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Enhanced capacity of DNA repair in human cytomegalovirus-infected cells.

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Figure

FIG.treatment
FIG. 2.[3H]thymidine.48mMlabeled h CsCl density gradient DNA analysis of HCMV-infected Vero cells labeled with BUdR and Confluent monolayers of Vero cells were infected with HCMV at a multiplicity of3 PFU/cell; later the cells were labeled with BUdR and ['Hithymidine for 2 h in the absence (a) orpresence (b) of20 of hydroxyurea or irradiated with UV light (c) at a dose of 20f) ergs per mm2 before labeling; 0, 14C- cellular DNA of normal density used as a marker; 0, DNA from HCMV-infected cells; \, buoyantdensity.
FIG. 3.perpresence,uCiHCMV-infectedthecells;treatmentirradiated Hydroxyurea-resistant DNA synthesis of or mock-infected Vero cells after with UV light (a) or MMS (b)
FIG. 4.[14C]thymidineU,aatVero dose UV-irradiated 10,500 Alkaline sucrose gradientprofiles ofnewly synthesized DNA from HCMV-infected or mock-infected cells irradiated with UV light
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