Literature DB >> 28057257

Have NEC Coat, Will Travel: Structural Basis of Membrane Budding During Nuclear Egress in Herpesviruses.

J M Bigalke1, E E Heldwein2.   

Abstract

Herpesviruses are unusual among enveloped viruses because they bud twice yet acquire a single envelope. Furthermore, unlike other DNA viruses that replicate in the nucleus, herpesviruses do not exit it by passing through the nuclear pores or by rupturing the nuclear envelope. Instead, herpesviruses have a complex mechanism of nuclear escape whereby nascent capsids bud at the inner nuclear membrane to form perinuclear virions that subsequently fuse with the outer nuclear membrane, releasing capsids into the cytosol. This makes them some of the very few known viruses that bud into the nuclear envelope. The envelope acquired during nuclear budding does not end up in the mature viral particle but instead allows the capsid to translocate from the nucleus into the cytosol. The viral nuclear egress complex (NEC) is a critical player in the nuclear egress, yet its function and mechanism have remained enigmatic. Recent studies have demonstrated that the NEC buds membranes without the help of other proteins by forming a honeycomb coat, which established the NEC as the first virally encoded budding machine that operates at the nuclear, as opposed to cytoplasmic, membrane. This review discusses our current understanding of the NEC budding mechanism, with the emphasis on studies that illuminated the structure of the NEC coat and its role in capsid budding during herpesvirus nuclear escape.
© 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Budding; Coat; Deenvelopment; Envelopment; Herpesviruses; Hexagonal; Honeycomb; Lattice; NEC; Nuclear egress; Scission; Structure; UL31; UL34

Mesh:

Substances:

Year:  2016        PMID: 28057257      PMCID: PMC5367388          DOI: 10.1016/bs.aivir.2016.07.002

Source DB:  PubMed          Journal:  Adv Virus Res        ISSN: 0065-3527            Impact factor:   9.937


  83 in total

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Authors:  Janna M Bigalke; Ekaterina E Heldwein
Journal:  J Virol       Date:  2015-06-24       Impact factor: 5.103

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Authors:  Lars-Anders Carlson; James H Hurley
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5.  Functional characterization of nuclear trafficking signals in pseudorabies virus pUL31.

Authors:  Lars Paßvogel; Barbara G Klupp; Harald Granzow; Walter Fuchs; Thomas C Mettenleiter
Journal:  J Virol       Date:  2014-12-10       Impact factor: 5.103

6.  Mapping of sequences in Pseudorabies virus pUL34 that are required for formation and function of the nuclear egress complex.

Authors:  Lars Paßvogel; Patricia Trübe; Franziska Schuster; Barbara G Klupp; Thomas C Mettenleiter
Journal:  J Virol       Date:  2013-02-06       Impact factor: 5.103

Review 7.  A structural and functional perspective of alphavirus replication and assembly.

Authors:  Joyce Jose; Jonathan E Snyder; Richard J Kuhn
Journal:  Future Microbiol       Date:  2009-09       Impact factor: 3.165

8.  Identification of conserved amino acids in pUL34 which are critical for function of the pseudorabies virus nuclear egress complex.

Authors:  Lars Paßvogel; Una Janke; Barbara G Klupp; Harald Granzow; Thomas C Mettenleiter
Journal:  J Virol       Date:  2014-03-19       Impact factor: 5.103

9.  Effects of charged cluster mutations on the function of herpes simplex virus type 1 UL34 protein.

Authors:  Susan L Bjerke; John M Cowan; Jelani K Kerr; Ashley E Reynolds; Joel D Baines; Richard J Roller
Journal:  J Virol       Date:  2003-07       Impact factor: 5.103

10.  Deep-etch EM reveals that the early poxvirus envelope is a single membrane bilayer stabilized by a geodetic "honeycomb" surface coat.

Authors:  John Heuser
Journal:  J Cell Biol       Date:  2005-04-25       Impact factor: 10.539

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Authors:  Jenna Barnes; Duncan W Wilson
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Journal:  J Virol       Date:  2020-01-31       Impact factor: 5.103

4.  Comparative Analysis of UL16 Mutants Derived from Multiple Strains of Herpes Simplex Virus 2 (HSV-2) and HSV-1 Reveals Species-Specific Requirements for the UL16 Protein.

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Review 5.  'Come together'-The Regulatory Interaction of Herpesviral Nuclear Egress Proteins Comprises Both Essential and Accessory Functions.

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6.  An ESCRT/VPS4 Envelopment Trap To Examine the Mechanism of Alphaherpesvirus Assembly and Transport in Neurons.

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7.  Importin α1 is required for nuclear import of herpes simplex virus proteins and capsid assembly in fibroblasts and neurons.

Authors:  Katinka Döhner; Ana Ramos-Nascimento; Dagmara Bialy; Fenja Anderson; Ana Hickford-Martinez; Franziska Rother; Thalea Koithan; Kathrin Rudolph; Anna Buch; Ute Prank; Anne Binz; Stefanie Hügel; Robert Jan Lebbink; Rob C Hoeben; Enno Hartmann; Michael Bader; Rudolf Bauerfeind; Beate Sodeik
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Review 8.  Venture from the Interior-Herpesvirus pUL31 Escorts Capsids from Nucleoplasmic Replication Compartments to Sites of Primary Envelopment at the Inner Nuclear Membrane.

Authors:  Susanne M. Bailer
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Journal:  Viruses       Date:  2020-06-24       Impact factor: 5.048

10.  Human Cytomegalovirus Nuclear Capsids Associate with the Core Nuclear Egress Complex and the Viral Protein Kinase pUL97.

Authors:  Jens Milbradt; Eric Sonntag; Sabrina Wagner; Hanife Strojan; Christina Wangen; Tihana Lenac Rovis; Berislav Lisnic; Stipan Jonjic; Heinrich Sticht; William J Britt; Ursula Schlötzer-Schrehardt; Manfred Marschall
Journal:  Viruses       Date:  2018-01-13       Impact factor: 5.048

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