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Carcinogen-induced accumulation of adeno-associated parvovirus dna is transient as a result of two antagonistic activities that both require De Novo protein synthesis

✍ Scribed by Ursula Bantel-Schaal


Book ID
102866750
Publisher
John Wiley and Sons
Year
1993
Tongue
French
Weight
656 KB
Volume
53
Category
Article
ISSN
0020-7136

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✦ Synopsis


Abstract

Helper‐independent synthesis of adeno‐associated parvovirus type 5 (AAV‐5) DNA in SV40‐transformed Syrian hamster cells is induced by chemical carcinogens, UV light and other stress treatments and has previously been shown to be transient. To gain some insight into the underlying mechanism, the influence of inhibitors of protein synthesis on AAV DNA accumulation was investigated. It is shown that transience is the result of 2 antagonistic activities‐synthesis and decomposition. Both depend on de novo protein synthesis and are in part overlapping. The 2 activities are influenced by the amount of AAV uptake and/or by cell density. In less dense cultures, calculated initial amount of AAV DNA and relative accumulation per cell are higher. The effect may be due to the activity of transiently synthesized AAV‐encoded regulatory proteins that increase replication and have inhibitory effects on DNA decomposition, or to the influence on cellular adhesion.