Chromatin from EJ cells infected with 100 multiplicity of infection (MOI) of either AdM or AdnL or uninfected or treated with sCD40L for 20 min or 18 h was used for immunoprecipitation with an anti-c-Rel, anti-RNA polymerase II (Pol II) or rabbit isotype antibodies and precipitated DNA spanning the NORE1A promoter c-Rel-binding site was assessed by PCR. The gene discussed is REL; the disease is infection.