MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair - PubMed (original) (raw)

. 2010 Jul;30(14):3582-95.

doi: 10.1128/MCB.01476-09. Epub 2010 May 17.

Sairei So, Arun Gupta, Rakesh Kumar, Christelle Cayrou, Nikita Avvakumov, Utpal Bhadra, Raj K Pandita, Matthew H Porteus, David J Chen, Jacques Cote, Tej K Pandita

Affiliations

MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair

Girdhar G Sharma et al. Mol Cell Biol. 2010 Jul.

Abstract

The human MOF gene encodes a protein that specifically acetylates histone H4 at lysine 16 (H4K16ac). Here we show that reduced levels of H4K16ac correlate with a defective DNA damage response (DDR) and double-strand break (DSB) repair to ionizing radiation (IR). The defect, however, is not due to altered expression of proteins involved in DDR. Abrogation of IR-induced DDR by MOF depletion is inhibited by blocking H4K16ac deacetylation. MOF was found to be associated with the DNA-dependent protein kinase catalytic subunit (DNA-PKcs), a protein involved in nonhomologous end-joining (NHEJ) repair. ATM-dependent IR-induced phosphorylation of DNA-PKcs was also abrogated in MOF-depleted cells. Our data indicate that MOF depletion greatly decreased DNA double-strand break repair by both NHEJ and homologous recombination (HR). In addition, MOF activity was associated with general chromatin upon DNA damage and colocalized with the synaptonemal complex in male meiocytes. We propose that MOF, through H4K16ac (histone code), has a critical role at multiple stages in the cellular DNA damage response and DSB repair.

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Figures

FIG. 1.

FIG. 1.

Correlation between status of H4K16ac levels and IR-induced γ-H2AX focus formation in 293 cells. (A) Simultaneous detection of cells transfected with Cy3-labeled siRNA, H4K16ac status, and γ-H2AX focus appearance after exposure to 1.5 Gy of IR. (Aa and Ab) Cells were transfected with hMOF siRNA and analyzed for γ-H2AX foci after 5 min (Aa) and 300 min (Ab) of IR exposure. (Ac and Ad) Cells were transfected with Tip60 siRNA and analyzed for γ-H2AX foci after 5 min (Ac) and 300 min (Ad) of IR exposure. Panels Aa and Ac are magnified cells as shown in Fig. S2A and B in the supplemental material. (B) Frequency of cells with more than 2 γ-H2AX foci observed at various time points postirradiation. For each time point, 100 cells were analyzed. Each experiment was repeated three times; the mean numbers of cells with more than 2 foci are plotted against time. (a) Appearance of γ-H2AX foci in cells with and without depletion of either hMOF or Tip60. (b) Disappearance of γ-H2AX foci in cells with and without depletion of either hMOF or Tip60.

FIG. 2.

FIG. 2.

Effect of H4K16ac levels on the appearance of IR-induced γ-H2AX foci. (A) 293 cells with and without knockdown of MOF were treated with TSA and examined for H4K16ac levels. Lane C, control. (B) Cells knocked down for hMOF and treated with TSA were irradiated and examined for appearance of γ-H2AX foci. (C) SirT2+/+ and SirT2−/− mouse embryonic fibroblasts with knockdown of MOF, showing MOF and H4K16ac levels and (D) frequency of IR-induced γ-H2AX foci cells. (E) HL60 cells treated with DMSO for different time periods showing MOF, H4K16ac, and histone H4. (F) HL60 cells treated with DMSO or MOF knockdown and irradiated with 1.5 Gy, showing frequency of cells with γ-H2AX postirradiation.

FIG. 3.

FIG. 3.

hMOF depletion influences IR-induced repair focus-associated proteins and hMOF interaction with chromatin. 293 cells with and without depletion of hMOF with reduced levels of H4K16ac were irradiated with 6 Gy and quantified for foci at different time points postirradiation. (A) For MDC1, cells with more than 5 foci were counted. (B) For 53BP1, cells with more than 3 foci were counted. (C) For induction of hSSB1 foci, cells were irradiated with 2 Gy and cells with more than 2 foci were counted after 1 h postirradiation. (D) RFP-Rad52-expressing 293 cells knocked down for MOF were grown in the presence of bromodeoxyuridine (BrdU) and incubated in Hoechst 33342. Subnuclear DNA damage was induced in the designated rectangular boxes using a 405-nm laser on an LSM510 Zeiss confocal live-imaging system. (E) Association of hMOF with chromatin was determined by ChIP analysis. Cells were irradiated with 5 Gy and fixed, chromatin immunoprecipitation was performed with an hMOF or Rb antibody, and DNA was quantified by absorbance at 260 nm by NanoDrop 2000. (F) Cells with and without exposure to IR were analyzed for the retention of hMOF by Western blotting. hMOF was detected with a specific hMOF antibody.

FIG. 4.

FIG. 4.

MOF depletion results in delayed appearance of γ-H2AX focus at a site-specific DNA DSB. (A) Mouse NIH2/4 cells with and without treatment with TA were fixed and examined for the presence of a γ-H2AX focus. The fluorescence of γ-H2AX, MOF, and DNA was measured across the nucleus and plotted on the top of the cell nucleus. Immunofluorescence was performed with anti-γ-H2AX, anti-H4K16ac, and anti-MOF antibody, and cells were counterstained with DAPI. Fluorescent intensities were measured using Isis or Zen software for each channel. (B) Western blot detection of MOF 72 h posttransfection with siRNA in NIH2/4 cells. (C) NIH2/4 cells with and without MOF depletion were treated with TA and fixed at different time points to detect a γ-H2AX focus by immunostaining. (D) ChIP analysis in I-SceI-induced cells with and without knockdown of MOF examined for bound MOF, H4K16ac, and histone H4. No changes of MOF and H4K16ac levels at the site of damage were detected. (E and F) Effect of MOF on NHEJ. (E) 293 engineered cell line that can become fluorescent (RFP) only upon repair of I-SceI-induced DSBs by NHEJ. CMV, cytomegalovirus; CBA, chicken β-actin promoter. (F) Depletion of MOF results decreased frequency of cells with RFP. These data clearly indicate that the cell's H4K16ac status plays a critical role in the NHEJ pathway.

FIG. 5.

FIG. 5.

Interaction of hMOF with DNA-PKcs. (A) hMOF-TAP is purified with distinct sets of associated proteins. The calmodulin fraction of hMOF-TAP was separated by SDS-PAGE and stained with Sypro Ruby Red, and gel slices were subjected to in-gel digestion and mass spectrometry. M, molecular mass marker. Peptides corresponding to hMSLs and other proteins were identified (numbers of peptides are shown in parentheses) (see Fig. S9 in the supplemental material). DNA-PKcs copurifies preferentially with hMOF. hMOF TAP-, hMSL3L1 TAP-, and mock TAP-purified fractions were assayed for the presence of hMSL1, HCF-1, and DNA-PKcs by Western blotting (B). (C) Cells with and without depletion of hMOF or Tip60 were irradiated with 5 Gy and examined for DNA-PKcs phosphorylation using antibodies specific for pS2056 and pT2609. Depletion of hMOF resulted in loss of ATM-dependent phosphorylation of DNA-PKcs (pT2609), and no such loss was observed in Tip60-depleted cells. (D) Recruitment of DNA-PKcs to the laser-induced DNA DSBs. Cells were transfected with YFP-DNA-PKcs and microirradiated. Time-lapse imaging of YFP-DNA-PKcs-expressing U2OS cells was done before and after microirradiation. (E) Cells stably expressing YFP-DNA-PKcs were treated with control or hMOF siRNA for 72 h, and microirradiated. (F) Initial accumulation kinetics (see Fig. S9B in the supplemental material) and relative fluorescence for a 2-h time course of treatment with YFP-DNA-PKcs at laser-generated DSBs. Error bars represent the standard deviations (SD) from three different experiments.

FIG. 6.

FIG. 6.

MOF plays a role in HR. (A) Cells with and without MOF or Tip60 knockdown were irradiated with different doses, and cells were quantified for the presence of Rad51 foci after 4 h of irradiation. (B) Impairment of I-SceI-induced HR in hMOF-deficient cells was found. HR frequencies are shown with (+) or without (−) I-SceI induction in untreated cells, in cells treated with control siRNA, and in cells treated with hMOF- or BRCA1-specific siRNA (54). The results presented are the mean and standard error from three independent experiments. (C) Localization of MOF on mouse meiotic chromosomes during prophase 1. Spermatocyte spreads from male mice were immunostained with anti-MOF, anti-TRF1, and anti-SCP. MOF is in red, synaptonemal complex protein SCP3 is green, and TRF1 is white on chromosomes from mouse spermatocytes. The presence of MOF on synaptonemal complexes from leptotene to mid-pachytene suggests the role of MOF in meiotic recombination.

FIG. 7.

FIG. 7.

MOF and H4K16ac influence DDR at multiple stages of DNA DSB repair pathways. MOF is a major HAT for H4K16ac, and its levels determine IR-induced repairosome formation. MOF interacts with DNA-PKcs and also localizes on the synaptonemal complex (SCP3) of meiocytes, thus linking to both the DNA DSB repair pathways.

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