期刊
JOURNAL OF VIROLOGY
卷 79, 期 20, 页码 12961-12968出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.79.20.12961-12968.2005
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资金
- NIAID NIH HHS [AI13718, AI032957, R01 AI032957, R56 AI013718, R01 AI013718] Funding Source: Medline
The cytomegalovirus (CMV) maturational protease, assemblin, contains an internal (1) cleavage site absent from its homologs in other herpesviruses. Blocking this site for cleavage did not prevent replication of the resulting I- mutant virus. However, cells infected with the I- virus showed increased amounts of a fragment produced by cleavage at the nearby cryptic (C) site, suggesting that its replication may bypass the I-site block by using the C site as an alternate cleavage pathway. To test this and further examine the biological importance of these cleavages, we constructed two additional virus mutants-one blocked for C-site cleavage and another blocked for both I- and C-site cleavage. Infectivity comparisons with the parental wild-type virus showed that the I- mutant was the least affected for virus production, whereas infectivity of the C- mutant was reduced by approximate to 40% and when both sites were blocked virus infectivity was reduced by nearly 90%, providing the first evidence that these cleavages have biological significance. We also present and discuss evidence suggesting that I-site cleavage destabilizes assemblin and its fragments, whereas C-site cleavage does not.
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