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Basic Characteristics of Mutations
|
|
Mutation Site
|
W439R |
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Mutation Site Sentence
|
Under the assay conditions, the HPV 16 E1 mutant (W439R, G482D) did not support HPV origin-driven DNA synthesis. |
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Mutation Level
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Amino acid level |
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Mutation Type
|
Nonsynonymous substitution |
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Gene/Protein/Region
|
E1 |
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Standardized Encoding Gene
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E1
|
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Genotype/Subtype
|
HPV16 |
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Viral Reference
|
-
|
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Functional Impact and Mechanisms
|
|
Disease
|
-
|
|
Immune
|
- |
|
Target Gene
|
-
|
|
Clinical and Epidemiological Correlations
|
|
Clinical Information
|
- |
|
Treatment
|
- |
|
Location
|
- |
|
Literature Information
|
|
PMID
|
12565157
|
|
Title
|
DNA replicative functions of highly-expressed, codon-optimized human papillomavirus proteins E1 and E2
|
|
Author
|
Wang XM,Jansen KU,McClements WL
|
|
Journal
|
Journal of virological methods
|
|
Journal Info
|
2003 Mar;108(1):83-90
|
|
Abstract
|
Human papillomavirus (HPV) DNA replication requires functional HPV early (E) proteins E1 and E2. To determine the biological activity of HPV 16 E1 and E2 mutant proteins under consideration as vaccine candidates, we developed a sensitive real time PCR assay that monitors HPV origin-of-replication-driven DNA synthesis. The assay was used to determine the DNA replicative functions of highly-expressed, codon-optimized HPV 16 E1 and E2 wild type and mutant proteins in transient transfections. Under the assay conditions, the HPV 16 E1 mutant (W439R, G482D) did not support HPV origin-driven DNA synthesis. In contrast, however, an HPV 16 E2 mutant bearing an E39A substitution, reported previously to be severely compromised for DNA replication, was found to be reduced only two-fold in activity and, therefore, considered not sufficiently inactivated for use in vaccines that depend on endogenous protein expression.
|
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Sequence Data
|
-
|