A new inhibitor of apoptosis from vaccinia virus and eukaryotes

Caroline Gubser, Daniele Bergamaschi, Michael Hollinshead, Xin Lu, Frank J M van Kuppeveld, Geoffrey L Smith

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    A new apoptosis inhibitor is described from vaccinia virus, camelpox virus, and eukaryotic cells. The inhibitor is a hydrophobic, multiple transmembrane protein that is resident in the Golgi and is named GAAP (Golgi anti-apoptotic protein). Stable expression of both viral GAAP (v-GAAP) and human GAAP (h-GAAP), which is expressed in all human tissues tested, inhibited apoptosis induced by intrinsic and extrinsic apoptotic stimuli. Conversely, knockout of h-GAAP by siRNA induced cell death by apoptosis. v-GAAP and h-GAAP display overlapping functions as shown by the ability of v-GAAP to complement for the loss of h-GAAP. Lastly, deletion of the v-GAAP gene from vaccinia virus did not affect virus replication in cell culture, but affected virus virulence in a murine infection model. This study identifies a new regulator of cell death that is highly conserved in evolution from plants to insects, amphibians, mammals, and poxviruses.

    Original languageEnglish
    Pages (from-to)e17
    JournalPLoS Pathogens
    Volume3
    Issue number2
    DOIs
    Publication statusPublished - Feb 2007

    Keywords

    • Amino Acid Sequence
    • Animals
    • Apoptosis
    • Apoptosis Regulatory Proteins
    • Cell Line, Tumor
    • Disease Models, Animal
    • Eukaryotic Cells
    • Female
    • Gene Expression Regulation, Viral
    • Golgi Apparatus
    • HeLa Cells
    • Humans
    • Membrane Proteins
    • Mice
    • Mice, Inbred BALB C
    • Molecular Sequence Data
    • Orthopoxvirus
    • Proteins
    • Vaccinia
    • Vaccinia virus
    • Viral Proteins
    • Virulence
    • Virus Replication

    Fingerprint

    Dive into the research topics of 'A new inhibitor of apoptosis from vaccinia virus and eukaryotes'. Together they form a unique fingerprint.

    Cite this