- Open Access
Human cytomegalovirus UL76 induces chromosome aberrations
© Siew et al; licensee BioMed Central Ltd. 2009
Received: 15 April 2009
Accepted: 25 November 2009
Published: 25 November 2009
Human cytomegalovirus (HCMV) is known to induce chromosome aberrations in infected cells, which can lead to congenital abnormalities in infected fetuses. HCMV UL76 belongs to a conserved protein family from herpesviruses. Some reported roles among UL76 family members include involvement in virulence determination, lytic replication, reactivation of latent virus, modulation of gene expression, induction of apoptosis, and perturbation of cell cycle progression, as well as potential nuclease activity. Previously, we have shown that stable expression of UL76 inhibits HCMV replication in glioblastoma cells.
To examine chromosomal integrity and the DNA damage signal γ-H2AX in cells constitutively expressing UL76, immunofluorescent cell staining and Western blotting were performed. The comet assay was employed to assess DNA breaks in cells transiently expressing UL76.
We report that stably transfected cells expressing UL76 developed chromosome aberrations including micronuclei and misaligned chromosomes, lagging and bridging. In mitotic cells expressing UL76, aberrant spindles were increased compared to control cells. However, cells with supernumerary centrosomes were marginally increased in UL76-expressing cells relative to control cells. We further demonstrated that UL76-expressing cells activated the DNA damage signal γ-H2AX and caused foci formation in nuclei. In addition, the number of cells with DNA breaks increased in proportion to UL76 protein levels.
Our findings suggest that the virus-associated protein UL76 induces DNA damage and the accumulation of chromosome aberrations.
Myriad chromosomal or genomic abnormalities are common in viral lytic and latent infected cells, and even in virus-associated tumors. Recent studies have consistently shown that cellular defense mechanisms recognize infections involving a wide range of DNA and RNA viruses as abnormally damaged DNA, including human immunodeficiency virus (HIV), Epstein-Barr virus (EBV), herpes simplex virus (HSV-1), adenovirus, and Simian virus 40 (SV40). DNA damage responses and repair pathways are thus activated after infection [1–5]. To counteract these intrinsic cellular defenses, the viruses have evolved strategies to mitigate DNA damage signal transduction, attenuate DNA repair pathways, and modulate cell cycle progression [6–11]. Overall, cells infected with virus accumulate DNA damage that is directly linked to viral pathogenicity and presumably leads to genomic instability.
HCMV is a ubiquitous pathogen in humans, and following primary infection sustains an asymptomatic latent infection. During life-long infection, the viral life cycle displays multiple phases within the human body. These include active lytic replication, a low level of persistent infection, and insidious latency. Notable clinical complications associated with HCMV infection are in utero congenital infection, opportunistic infection in immunocompromised patients, cardiovascular diseases, and possible malignant tumors [12–15].
Evidence indicates that HCMV causes chromosome aberrations following infection. These abnormalities include selective chromosome breakages, chromosome pulverization, premature chromatid condensation, and centrosome structural injury [16–19]. Specifically, UV-inactivated HCMV is capable of inducing site-specific breaks at positions 1q42 and 1q21 on chromosome 1 and centrosome injury, indicating that the damage is related to virion-associated proteins and unrelated to de novo viral protein production [16, 20, 21]. These specific DNA break-points may explain the congenital hearing loss of HCMV-infected neonates.
HCMV UL76 encodes a protein belonging to the conserved UL24 protein family from herpesviruses . Several lines of evidence have shown that the UL76 protein and its family members govern multiple functions. During a typical lytic replication cycle, UL76 transcripts are expressed with true-late kinetics . The UL76 protein predominantly localizes to the nucleus and nucleolus, resulting in a significant reduction in the number of promyelocytic leukemia (PML) bodies [24, 25], where HCMV gene expression and genome replication initiates . Functional analyses of HCMV coding contents were performed by Tn-mediated insertion, and a recombinant virus with an insertion in UL76 resulted in a significant reduction in virus production . Similarly, deletion of the entire UL76 ORF resulted in a total loss of virus production [28, 29]. We previously demonstrated that UL76 is able to regulate both repression and activation of gene expression . Particularly, UL76 is capable of repressing the expression of replication-essential genes in a dose-dependent manner, including UL54 (DNA polymerase), UL123 (major immediate-early gene) and UL112 (major early gene, pre-replication factor) . In addition, UL76 is involved in the late stage of egress, and it is present in three types of mature viral particles, the virion, NIEP, and DB . Virus-associated UL76 presumably plays a role in the modulation of gene expression once delivered into the cell at a very early stage of viral infection. This speculation is partly based upon the facts that there are significant decreases in protein production in UL76-expressing cells for IE (IE1p72 and IE2p82) proteins, early gene products UL44 (DNA polymerase processivity factor) and UL57 (single-stranded DNA binding protein), and the late gene encoding UL99 (tegument protein) . Consistent with the repression of gene expression, HCMV production is dramatically inhibited in UL76-expressing cells. In addition, in an HCMV genome-wide expression assay, UL76 is over-expressed in hematopoietic CD34+ cells latently infected with HCMV [30, 31]. Taken together, these results suggest that UL76 is not only an essential gene for lytic replication but also implicate UL76 in viral latency.
During the course of this study, Knizewski and colleagues proposed that the UL76 protein family contains a potential endonuclease motif (Pfam accession number: PF01646) using computational analysis . We show here that in UL76-expressing cell lines chromosome aberrations, micronuclei and chromosomal misalignments (laggings and bridgings) were significantly increased. Further, an increased number of these cells exhibited enhanced nuclear foci containing phosphorylated histone γ-H2AX. We also show that UL76 induces DNA breaks in proportion to its protein levels, and marginally subverts mitotic fidelity by inducing aberrant spindles and supernumerary centrosomes relative to control cells. Our results therefore suggest that HCMV UL76 may be a source of chromosomal abnormalities, and the fundamental alteration of the cellular biochemical environment may modulate viral production.
Human embryonic lung cells (HEL299, ATCC), COS-1 cells, and human glioblastoma U-373 MG cells were maintained in Eagle's MEM supplemented with 10% fetal bovine serum (FBS). Methods for the construction, selection and maintenance of G418-resistant cells expressing UL76 were published previously . Stably transfected cell lines expressing UL76 were designated S1, S3, S4, and S5, and the parallel control cell line stably transfected with the cloning vector pBK-CMV was designated P7. These stable cells were routinely maintained in the presence of 25 μg/ml G418 (Pierce Biotechnology Inc., Rockford, IL, USA).
Primary mouse monoclonal antibodies (mAbs) used in this study include anti-α-tubulin (clone B-5-1-2, Sigma-Aldrich, St. Louis, Mo, USA), anti-γ-tubulin (clone GTU-88, Sigma-Aldrich, St. Louis, MO, USA), anti-γ-H2AX (Ser139) (clone JBW301, Upstate Biotechnology, Charlottesville, VA, USA) and anti-myc (Invitrogen, Carlsbad, CA, USA).
Plasmid construction and transient protein expression
A 975-bp DNA fragment encompassing nucleotides 111 258 to 112 232 of HCMV AD169 (annotated genome accession number NC001347) encoding full-length UL76 was amplified by polymerase chain reaction using the 5' and 3' primers, GGATCC CACCATGCCGTCCGGGCGT and GAATTC CTAAAGACCGTGTGGGACGGCA, respectively. BamHI and EcoRI (in bold) sites were generated at the ends of each amplified DNA fragment. The cloning vector pEF1/Myc-His (Invitrogen, Carlsbad, CA, USA) and the amplified UL76 DNA were digested with BamHI and EcoRI and re-ligated. The resulting plasmid was designated pUL76-myc and encoded a myc epitope at the C terminus of UL76. Transient expression of UL76 was achieved by seeding 2 × 105 cells in a 6-well culture dish. Plasmid DNA was transfected with Lipofectamine Plus reagent (Invitrogen, Carlsbad, CA, USA). Total DNA for each transfection was maintained at a constant 1 μg per well by addition of the empty cloning vector pEF1/Myc-His where necessary.
Indirect immunofluorescent analyses
Detailed protocols for immunofluorescent cell staining have been described . In brief, stably transfected U-373 MG cells were seeded onto a coverslip (20 × 104 cells per well) in six-well culture plates one day before staining. The following day, the cells were fixed in 2% paraformaldehyde in phosphate-buffered saline (PBS) for 10 minutes at room temperature and then permeabilized with 1% Triton X-100 in PBS for 20 minutes at 65°C. To detect mitotic spindles, cells were stained with α-tubulin or γ-tubulin monoclonal antibodies at a dilution of 1: 500 and incubated for 30 minutes at 37°C in a humidity chamber. After extensive washing in PBS, the cells were immersed in a solution containing one μg/ml DAPI and the secondary antibody Texas Red-conjugated goat anti-mouse immunoglobulin G (1: 1000 dilution, Vector Laboratories, Burlingame, CA, USA) for 30 minutes at 37°C. Characteristics of chromosome aberrations including the presence of micronuclei, abnormal spindles, chromosomal misalignments, chromosomal laggings and mitotic bridgings were recorded. To assess the induction of the γ-H2AX protein and the formation of foci by HCMV UL76, the γ-H2AX foci were visualized by immunofluorescent staining. Asynchronous stably-transfected cells were cultured on coverslips and washed twice with PBS, fixed for 10 minutes with 1% paraformaldehyde in PBS, permeabilized with 0.1% NP-40 in PBS for 30 minutes on ice, and then incubated with γ-H2AX mAb (1:1000), followed by goat anti-mouse IgG secondary antibody conjugated to Alexa Flour® 488 (Molecular Probe, Eugene, OR, USA). Coverslips were air dried and preserved in Prolong® Gold anti-fade reagent (Molecular Probe, Eugene, OR, USA). Confocal images were acquired with a laser scanning confocal microscope (Olympus FV1000). Images were processed with Adobe Photoshop (version 9.0) software.
Western blot analyses
γ-H2AX (Ser139) was detected in cells following a protocol for acid extraction of protein. Asynchronous cells were cultured to 90% confluency in 10 cm dishes and harvested by centrifugation. Cell pellets were suspended in lysis buffer containing 10 mM HEPES, pH 7.9, 1.5 mM MgCl2, 10 mM KCl, 0.5 mM DTT, and 1.5 mM PMSF. HCl was added to a final concentration of 0.2 M and the acidified protein extracts were incubated for 30 minutes on ice. Acid soluble proteins were dialyzed in 0.1 M acetic acid with several changes of ddH2O. To examine the production of UL76 or α-tubulin by Western blotting, transfected cells were lysed in RIPA buffer (50 mM Tris pH 7.5, 150 mM NaCl, 1% NP-40, 0.05% sodium deoxycholate, and 0.01% SDS) containing complete protease inhibitor cocktail (Roche, Mannheim, Germany). Soluble proteins were collected and total protein was quantified using a Bio-Rad Bradford protein assay kit (Bio-Rad, Hercules, CA, USA). Thirty micrograms of protein were boiled for 5 minutes in 5% β-mercaptoethanol reducing Laemmli sample buffer, and proteins were separated by SDS-10% PAGE then transferred to PVDF membrane (Hybond-P, GE healthcare, Piscataway, NJ, USA) in a Towbin transfer buffer (48 mM Tris, 39 mM glycine [pH 9.2]). Membranes were blocked in Tris-buffered saline (TBS, 50 mM Tris, 150 mM NaCl [pH7.5]) containing 1% skim milk for one hour and then probed with the anti-myc or anti-α-tubulin antibody indicated in the text followed by a 1:30,000 dilution of horseradish peroxidase-conjugated anti-mouse immunoglobulin G (GE Healthcare, Piscataway, NJ, USA). Chemiluminescent signals were generated using Lumi-LightPlus Western blotting substrate (Roche, Mannheim, Germany) and recorded on Hyperfilm™ ECL (GE Healthcare, Piscataway, NJ, USA).
To assess induction of DNA breaks by HCMV UL76 in vivo, pUL76-myc was transiently expressed in HEL299 and COS-1 cells. One day post-transfection, DNA breaks were detected using the CometAssay kit (Trevigen, Gaithersburg, MD, USA). Cells were harvested and combined to a concentration of 1 × 105 cells/ml in molten low-melting agarose at a ratio of 1:10 to immobilize the cells onto the CometSlide. Following a gentle lysis in 1% sodium lauryl sarcosinate cells were treated with alkaline solution (0.3 M NaOH, 1 mM EDTA) for one hour in the dark to unwind, denature the DNA and hydrolyze the sites of damage. Cells were then subjected to alkaline electrophoresis at 1.0 volt cm-1 at 4°C for one hour. Slides were subsequently rinsed by dipping several times in ddH2O and then immersed for five minutes in 70% ethanol. Slides were allowed to air dry and cells were visualized by staining with SYBR Green and scored by epifluorescence microscopy for the distribution of DNA between the "tail" and the "head". At least 75 randomly selected cells were scored per sample.
Statistical significance was assessed using the chi-square two-tailed test for independent samples. At least three independent experiments were evaluated for each cell population and the mean ± standard deviation is given.
HCMV UL76-expressing cells induce micronuclei formation
UL76-expressing cells induce chromosomal misalignments during mitosis
UL76-expressing cells moderately enhance aberrations in mitotic spindles and centrosomes
In summary, our data suggest that chromosomal abnormalities, micronuclei, lagging and bridging are significantly induced in UL76-expressing cells. However, centrosome number and spindle network, two key structures that maintain the fidelity of progression through the mitotic phase, did not appear significantly affected. Based on these observations, we investigated whether the cell signals of DNA damage were induced normally.
The DNA damage signal γ-H2AX is activated in UL76-expressing cells
In vivo expression of UL76 stimulates cellular DNA breaks
The HCMV UL76 protein is a member of the highly conserved protein family including herpes simplex virus (HSV-1 and 2) UL24 and murine gammaherpesvirus 68 (MHV68) ORF20. To characterize the function of the UL76 protein family, the initial effort employed an animal model to evaluate infectivity of HSV-1 encoding a defective UL24, which suggested that viruses with mutations in UL24 show decreases in productive replication and reactivation efficiency of latent virus from ganglion . Consistent with these observations, mice and guinea pigs infected with HSV-2 containing the mutated UL24 exhibit less genital lesions compared to that of wild type virus . Both reports are consistent with the characteristics of HCMV UL76, which is involved in viral lytic production and in latency [27, 28, 30, 31].
Second, it is documented that (MHV68) ORF20, a homolog HCMV UL76, induces DNA damage, apoptosis and arrests the cell cycle at the G2/M phase as a result of inactivation of the kinase activity of the cyclin B/cdc2 complex [36, 37]. Finally, sequence analyses indicate the family members contain potential endonuclease PD-(D/E)XK motifs [32, 38]. This prediction is in agreement with previous speculation that the HCMV UL76 and UL77 proteins, homologs of HSV UL24 and UL25, respectively, may be involved in the final stages of genome cleavage and packaging [12, 39, 40].
In this report, we present evidence showing that stably transfected cells expressing UL76 accumulate multiple chromosome aberrations. Micronuclei (MN) were first noted in interphase in UL76-expressing cells (Fig. 1). Micronucleus formation is known to derive from incorrectly aligned chromosomes in metaphase (displaced chromosomes), as well as lagging and bridging chromosomes . Consistent with this result and the previous documentation, the ratios of chromosomal misalignments in UL76-expressing mitotic cells, both lagging and bridging, were statistically significant. However, these cells did not appear to trigger responses to DNA damage that are detrimental, suggesting that UL76 may be involved in the evasion of DNA damage responses, cell cycle checkpoint surveillance or inhibition of DNA repair machinery. We investigated signaling pathways that are responsive to DNA breaks in attempts to derive a mechanism for the observed responses. Immediately following DNA damage, histone H2AX is phosphorylated by phosphoinositide 3-kinase like kinases ATM, ATR, and DNA-PKs . Phosphorylated H2AX (γ-H2AX) is recruited to the broken DNA and are visible as foci in cell nuclei. The levels of γ-H2AX and percentage of foci increased in UL76-expressing cells, suggesting the signal for DNA damage is activated and functional. The induction of DNA breaks by UL76 was further evaluated by Comet assay. We observed that cells developed comet tails when UL76 was transiently expressed in both HCMV permissive HEL299 cells and in non-permissive COS-1 cells. This property is in contrast to the response elicited by HSV-1 infection, in which the induction of the DNA damage response occurs only within permissive cells . Moreover, the percentage of cells with comet tails increased as the levels of UL76 increased, suggesting that UL76 plays a role in DNA breakage. Induction of DNA damage may reflect potential activity of UL76 as an endonuclease .
In addition to the induction of DNA breaks many viral proteins also affect the spindle network or centrosome number in mitotic cells, which may lead to the emergence of aneuploidy cells [44, 45]. The correlation between extra centrosome number and aneuploidy is visibly observed by images that show that supernumerary centrosomes promote the emergence of lagging chromosomes during anaphase. In contrast, cells with supernumerary centrosomes undergoing multipolar cell divisions are almost non-viable . This report may explain the fact that cells with a multiple centrosome number were minimally detected in UL76-expressing cells.
In summary, our findings suggest that UL76 induces chromosome aberrations. Apparently, cells stably expressing UL76 are not capable of fully repairing the damage because we observed that micronuclei, chromosomal lagging and bridging accumulate in cells constitutively expressing UL76. It is of interest to explore the mechanisms involved in the emergence of chromosome aberrations, including endonuclease activity, evasion of the DNA damage response and mitigation of checkpoint surveillance exerted by HCMV UL76.
This study was supported by National Science Council research grants NSC94-2311-B-037-004, NSC95-2320-B-037-034, and NSC96-2320-B-037-007 awarded to S.-K. Wang.
- Kamranvar SA, Gruhne B, Szeles A, Masucci MG: Epstein-Barr virus promotes genomic instability in Burkitt's lymphoma. Oncogene. 2007, 26: 5115-5123. 10.1038/sj.onc.1210324.View ArticlePubMedGoogle Scholar
- Everett RD: Interactions between DNA viruses, ND10 and the DNA damage response. Cell Microbiol. 2006, 8: 365-374. 10.1111/j.1462-5822.2005.00677.x.View ArticlePubMedGoogle Scholar
- Lilley CE, Schwartz RA, Weitzman MD: Using or abusing: viruses and the cellular DNA damage response. Trends Microbiol. 2007, 15: 119-126. 10.1016/j.tim.2007.01.003.View ArticlePubMedGoogle Scholar
- Sinclair A, Yarranton S, Schelcher C: DNA-damage response pathways triggered by viral replication. Expert Rev Mol Med. 2006, 8: 1-11. 10.1017/S1462399406010544.PubMed CentralView ArticlePubMedGoogle Scholar
- Weitzman MD, Carson CT, Schwartz RA, Lilley CE: Interactions of viruses with the cellular DNA repair machinery. DNA repair. 2004, 3: 1165-1173. 10.1016/j.dnarep.2004.03.018.View ArticlePubMedGoogle Scholar
- Luo MH, Rosenke K, Czornak K, Fortunato EA: Human cytomegalovirus disrupts both ataxia telangiectasia mutated protein (ATM)- and ATM-Rad3-related kinase-mediated DNA damage responses during lytic infection. J Virol. 2007, 81: 1934-1950. 10.1128/JVI.01670-06.PubMed CentralView ArticlePubMedGoogle Scholar
- Hrecka K, Gierszewska M, Srivastava S, Kozaczkiewicz L, Swanson SK, Florens L, Washburn MP, Skowronski J: Lentiviral Vpr usurps Cul4-DDB1[VprBP] E3 ubiquitin ligase to modulate cell cycle. Proc Natl Acad Sci USA. 2007, 104: 11778-11783. 10.1073/pnas.0702102104.PubMed CentralView ArticlePubMedGoogle Scholar
- Schrofelbauer B, Hakata Y, Landau NR: HIV-1 Vpr function is mediated by interaction with the damage-specific DNA-binding protein DDB1. Proc Natl Acad Sci USA. 2007, 104: 4130-4135. 10.1073/pnas.0610167104.PubMed CentralView ArticlePubMedGoogle Scholar
- Nguyen ML, Blaho JA: Apoptosis during herpes simplex virus infection. Adv Virus Res. 2007, 69: 67-97. 10.1016/S0065-3527(06)69002-7.View ArticlePubMedGoogle Scholar
- Wilkinson DE, Weller SK: Herpes simplex virus type I disrupts the ATR-dependent DNA-damage response during lytic infection. J Cell Sci. 2006, 119: 2695-2703. 10.1242/jcs.02981.PubMed CentralView ArticlePubMedGoogle Scholar
- Marriott SJ, Semmes OJ: Impact of HTLV-I Tax on cell cycle progression and the cellular DNA damage repair response. Oncogene. 2005, 24: 5986-5995. 10.1038/sj.onc.1208976.View ArticlePubMedGoogle Scholar
- Mocarski ES, Shenk T, Pass RF: Cytomegalovirus. Field's Virology. Edited by: Knight DM, Howley PM. 2007, Philadelphia: Lippincott Williams & Wilkins, 2701-2772. 5Google Scholar
- Reddehase MJ: Cytomegaloviruses Molecular Biology and Immunology. 2006, Norfolk, UK; Caister Academic PressGoogle Scholar
- Cheng J, Ke Q, Jin Z, Wang H, Kocher O, Morgan JP, Zhang J, Crumpacker CS: Cytomegalovirus infection causes an increase of arterial blood pressure. PLoS Pathog. 2009, 5: e1000427-10.1371/journal.ppat.1000427.PubMed CentralView ArticlePubMedGoogle Scholar
- Reeves M, Sinclair J: Aspects of human cytomegalovirus latency and reactivation. Curr Top Microbiol Immunol. 2008, 325: 297-313. full_text.PubMedGoogle Scholar
- Fortunato EA, Spector DH: Viral induction of site-specific chromosome damage. Rev Med Virol. 2003, 13: 21-37. 10.1002/rmv.368.View ArticlePubMedGoogle Scholar
- Luleci G, Sakizli M, Gunalp A: Selective chromosomal damage caused by human cytomegalovirus. Acta Virol. 1980, 24: 341-345.PubMedGoogle Scholar
- AbuBakar S, Au WW, Legator MS, Albrecht T: Induction of chromosome aberrations and mitotic arrest by cytomegalovirus in human cells. Environ Mol Mutagen. 1988, 12: 409-420.View ArticlePubMedGoogle Scholar
- Bystrevskaya VB, Lobova TV, Smirnov VN, Makarova NE, Kushch AA: Centrosome injury in cells infected with human cytomegalovirus. J Struct Biol. 1997, 120: 52-60. 10.1006/jsbi.1997.3897.View ArticlePubMedGoogle Scholar
- Nystad M, Fagerheim T, Brox V, Fortunato EA, Nilssen O: Human cytomegalovirus (HCMV) and hearing impairment: Infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49-Both involved in dominantly inherited, sensorineural, hearing impairment. Mutat Res. 2008, 637: 56-65.PubMed CentralView ArticlePubMedGoogle Scholar
- Fortunato EA, Dell'Aquila ML, Spector DH: Specific chromosome 1 breaks induced by human cytomegalovirus. Proc Natl Acad Sci USA. 2000, 97: 853-858. 10.1073/pnas.97.2.853.PubMed CentralView ArticlePubMedGoogle Scholar
- Dezelee S, Bras F, Vende P, Simonet B, Nguyen X, Flamand A, Masse MJ: The BamHI fragment 9 of pseudorabies virus contains genes homologous to the UL24, UL25, UL26, and UL 26.5 genes of herpes simplex virus type 1. Virus Res. 1996, 42: 27-39. 10.1016/0168-1702(96)01293-2.View ArticlePubMedGoogle Scholar
- Wang S-K, Duh C-Y, Wu C-W: Human cytomegalovirus UL76 encodes a novel virion-associated protein that is able to inhibit viral replication. J Virol. 2004, 78: 9750-9762. 10.1128/JVI.78.18.9750-9762.2004.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang S-K, Duh C-Y, Chang T-T: Cloning and identification of regulatory gene UL76 of human cytomegalovirus. J Gen Virol. 2000, 81: 2407-2416.View ArticlePubMedGoogle Scholar
- Salsman J, Zimmerman N, Chen T, Domagala M, Frappier L: Genome-wide screen of three herpesviruses for protein subcellular localization and alteration of PML nuclear bodies. PLoS Pathog. 2008, 4: e1000100-10.1371/journal.ppat.1000100.PubMed CentralView ArticlePubMedGoogle Scholar
- Ishov AM, Stenberg RM, Maul GG: Human cytomegalovirus immediate early interaction with host nuclear structures: definition of an immediate transcript environment. J Cell Biol. 1997, 138: 5-16. 10.1083/jcb.138.1.5.PubMed CentralView ArticlePubMedGoogle Scholar
- Yu D, Silva MC, Shenk T: Functional map of human cytomegalovirus AD169 defined by global mutational analysis. Proc Natl Acad Sci USA. 2003, 100: 12396-12401. 10.1073/pnas.1635160100.PubMed CentralView ArticlePubMedGoogle Scholar
- Dunn W, Chou C, Li H, Hai R, Patterson D, Stolc V, Zhu H, Liu F: Functional profiling of a human cytomegalovirus genome. Proc Natl Acad Sci USA. 2003, 100: 14223-14228. 10.1073/pnas.2334032100.PubMed CentralView ArticlePubMedGoogle Scholar
- Murphy E, Shenk T: Human cytomegalovirus genome. Curr Top Microbiol Immunol. 2008, 325: 1-19. full_text.PubMedGoogle Scholar
- Goodrum F, Jordan CT, Terhune SS, High K, Shenk T: Differential outcomes of human cytomegalovirus infection in primitive hematopoietic cell subpopulations. Blood. 2004, 104: 687-695. 10.1182/blood-2003-12-4344.View ArticlePubMedGoogle Scholar
- Goodrum FD, Jordan CT, High K, Shenk T: Human cytomegalovirus gene expression during infection of primary hematopoietic progenitor cells: a model for latency. Proc Natl Acad Sci USA. 2002, 99: 16255-16260. 10.1073/pnas.252630899.PubMed CentralView ArticlePubMedGoogle Scholar
- Knizewski L, Kinch L, Grishin NV, Rychlewski L, Ginalski K: Human herpesvirus 1 UL24 gene encodes a potential PD-(D/E)XK endonuclease. J Virol. 2006, 80: 2575-2577. 10.1128/JVI.80.5.2575-2577.2006.PubMed CentralView ArticlePubMedGoogle Scholar
- Paull TT, Rogakou EP, Yamazaki V, Kirchgessner CU, Gellert M, Bonner WM: A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage. Curr Biol. 2000, 10: 886-895. 10.1016/S0960-9822(00)00610-2.View ArticlePubMedGoogle Scholar
- Jacobson JG, Chen SH, Cook WJ, Kramer MF, Coen DM: Importance of the herpes simplex virus UL24 gene for productive ganglionic infection in mice. Virology. 1998, 242: 161-169. 10.1006/viro.1997.9012.View ArticlePubMedGoogle Scholar
- Blakeney S, Kowalski J, Tummolo D, DeStefano J, Cooper D, Guo M, Gangolli S, Long D, Zamb T, Natuk RJ, Visalli RJ: Herpes simplex virus type 2 UL24 gene is a virulence determinant in murine and guinea pig disease models. J Virol. 2005, 79: 10498-10506. 10.1128/JVI.79.16.10498-10506.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Nascimento R, Parkhouse RM: Murine gammaherpesvirus 68 ORF20 induces cell-cycle arrest in G2 by inhibiting the Cdc2-cyclin B complex. J Gen Virol. 2007, 88: 1446-1453. 10.1099/vir.0.82589-0.View ArticlePubMedGoogle Scholar
- Nascimento R, Dias JD, Parkhouse RM: The conserved UL24 family of human alpha, beta and gamma herpesviruses induces cell cycle arrest and inactivation of the cyclinB/cdc2 complex. Arch Virol. 2009, 154: 1143-1149. 10.1007/s00705-009-0420-y.View ArticlePubMedGoogle Scholar
- Kosinski J, Feder M, Bujnicki JM: The PD-(D/E)XK superfamily revisited: identification of new members among proteins involved in DNA metabolism and functional predictions for domains of (hitherto) unknown function. BMC bioinformatics. 2005, 6: 172-184. 10.1186/1471-2105-6-172.PubMed CentralView ArticlePubMedGoogle Scholar
- Stow ND: Packaging of genomic and amplicon DNA by the herpes simplex virus type 1 UL25-null mutant KUL25NS. J Virol. 2001, 75: 10755-10765. 10.1128/JVI.75.22.10755-10765.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Bowman BR, Welschhans RL, Jayaram H, Stow ND, Preston VG, Quiocho FA: Structural characterization of the UL25 DNA-packaging protein from herpes simplex virus type 1. J Virol. 2006, 80: 2309-2317. 10.1128/JVI.80.5.2309-2317.2006.PubMed CentralView ArticlePubMedGoogle Scholar
- Rao X, Zhang Y, Yi Q, Hou H, Xu B, Chu L, Huang Y, Zhang W, Fenech M, Shi Q: Multiple origins of spontaneously arising micronuclei in HeLa cells: direct evidence from long-term live cell imaging. Mutat Res. 2008, 646: 41-49.View ArticlePubMedGoogle Scholar
- Stucki M, Jackson SP: gammaH2AX and MDC1: anchoring the DNA-damage-response machinery to broken chromosomes. DNA repair. 2006, 5: 534-543. 10.1016/j.dnarep.2006.01.012.View ArticlePubMedGoogle Scholar
- Lilley CE, Carson CT, Muotri AR, Gage FH, Weitzman MD: DNA repair proteins affect the lifecycle of herpes simplex virus 1. Proc Natl Acad Sci USA. 2005, 102: 5844-5849. 10.1073/pnas.0501916102.PubMed CentralView ArticlePubMedGoogle Scholar
- Kops GJ, Weaver BA, Cleveland DW: On the road to cancer: aneuploidy and the mitotic checkpoint. Nat Rev Cancer. 2005, 5: 773-785. 10.1038/nrc1714.View ArticlePubMedGoogle Scholar
- Rajagopalan H, Lengauer C: Aneuploidy and cancer. Nature. 2004, 432: 338-341. 10.1038/nature03099.View ArticlePubMedGoogle Scholar
- Ganem NJ, Godinho SA, Pellman D: A mechanism linking extra centrosomes to chromosomal instability. Nature. 2009, 460: 278-282. 10.1038/nature08136.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.