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PLOS ONE  2012 

In vivo Importance of Homologous Recombination DNA Repair for Mouse Neural Stem and Progenitor Cells

DOI: 10.1371/journal.pone.0037194

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Abstract:

We characterized the in vivo importance of the homologous recombination factor RAD54 for the developing mouse brain cortex in normal conditions or after ionizing radiation exposure. Contrary to numerous homologous recombination genes, Rad54 disruption did not impact the cortical development without exogenous stress, but it dramatically enhanced the radiation sensitivity of neural stem and progenitor cells. This resulted in the death of all cells irradiated during S or G2, whereas the viability of cells irradiated in G1 or G0 was not affected by Rad54 disruption. Apoptosis occurred after long arrests at intra-S and G2/M checkpoints. This concerned every type of neural stem and progenitor cells, showing that the importance of Rad54 for radiation response was linked to the cell cycle phase at the time of irradiation and not to the differentiation state. In the developing brain, RAD54-dependent homologous recombination appeared absolutely required for the repair of damages induced by ionizing radiation during S and G2 phases, but not for the repair of endogenous damages in normal conditions. Altogether our data support the existence of RAD54-dependent and -independent homologous recombination pathways.

References

[1]  Gal JS, Morozov YM, Ayoub AE, Chatterjee M, Rakic P, et al. (2006) Molecular and morphological heterogeneity of neural precursors in the mouse neocortical proliferative zones. J Neurosci 26: 1045–1056.
[2]  Pontious A, Kowalczyk T, Englund C, Hevner RF (2008) Role of intermediate progenitor cells in cerebral cortex development. Dev Neurosci 30: 24–32.
[3]  Stancik EK, Navarro-Quiroga I, Sellke R, Haydar TF (2010) Heterogeneity in ventricular zone neural precursors contributes to neuronal fate diversity in the postnatal neocortex. J Neurosci 30: 7028–7036.
[4]  Miyata T, Kawaguchi A, Saito K, Kawano M, Muto T, et al. (2004) Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells. Development 131: 3133–3145.
[5]  Haubensak W, Attardo A, Denk W, Huttner WB (2004) Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis. Proc Natl Acad Sci U S A 101: 3196–3201.
[6]  Sauer ME, Walker BE (1959) Radioautographic study of interkinetic nuclear migration in the neural tube. Proc Soc Exp Biol Med 101: 557–560.
[7]  Sidman RL, Miale IL, Feder N (1959) Cell proliferation and migration in the primitive ependymal zone: an autoradiographic study of histogenesis in the nervous system. Exp Neurol 1: 322–333.
[8]  Murciano A, Zamora J, Lopez-Sanchez J, Frade JM (2002) Interkinetic nuclear movement may provide spatial clues to the regulation of neurogenesis. Mol Cell Neurosci 21: 285–300.
[9]  Del Bene F, Wehman AM, Link BA, Baier H (2008) Regulation of neurogenesis by interkinetic nuclear migration through an apical-basal notch gradient. Cell 134: 1055–1065.
[10]  Latasa MJ, Cisneros E, Frade JM (2009) Cell cycle control of Notch signaling and the functional regionalization of the neuroepithelium during vertebrate neurogenesis. Int J Dev Biol 53: 895–908.
[11]  Aguilera A, Gomez-Gonzalez B (2008) Genome instability: a mechanistic view of its causes and consequences. Nat Rev Genet 9: 204–217.
[12]  McKinnon PJ (2004) ATM and ataxia telangiectasia. EMBO Rep 5: 772–776.
[13]  Barzilai A, Biton S, Shiloh Y (2008) The role of the DNA damage response in neuronal development, organization and maintenance. DNA Repair (Amst) 7: 1010–1027.
[14]  Hoeijmakers JH (2001) Genome maintenance mechanisms for preventing cancer. Nature 411: 366–374.
[15]  Nowak E, Etienne O, Millet P, Lages CS, Mathieu C, et al. (2006) Radiation-induced H2AX phosphorylation and neural precursor apoptosis in the developing brain of mice. Radiat Res 165: 155–164.
[16]  Herzog KH, Chong MJ, Kapsetaki M, Morgan JI, McKinnon PJ (1998) Requirement for Atm in ionizing radiation-induced cell death in the developing central nervous system. Science 280: 1089–1091.
[17]  D'Sa-Eipper C, Leonard JR, Putcha G, Zheng TS, Flavell RA, et al. (2001) DNA damage-induced neural precursor cell apoptosis requires p53 and caspase 9 but neither Bax nor caspase 3. Development 128: 137–146.
[18]  Roque T, Haton C, Etienne O, Chicheportiche A, Rousseau L, et al. (2012) Lack of a p21(waf1/cip) -Dependent G1/S Checkpoint in Neural Stem and Progenitor Cells After DNA Damage in vivo. Stem Cells. 30(3): 537–47.
[19]  Lieber MR, Ma Y, Pannicke U, Schwarz K (2003) Mechanism and regulation of human non-homologous DNA end-joining. Nat Rev Mol Cell Biol 4: 712–720.
[20]  Hartlerode AJ, Scully R (2009) Mechanisms of double-strand break repair in somatic mammalian cells. Biochem J 423: 157–168.
[21]  Shibata A, Conrad S, Birraux J, Geuting V, Barton O, et al. (2011) Factors determining DNA double-strand break repair pathway choice in G2 phase. EMBO J 30: 1079–1092.
[22]  Lim DS, Hasty P (1996) A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53. Mol Cell Biol 16: 7133–7143.
[23]  Ludwig T, Chapman DL, Papaioannou VE, Efstratiadis A (1997) Targeted mutations of breast cancer susceptibility gene homologs in mice: lethal phenotypes of Brca1, Brca2, Brca1/Brca2, Brca1/p53, and Brca2/p53 nullizygous embryos. Genes Dev 11: 1226–1241.
[24]  Orii KE, Lee Y, Kondo N, McKinnon PJ (2006) Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development. Proc Natl Acad Sci U S A 103: 10017–10022.
[25]  Frappart PO, Lee Y, Lamont J, McKinnon PJ (2007) BRCA2 is required for neurogenesis and suppression of medulloblastoma. EMBO J 26: 2732–2742.
[26]  Sii-Felice K, Barroca V, Etienne O, Riou L, Hoffschir F, et al. (2008) Role of Fanconi DNA repair pathway in neural stem cell homeostasis. Cell Cycle 7: 1911–1915.
[27]  Sii-Felice K, Etienne O, Hoffschir F, Mathieu C, Riou L, et al. (2008) Fanconi DNA repair pathway is required for survival and long-term maintenance of neural progenitors. EMBO J 27: 770–781.
[28]  Mazin AV, Mazina OM, Bugreev DV, Rossi MJ (2010) Rad54, the motor of homologous recombination. DNA Repair (Amst) 9: 286–302.
[29]  Raschle M, Van Komen S, Chi P, Ellenberger T, Sung P (2004) Multiple interactions with the Rad51 recombinase govern the homologous recombination function of Rad54. J Biol Chem 279: 51973–51980.
[30]  Petukhova G, Stratton S, Sung P (1998) Catalysis of homologous DNA pairing by yeast Rad51 and Rad54 proteins. Nature 393: 91–94.
[31]  Alexeev A, Mazin A, Kowalczykowski SC (2003) Rad54 protein possesses chromatin-remodeling activity stimulated by the Rad51-ssDNA nucleoprotein filament. Nat Struct Biol 10: 182–186.
[32]  Solinger JA, Kiianitsa K, Heyer WD (2002) Rad54, a Swi2/Snf2-like recombinational repair protein, disassembles Rad51:dsDNA filaments. Mol Cell 10: 1175–1188.
[33]  Bugreev DV, Mazina OM, Mazin AV (2006) Rad54 protein promotes branch migration of Holliday junctions. Nature 442: 590–593.
[34]  Essers J, Hendriks RW, Swagemakers SM, Troelstra C, de Wit J, et al. (1997) Disruption of mouse RAD54 reduces ionizing radiation resistance and homologous recombination. Cell 89: 195–204.
[35]  Bezzubova O, Silbergleit A, Yamaguchi-Iwai Y, Takeda S, Buerstedde JM (1997) Reduced X-ray resistance and homologous recombination frequencies in a RAD54?/? mutant of the chicken DT40 cell line. Cell 89: 185–193.
[36]  Takahashi T, Nowakowski RS, Caviness VS (1992) BUdR as an S-phase marker for quantitative studies of cytokinetic behaviour in the murine cerebral ventricular zone. J Neurocytol 21: 185–197.
[37]  Englund C, Fink A, Lau C, Pham D, Daza RA, et al. (2005) Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex. J Neurosci 25: 247–251.
[38]  Arai Y, Pulvers JN, Haffner C, Schilling B, Nusslein I, et al. (2011) Neural stem and progenitor cells shorten S-phase on commitment to neuron production. Nat Commun 2: 154.
[39]  Daboussi F, Courbet S, Benhamou S, Kannouche P, Zdzienicka MZ, et al. (2008) A homologous recombination defect affects replication-fork progression in mammalian cells. J Cell Sci 121: 162–166.
[40]  Shibata K, Ajiro K (1993) Cell cycle-dependent suppressive effect of histone H1 on mitosis-specific H3 phosphorylation. J Biol Chem 268: 18431–18434.
[41]  Essers J, van Steeg H, de Wit J, Swagemakers SM, Vermeij M, et al. (2000) Homologous and non-homologous recombination differentially affect DNA damage repair in mice. EMBO J 19: 1703–1710.
[42]  Takahashi T, Nowakowski RS, Caviness VS (1995) The cell cycle of the pseudostratified ventricular epithelium of the embryonic murine cerebral wall. J Neurosci 15: 6046–6057.
[43]  Lee Y, McKinnon PJ (2007) Responding to DNA double strand breaks in the nervous system. Neuroscience 145: 1365–1374.
[44]  Baye LM, Link BA (2007) Interkinetic nuclear migration and the selection of neurogenic cell divisions during vertebrate retinogenesis. J Neurosci 27: 10143–10152.
[45]  Gatz SA, Ju L, Gruber R, Hoffmann E, Carr AM, et al. (2011) Requirement for DNA Ligase IV during Embryonic Neuronal Development. J Neurosci 31: 10088–10100.
[46]  Tanori M, Pasquali E, Leonardi S, Giardullo P, Di Majo V, et al. (2011) Opposite modifying effects of HR and NHEJ deficiency on cancer risk in Ptc1 heterozygous mouse cerebellum. Oncogene.
[47]  Gottipati P, Vischioni B, Schultz N, Solomons J, Bryant HE, et al. (2010) Poly(ADP-ribose) polymerase is hyperactivated in homologous recombination-defective cells. Cancer Res 70: 5389–5398.
[48]  Stephan AK, Kliszczak M, Dodson H, Cooley C, Morrison CG (2011) Roles of vertebrate Smc5 in sister chromatid cohesion and homologous recombinational repair. Mol Cell Biol 31: 1369–1381.
[49]  Wesoly J, Agarwal S, Sigurdsson S, Bussen W, Van Komen S, et al. (2006) Differential contributions of mammalian Rad54 paralogs to recombination, DNA damage repair, and meiosis. Mol Cell Biol 26: 976–989.
[50]  Eppink B, Tafel AA, Hanada K, van Drunen E, Hickson ID, et al. (2011) The response of mammalian cells to UV-light reveals Rad54-dependent and independent pathways of homologous recombination. DNA Repair (Amst) 10: 1095–1105.
[51]  Takata M, Sasaki MS, Sonoda E, Morrison C, Hashimoto M, et al. (1998) Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells. EMBO J 17: 5497–5508.
[52]  Rothkamm K, Kruger I, Thompson LH, Lobrich M (2003) Pathways of DNA double-strand break repair during the mammalian cell cycle. Mol Cell Biol 23: 5706–5715.
[53]  Shrivastav M, De Haro LP, Nickoloff JA (2008) Regulation of DNA double-strand break repair pathway choice. Cell Res 18: 134–147.
[54]  Heyer WD, Kohli J (1994) Homologous recombination. Experientia 50: 189–191.

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