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Analysis of in vitro transcription products of intracellular vesicular stomatitis virus RNA polymerase.

作者信息

Galet H, Hallett D, Prevec L

出版信息

J Virol. 1976 Aug;19(2):467-74. doi: 10.1128/JVI.19.2.467-474.1976.

Abstract

The intracellular transcriptase complex of vesicular stomatitis virus-infected L cells synthesized RNA complementary to the entire infectious virus genome at either 37 degrees C or 28 degrees C in vitro. Not all sequences were present at the same frequency, however; copies of that segment of the genome common to the LT defective particles were present at 20 to 100 times higher frequently than copies of the genome segment common to the ST defective particle. The less frequent region was transcribed somewhat more effectively at 28 degrees C than at 37 degrees C. The results suggest that transcriptional regulation rather than selective degradation is responsible for the differential accumulation of RNA.

摘要

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引用本文的文献

1
In vitro synthesis of a unique RNA species by a T particle of vesicular stomatitis virus.
J Virol. 1977 Sep;23(3):708-16. doi: 10.1128/JVI.23.3.708-716.1977.

本文引用的文献

1
Analysis of the RNA of defective VSV particles.
Cell. 1974 Sep;3(1):85-93. doi: 10.1016/0092-8674(74)90044-0.
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The RNA of defective vesicular stomatitis virus particles in relation to viral cistrons.
J Mol Biol. 1974 Jan 5;85(4):551-68. doi: 10.1016/0022-2836(74)90315-5.
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In vitro synthesis of RNA that contains polyadenylate by virion-associated RNA polymerase of vesicular stomatitis virus.
Proc Natl Acad Sci U S A. 1973 Dec;70(12):3566-70. doi: 10.1073/pnas.70.12.3566.
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Polyadenylate synthesis by extracts from L cells infected with vesicular stomatitis virus.
Nat New Biol. 1973 Jun 13;243(128):200-3. doi: 10.1038/newbio243200a0.
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J Mol Biol. 1971 Jun 28;58(3):799-814. doi: 10.1016/0022-2836(71)90041-6.
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