Context". Frontiers in Molecular Biosciences. 6: 43. doi:10.3389/fmolb.2019.00043. PMC 6567933. PMID 31231660.
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  19. ^ Casari E, Rinaldi C, Marsella A, Gnugnoli M, Colombo CV, Bonetti D, Longhese MP (2019-06-07). "Processing of DNA Double-Strand Breaks by the MRX Complex in a Chromatin Context". Frontiers in Molecular Biosciences. 6: 43. doi:10.3389/fmolb.2019.00043. PMC 6567933. PMID 31231660.
  20. ^ Chen C (2013). New research directions in DNA repair. Croatia: InTech. ISBN 978-953-51-1114-6. OCLC 957280914.
  21. ^ Xue, Chaoyou; Wang, Weibin; Crickard, J. Brooks; Moevus, Corentin J.; Kwon, Youngho; Sung, Patrick; Greene, Eric C. (2019-03-26). "Regulatory control of Sgs1 and Dna2 during eukaryotic DNA end resection". Proceedings of the National Academy of Sciences. 116 (13): 6091–6100. doi:10.1073/pnas.1819276116. ISSN 0027-8424. PMID 30850524.
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