Literature DB >> 8659129

Overexpression of the herpes simplex virus type 1 tegument protein VP22 increases its incorporation into virus particles.

J Leslie1, F J Rixon, J McLauchlan.   

Abstract

The tegument of herpes simplex virus type 1 (HSV-1) virus particles is a complex assemblage of virus proteins whose relative proportions within virions are essentially constant for a particular strain of virus. To examine the processes controlling incorporation into the tegument, we constructed a HSV-1 recombinant that expresses two copies of gene UL49, which encodes the major tegument protein VP22. One copy specifies the unmodified form of VP22 under the control of the native promoter while the second expresses an epitope-tagged version of the protein via the human cytomegalovirus immediate early promoter. In cells infected with the recombinant virus, the overall levels of VP22 synthesized were about fivefold higher than those for wild-type virus, due to the high levels of expression of tagged protein. Analysis of virus particles revealed that the amount of VP22 in the tegument was approximately two- to threefold higher in recombinant virions and L-particles than in particles produced by wild-type virus. These results provide the first evidence that, for certain proteins, the level of polypeptide synthesis can act as a controlling factor for the amount of protein incorporated into tegument.

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Year:  1996        PMID: 8659129     DOI: 10.1006/viro.1996.0286

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  30 in total

1.  Identification of phosphorylation sites within the herpes simplex virus tegument protein VP22.

Authors:  G Elliott; D O'Reilly; P O'Hare
Journal:  J Virol       Date:  1999-07       Impact factor: 5.103

2.  Live-cell analysis of a green fluorescent protein-tagged herpes simplex virus infection.

Authors:  G Elliott; P O'Hare
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

3.  Electrorotation studies of baby hamster kidney fibroblasts infected with herpes simplex virus type 1.

Authors:  S Archer; H Morgan; F J Rixon
Journal:  Biophys J       Date:  1999-05       Impact factor: 4.033

4.  Intercellular delivery of a herpes simplex virus VP22 fusion protein from cells infected with lentiviral vectors.

Authors:  Z Lai; I Han; G Zirzow; R O Brady; J Reiser
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-10       Impact factor: 11.205

5.  Rapid directional translocations in virus replication.

Authors:  Mark Willard
Journal:  J Virol       Date:  2002-05       Impact factor: 5.103

6.  Herpes simplex virus tegument protein VP22 contains overlapping domains for cytoplasmic localization, microtubule interaction, and chromatin binding.

Authors:  Ana Martin; Peter O'Hare; John McLauchlan; Gillian Elliott
Journal:  J Virol       Date:  2002-05       Impact factor: 5.103

7.  Assembly of infectious Herpes simplex virus type 1 virions in the absence of full-length VP22.

Authors:  L E Pomeranz; J A Blaho
Journal:  J Virol       Date:  2000-11       Impact factor: 5.103

8.  The attenuated pseudorabies virus strain Bartha fails to package the tegument proteins Us3 and VP22.

Authors:  Mathew G Lyman; Gretchen L Demmin; Bruce W Banfield
Journal:  J Virol       Date:  2003-01       Impact factor: 5.103

9.  Compartmentalization of VP16 in cells infected with recombinant herpes simplex virus expressing VP16-green fluorescent protein fusion proteins.

Authors:  Sylvie La Boissière; Ander Izeta; Sophie Malcomber; Peter O'Hare
Journal:  J Virol       Date:  2004-08       Impact factor: 5.103

10.  Virion incorporation of the herpes simplex virus type 1 tegument protein VP22 is facilitated by trans-Golgi network localization and is independent of interaction with glycoprotein E.

Authors:  Kevin J O'Regan; Michael J Brignati; Michael A Murphy; Michelle A Bucks; Richard J Courtney
Journal:  Virology       Date:  2010-06-26       Impact factor: 3.616

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