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Titlebook: Viral Messenger RNA; Transcription, Proce Yechiel Becker,Julia Hadar (Managing Editor) Book 1985 Martinus Nijhoff Publishing, Boston 1985 c

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书目名称Viral Messenger RNA
副标题Transcription, Proce
编辑Yechiel Becker,Julia Hadar (Managing Editor)
视频video
丛书名称Developments in Molecular Virology
图书封面Titlebook: Viral Messenger RNA; Transcription, Proce Yechiel Becker,Julia Hadar (Managing Editor) Book 1985 Martinus Nijhoff Publishing, Boston 1985 c
描述The nucleotide sequence of the gene from which messenger RNA mole­ cules are transcribed is in a form that can be translated by cellular ribosomes into the amino acid sequence of a particular polypeptide, the product of the gene. The discovery of messenger RNA more than twenty years ago led to a series of studies on its organization and function in cells in the presence of infecting viruses. This volume is devoted to current studies in the field of cellular and viral messenger RNA. The studies presented provide an insight into molecular and genetic aspects of messenger RNA. Special attention was paid by the authors to the molecular organization of mRNA species, to the processing of mRNA molecules, and to the different strategies employed by DNA and RNA viruses in the synthesis of their mRNA. The ability of a virus to take over the protein-synthesizing mechanisms of an infected cell depends on its ability to produce mRNA molecules which can affect the host mRNA or utilize cellular components more efficiently. The differences between, and similarities of, the strategies of mRNA synthesis devised by various DNA and RNA viruses are described herein. This book should be of interest to a
出版日期Book 1985
关键词cell; gene; infection; virus
版次1
doihttps://doi.org/10.1007/978-1-4613-2585-7
isbn_softcover978-1-4612-9621-8
isbn_ebook978-1-4613-2585-7
copyrightMartinus Nijhoff Publishing, Boston 1985
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Herpesvirus mRNAation they encode. We have shown that, despite the appearance of a complex transcription map, generally each viral transcript encodes a specific polypeptide. Thus, high resolution transcription mapping leads to a high resolution genetic map of the virus. Further, the very large number of individuall
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Use of Cloned Epstein-Barr Virus DNA to Identify Genes that Determine the Fate of Viral Infection may be responsible for determining the fate of an EBV infection. Transcriptionally active regions of the genome were detected by hybridization of .P-labeled cDNA (reverse-transcribed from infected-cell RNA) to the different cloned Bam Hl restriction endonuclease fragments of EBV DNA. Analysis of th
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Reovirus mRNA and readily manipulated system for examining the nature of RNA-protein and RNA-RNA interactions, including the nature of the mechanisms that cause mRNAs to become incorporated into progeny virus particles, and the factors that regulate the efficiency with which they are translated.
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