ASSOCIATION OF HERPES-SIMPLEX VIRUS REGULATORY PROTEIN ICP22 WITH TRANSCRIPTIONAL COMPLEXES CONTAINING EAP, ICP4, RNA-POLYMERASE-II, AND VIRAL-DNA REQUIRES POSTTRANSLATIONAL MODIFICATION BY THE U(L)13 PROTEIN-KINASE
R. Leopardi et al., ASSOCIATION OF HERPES-SIMPLEX VIRUS REGULATORY PROTEIN ICP22 WITH TRANSCRIPTIONAL COMPLEXES CONTAINING EAP, ICP4, RNA-POLYMERASE-II, AND VIRAL-DNA REQUIRES POSTTRANSLATIONAL MODIFICATION BY THE U(L)13 PROTEIN-KINASE, Journal of virology, 71(2), 1997, pp. 1133-1139
The expression of herpes simplex virus 1 gamma (late) genes requires f
unctional alpha proteins (gamma(1) genes) and the onset of viral DNA s
ynthesis (gamma(2) genes), We report that late in infection after the
onset of viral DNA synthesis, cell nuclei exhibit defined structures w
hich contain two viral regulatory proteins (infected cell proteins 4 a
nd 22) required for gamma gene expression, RNA polymerase II, a host n
ucleolar protein (EAP or L22) known to be associated with ribosomes an
d to bind small RNAs, including the Epstein-Barr virus small nuclear R
NAs, and newly synthesized progeny DNA. The formation of these complex
es required the onset of viral DNA synthesis. The association of infec
ted cell protein 22, a highly posttranslationally processed protein, w
ith these structures did not occur in cells infected with a viral muta
nt deleted in the genes U(L)13 and U(S)3, each of which specifies a pr
otein kinase known to phosphorylate the protein.