Figure 2From: UL28 and UL33 homologs of Marek’s disease virus terminase complex involved in the regulation of cleavage and packaging of viral DNA are indispensable for replication in cultured cellsConstruction and Identification of the UL28 and UL33 gene deletion and revertant constructs. A Schematic diagram represents a linear MDV genome consisting of a unique long (UL) region and a unique short (US) region. Both terminal repeats (TRL/TRS) and the internal repeat (IRL/IRS) regions locate on both sides of the UL and US region. Location of the UL28 and UL33 genes on MDV is also shown; B PCR analysis of the virus genome with UL28 and meq specific primers. The lanes 1, 2 and 3 indicate the PCR amplification of the UL28 gene using parental virus, MDV △UL28 or MDV △UL28-Re mutants as templates, respectively; The lanes 4, 5 and 6 indicate the PCR amplification of the Meq gene using parental virus, MDV △UL28 or MDV △UL28-Re mutants as templates, respectively; C PCR analysis of the virus genome with the UL33 and meq specific primers. The lanes 1, 2 and 3 indicate the PCR amplification of the UL28 gene using parental virus, MDV △UL33 or MDV △UL33-Re mutants as templates, respectively; the lanes 4, 5 and 6 indicate the PCR amplification of the Meq gene using parental virus, MDV △UL33 or MDV △UL33-Re mutants as templates, respectively; D RFLP analysis of the genomic DNAs of the parental virus, MDV △UL28 or MDV △UL28-Re. DNA was digested with EcoRV. lane 1 indicates the parental virus; lane 2 represents MDV △UL28; lane 3 indicates MDV △UL28-Re; E RFLP analysis of the genomic DNAs of the parental virus, MDV △UL33 or MDV △UL33-Re. DNA was digested with NdeI. lane 1 indicates the parental virus; lane 2 represents MDV △UL33; lane 3 indicates MDV △UL33-Re. The red arrow indicates the fragment size difference.Back to article page