HSV Mutagenesis

  • Robert S. Coffin
Part of the Methods in Molecular Medicine book series (MIMM, volume 10)


Herpes genomes are large and complex, with many interactions among herpes encoded proteins, herpes DNA and RNA, and the host cell. These interactions begin as the virus enters the cell, and continue as the decision for latency or lytic replication is made. Correctly regulated gene expression then allows herpes genes to be expressed in a temporally regulated manner and to subvert the host cell metabolism in favor of virus production. Finally, infectious progeny virions are assembled and released. Exploring the function of the many herpes-encoded proteins and the mechanisms to control their expression during these processes thus requires a fine dissection of the herpes genome, so as to allow protein-coding regions to be linked with function and control DNA regions to be identified.


Restriction Site Plasmid Vector Lytic Replication Unique Restriction Site Mutagenic Oligonucleotide 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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Copyright information

© Humana Press Inc., Totowa, NJ 1998

Authors and Affiliations

  • Robert S. Coffin
    • 1
  1. 1.The Windeyer InstituteLondonUK

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