Use of differential display analysis to assess the effect of human cytomegalovirus infection on the accumulation of cellular RNAs: induction of interferon-responsive …

H Zhu, JP Cong, T Shenk - Proceedings of the National …, 1997 - National Acad Sciences
H Zhu, JP Cong, T Shenk
Proceedings of the National Academy of Sciences, 1997National Acad Sciences
We used differential display analysis to identify mRNAs that accumulate to enhanced levels
in human cytomegalovirus-infected cells as compared with mock-infected cells. RNAs were
compared at 8 hr after infection of primary human fibroblasts. Fifty-seven partial cDNA
clones were isolated, representing about 26 differentially expressed mRNAs. Eleven of the
mRNAs were virus-coded, and 15 were of cellular origin. Six of the partial cDNA sequences
have not been reported previously. All of the cellular mRNAs identified in the screen are …
We used differential display analysis to identify mRNAs that accumulate to enhanced levels in human cytomegalovirus-infected cells as compared with mock-infected cells. RNAs were compared at 8 hr after infection of primary human fibroblasts. Fifty-seven partial cDNA clones were isolated, representing about 26 differentially expressed mRNAs. Eleven of the mRNAs were virus-coded, and 15 were of cellular origin. Six of the partial cDNA sequences have not been reported previously. All of the cellular mRNAs identified in the screen are induced by interferon α. The induction in virus-infected cells, however, does not involve the action of interferon or other small signaling molecules. Neutralizing antibodies that block virus infection also block the induction. These RNAs accumulate after infection with virus that has been inactivated by treatment with UV light, indicating that the inducer is present in virions. We conclude that human cytomegalovirus induces interferon-responsive mRNAs.
National Acad Sciences