Nanostructure of DNA repair foci revealed by superresolution microscopy

Induction of DNA double‐strand breaks (DSBs) by ionizing radiation leads to formation of micrometersized DNA‐repair foci, whose organization on the nanometer‐scale remains unknown because of the diffraction limit (~200 nm) of conventional microscopy. Here, we applied diffraction‐unlimited, direct stochastic optical‐reconstruction microscopy (dSTORM) with a lateral resolution of ~20 nm to analyze the focal nanostructure of the DSB marker histone γH2AX and the DNA‐repair protein kinase (DNA‐PK) in irradiated glioblastoma multiforme cells. Although standard confocal microscopy revealed substantial colocalization of immunostained γH2AX and DNA‐PK, in our dSTORM images, the 2 proteins showed very little (if any) colocalization despite their close spatial proximity. We also found that γH2AX foci consisted of distinct circular subunits (“nanofoci”) with a diameter of ~45 nm, whereas DNA‐PK displayed a diffuse, intrafocal distribution. We conclude that γH2AX nanofoci represent the elementary, structural units of DSB repair foci, that is, individual γH2AX‐containing nucleosomes. dSTORM‐based γH2AX nanofoci counting and distance measurements between nanofoci provided quantitative information on the total amount of chromatin involved in DSB repair as well as on the number and longitudinal distribution of γH2AX‐containing nucleosomes in a chromatin fiber. We thus estimate that a single focus involves between ~0.6 and ~1.1Mbp of chromatin, depending on radiation treatment. Because of their ability to unravel the nanostructure of DSB‐repair foci, dSTORM and related single‐molecule localization nanoscopy methods will likely emerge as powerful tools in biology and medicine to elucidate the effects of DNA damaging agents in cells.—Sisario, D., Memmel, S., Doose, S., Neubauer, J., Zimmermann, H., Flentje, M., Djuzenova, C. S., Sauer, M., Sukhorukov, V. L. Nanostructure of DNA repair foci revealed by superresolution microscopy. FASEB J. 32, 6469–6477 (2018). www.fasebj.org

[1]  D. Chan,et al.  The DNA-dependent Protein Kinase Is Inactivated by Autophosphorylation of the Catalytic Subunit (*) , 1996, The Journal of Biological Chemistry.

[2]  E. Rogakou,et al.  Megabase Chromatin Domains Involved in DNA Double-Strand Breaks in Vivo , 1999, The Journal of cell biology.

[3]  S. Nakajima,et al.  Differential phosphorylation of DNA-PKcs regulates the interplay between end-processing and end-ligation during nonhomologous end-joining. , 2015, Molecular cell.

[4]  R. Fietkau,et al.  Distinct increased outliers among 136 rectal cancer patients assessed by γH2AX , 2015, Radiation Oncology.

[5]  J. Hancock,et al.  On the use of Ripley's K-function and its derivatives to analyze domain size. , 2009, Biophysical journal.

[6]  M. Svetlova,et al.  Mechanism of elimination of phosphorylated histone H2AX from chromatin after repair of DNA double-strand breaks. , 2010, Mutation research.

[7]  D. Rhodes Chromatin structure: The nucleosome core all wrapped up , 1997, Nature.

[8]  Mike Heilemann,et al.  Super-resolution fluorescence imaging of chromosomal DNA. , 2012, Journal of structural biology.

[9]  S. Jackson,et al.  A new method for high-resolution imaging of Ku foci to decipher mechanisms of DNA double-strand break repair , 2013, The Journal of cell biology.

[10]  W. Bonner,et al.  γ-H2AX in Cancer Cells: A Potential Biomarker for Cancer Diagnostics, Prediction and Recurrence , 2006, Cell cycle.

[11]  Sarah Aufmkolk,et al.  Investigating cellular structures at the nanoscale with organic fluorophores. , 2013, Chemistry & biology.

[12]  E. Rogakou,et al.  DNA Double-stranded Breaks Induce Histone H2AX Phosphorylation on Serine 139* , 1998, The Journal of Biological Chemistry.

[13]  M. Heilemann,et al.  Subdiffraction-resolution fluorescence imaging with conventional fluorescent probes. , 2008, Angewandte Chemie.

[14]  Mike Heilemann,et al.  Live-cell super-resolution imaging with trimethoprim conjugates , 2010, Nature Methods.

[15]  Low level phosphorylation of histone H2AX on serine 139 (γH2AX) is not associated with DNA double-strand breaks , 2016, Oncotarget.

[16]  J. Turchi,et al.  Unraveling the Complexities of DNA-Dependent Protein Kinase Autophosphorylation , 2014, Molecular and Cellular Biology.

[17]  M. Flentje,et al.  Cell Surface Area and Membrane Folding in Glioblastoma Cell Lines Differing in PTEN and p53 Status , 2014, PLoS ONE.

[18]  S. Lees-Miller,et al.  Autophosphorylation of DNA-Dependent Protein Kinase Regulates DNA End Processing and May Also Alter Double-Strand Break Repair Pathway Choice , 2005, Molecular and Cellular Biology.

[19]  Takeo Ohnishi,et al.  Does γH2AX foci formation depend on the presence of DNA double strand breaks , 2005 .

[20]  Michel Nussenzweig,et al.  H2AX: the histone guardian of the genome. , 2004, DNA repair.

[21]  V. Bezrookove,et al.  A minority of foci or pan-nuclear apoptotic staining of γH2AX in the S phase after UV damage contain DNA double-strand breaks , 2010, Proceedings of the National Academy of Sciences.

[22]  K. McManus,et al.  ATM-dependent DNA damage-independent mitotic phosphorylation of H2AX in normally growing mammalian cells. , 2005, Molecular biology of the cell.

[23]  M. Durante,et al.  Identification of the elementary structural units of the DNA damage response , 2017, Nature Communications.

[24]  Yves Pommier,et al.  The complexity of phosphorylated H2AX foci formation and DNA repair assembly at DNA double-strand breaks , 2010, Cell cycle.

[25]  B. Ripley Modelling Spatial Patterns , 1977 .

[26]  E. Soutoglou,et al.  DNA damage response in the absence of DNA lesions continued… , 2009, Cell cycle.

[27]  E. Stelzer,et al.  A macrodomain-containing histone rearranges chromatin upon sensing PARP1 activation , 2009, Nature Structural &Molecular Biology.

[28]  Anthony W. Parker,et al.  The dynamics of Ku70/80 and DNA-PKcs at DSBs induced by ionizing radiation is dependent on the complexity of damage , 2012, Nucleic acids research.

[29]  M. Sauer,et al.  rapidSTORM: accurate, fast open-source software for localization microscopy , 2012, Nature Methods.

[30]  S. Hartmann,et al.  Actin cytoskeleton organization, cell surface modification and invasion rate of 5 glioblastoma cell lines differing in PTEN and p53 status. , 2015, Experimental cell research.

[31]  Y. Shiloh,et al.  Chromatin relaxation in response to DNA double-strand breaks is modulated by a novel ATM- and KAP-1 dependent pathway , 2006, Nature Cell Biology.

[32]  Louise Fairall,et al.  EM measurements define the dimensions of the "30-nm" chromatin fiber: evidence for a compact, interdigitated structure. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Christian Rübe,et al.  DNA repair in the context of chromatin: new molecular insights by the nanoscale detection of DNA repair complexes using transmission electron microscopy. , 2011, DNA repair.

[34]  M. Sauer,et al.  Photometry unlocks 3D information from 2D localization microscopy data , 2016, Nature Methods.

[35]  J. Reindl,et al.  Chromatin organization revealed by nanostructure of irradiation induced γH2AX, 53BP1 and Rad51 foci , 2017, Scientific Reports.

[36]  Mingzhu Wang,et al.  Cryo-EM Study of the Chromatin Fiber Reveals a Double Helix Twisted by Tetranucleosomal Units , 2014, Science.

[37]  A. Gudkov,et al.  Pseudo-DNA damage response in senescent cells , 2009, Cell cycle.

[38]  J. Bewersdorf,et al.  H2AX chromatin structures and their response to DNA damage revealed by 4Pi microscopy , 2006, Proceedings of the National Academy of Sciences.

[39]  V. Yamazaki,et al.  A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage , 2000, Current Biology.

[40]  Burkhard Jakob,et al.  Autophosphorylation of DNA-PKCS regulates its dynamics at DNA double-strand breaks , 2007, The Journal of cell biology.

[41]  A. Shibata,et al.  SETDB1, HP1 and SUV39 promote repositioning of 53BP1 to extend resection during homologous recombination in G2 cells , 2015, Nucleic acids research.

[42]  Sabrina Rossberger,et al.  Superresolution light microscopy shows nanostructure of carbon ion radiation‐induced DNA double‐strand break repair foci , 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[43]  T. Richmond,et al.  The structure of DNA in the nucleosome core , 2003, Nature.

[44]  M. Sung,et al.  A Macrohistone Variant Links Dynamic Chromatin Compaction to BRCA1-Dependent Genome Maintenance , 2014, Cell reports.

[45]  Markus Sauer,et al.  Migration pattern, actin cytoskeleton organization and response to PI3K-, mTOR-, and Hsp90-inhibition of glioblastoma cells with different invasive capacities , 2017, Oncotarget.

[46]  R. Kanaar,et al.  Analysis of ionizing radiation-induced foci of DNA damage repair proteins. , 2005, Mutation research.

[47]  Sebastian van de Linde,et al.  Live-cell dSTORM with SNAP-tag fusion proteins. , 2011, Nature methods.

[48]  E. Thompson,et al.  Compromized DNA repair as a basis for identification of cancer radiotherapy patients with extreme radiosensitivity. , 2016, Cancer letters.

[49]  A. El-Osta,et al.  Evaluation of the efficacy of radiation-modifying compounds using γH2AX as a molecular marker of DNA double-strand breaks , 2011, Genome Integrity.

[50]  P. Jeggo,et al.  The life and death of DNA-PK , 2005, Oncogene.

[51]  Christophe E. Redon,et al.  Characteristics of γ-H2AX foci at DNA double-strand breaks sites , 2003 .

[52]  M. Stuschke,et al.  Use of γH2AX and other biomarkers of double-strand breaks during radiotherapy. , 2010, Seminars in radiation oncology.

[53]  Michael Scholz,et al.  Modeling Cell Survival after Photon Irradiation Based on Double-Strand Break Clustering in Megabase Pair Chromatin Loops , 2012, Radiation research.

[54]  David J. Chen,et al.  Repair of HZE-Particle-Induced DNA Double-Strand Breaks in Normal Human Fibroblasts , 2008, Radiation research.

[55]  Qi Ding,et al.  Autophosphorylation-dependent remodeling of the DNA-dependent protein kinase catalytic subunit regulates ligation of DNA ends. , 2004, Nucleic acids research.

[56]  B. Salles,et al.  Ionizing-radiation induced DNA double-strand breaks: a direct and indirect lighting up. , 2013, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[57]  J. Cleaver,et al.  Phosphorylated H2Ax is not an unambiguous marker for DNA double-strand breaks , 2011, Cell cycle.

[58]  L. Wiesmüller,et al.  In vitro model for DNA double‐strand break repair analysis in breast cancer reveals cell type–specific associations with age and prognosis , 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[59]  S. Lees-Miller,et al.  The DNA-dependent protein kinase: A multifunctional protein kinase with roles in DNA double strand break repair and mitosis. , 2015, Progress in biophysics and molecular biology.