Literature DB >> 3283145

Targeting of the hepatitis B virus precore protein to the endoplasmic reticulum membrane: after signal peptide cleavage translocation can be aborted and the product released into the cytoplasm.

P D Garcia1, J H Ou, W J Rutter, P Walter.   

Abstract

The major hepatitis B virus (HBV) core protein is a viral structural protein involved in nucleic acid binding. Its coding sequence contains an extension of 29 codons (the "precore" region) at the amino terminus of the protein which is present in a fraction of the viral transcripts. This region is evolutionarily conserved among mammalian and avian HBVs, suggesting it has functional importance, although at least for duck HBV it has been shown to be nonessential for replication of infectious virions. Using in vitro assays for protein translocation across the endoplasmic reticulum membrane, we found that the precore region of the HBV genome encodes a signal sequence. This signal sequence was recognized by signal recognition particle, which targeted the nascent precore protein to the endoplasmic reticulum membrane with efficiencies comparable to those of other mammalian secretory proteins. A 19-amino acid signal peptide was removed by signal peptidase on the lumenal side of the microsomal membrane, generating a protein similar to the HBV major core protein, but containing 10 additional amino acids from the precore region at its amino terminus. Surprisingly, we found that 70-80% of this signal peptidase-cleaved product was localized on the cytoplasmic side of the microsomal vesicles and was not associated with the membranes. We conclude that translocation was aborted by an unknown mechanism, then the protein disengaged from the translocation machinery and was released back into the cytoplasm. Thus, a cytoplasmically disposed protein was created whose amino terminus resulted from signal peptidase cleavage. The remaining 20-30% appeared to be completely translocated into the lumen of the microsomes. A deletion mutant lacking the carboxy-terminal nucleic acid binding domain of the precore protein was similarly partitioned between the lumen of the microsomes and the cytoplasmic compartment, indicating that this highly charged domain is not responsible for the aborted translocation. We discuss the implications of our findings for the protein translocation process and suggest a possible role in the virus life cycle.

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Year:  1988        PMID: 3283145      PMCID: PMC2114996          DOI: 10.1083/jcb.106.4.1093

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  27 in total

1.  In vitro RNA synthesis with SP6 RNA polymerase.

Authors:  P A Krieg; D A Melton
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

2.  Preparation of microsomal membranes for cotranslational protein translocation.

Authors:  P Walter; G Blobel
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

3.  Cell-free translation of messenger RNA in a wheat germ system.

Authors:  A H Erickson; G Blobel
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

4.  Signal recognition particle: a ribonucleoprotein required for cotranslational translocation of proteins, isolation and properties.

Authors:  P Walter; G Blobel
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

5.  A stop transfer sequence confers predictable transmembrane orientation to a previously secreted protein in cell-free systems.

Authors:  C S Yost; J Hedgpeth; V R Lingappa
Journal:  Cell       Date:  1983-10       Impact factor: 41.582

6.  Isolation of microgram quantities of proteins from polyacrylamide gels for amino acid sequence analysis.

Authors:  M W Hunkapiller; E Lujan; F Ostrander; L E Hood
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

7.  Intracellular protein topogenesis.

Authors:  G Blobel
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

8.  Immunochemical structure of hepatitis B e antigen in the serum.

Authors:  K Takahashi; A Machida; G Funatsu; M Nomura; S Usuda; S Aoyagi; K Tachibana; H Miyamoto; M Imai; T Nakamura; Y Miyakawa; M Mayumi
Journal:  J Immunol       Date:  1983-06       Impact factor: 5.422

9.  Translocation of proteins across the endoplasmic reticulum III. Signal recognition protein (SRP) causes signal sequence-dependent and site-specific arrest of chain elongation that is released by microsomal membranes.

Authors:  P Walter; G Blobel
Journal:  J Cell Biol       Date:  1981-11       Impact factor: 10.539

10.  Translocation of proteins across the endoplasmic reticulum. I. Signal recognition protein (SRP) binds to in-vitro-assembled polysomes synthesizing secretory protein.

Authors:  P Walter; I Ibrahimi; G Blobel
Journal:  J Cell Biol       Date:  1981-11       Impact factor: 10.539

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  72 in total

1.  Molecular analysis of an auxin binding protein gene located on chromosome 4 of Arabidopsis.

Authors:  K Palme; T Hesse; N Campos; C Garbers; M F Yanofsky; J Schell
Journal:  Plant Cell       Date:  1992-02       Impact factor: 11.277

2.  In vitro and in vivo interactions between the hepatitis B virus protein P22 and the cellular protein gC1qR.

Authors:  S Lainé; A Thouard; J Derancourt; M Kress; D Sitterlin; J-M Rossignol
Journal:  J Virol       Date:  2003-12       Impact factor: 5.103

3.  Biosynthesis of the secretory core protein of duck hepatitis B virus: intracellular transport, proteolytic processing, and membrane expression of the precore protein.

Authors:  H J Schlicht
Journal:  J Virol       Date:  1991-07       Impact factor: 5.103

4.  The efficiency of protein compartmentalization into the secretory pathway.

Authors:  Corinna G Levine; Devarati Mitra; Ajay Sharma; Carolyn L Smith; Ramanujan S Hegde
Journal:  Mol Biol Cell       Date:  2004-10-20       Impact factor: 4.138

5.  Protection from cytosolic prion protein toxicity by modulation of protein translocation.

Authors:  Neena S Rane; Jesse L Yonkovich; Ramanujan S Hegde
Journal:  EMBO J       Date:  2004-11-04       Impact factor: 11.598

6.  Characterization of hepatitis B virus capsid particle assembly in Xenopus oocytes.

Authors:  S Zhou; S Q Yang; D N Standring
Journal:  J Virol       Date:  1992-05       Impact factor: 5.103

7.  Evidence for peptide transport across microsomal membranes.

Authors:  B Koppelman; D L Zimmerman; P Walter; F M Brodsky
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-01       Impact factor: 11.205

Review 8.  Avian hepatitis B viruses: molecular and cellular biology, phylogenesis, and host tropism.

Authors:  Anneke Funk; Mouna Mhamdi; Hans Will; Hüseyin Sirma
Journal:  World J Gastroenterol       Date:  2007-01-07       Impact factor: 5.742

9.  Cell-specific metabolism and pathogenesis of transmembrane prion protein.

Authors:  Yaping Gu; Xiu Luo; Subhabrata Basu; Hisashi Fujioka; Neena Singh
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

10.  Biosynthesis and biochemical properties of the hepatitis C virus core protein.

Authors:  E Santolini; G Migliaccio; N La Monica
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

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