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 language | English |
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Pages (from-to) | e17 |
Journal | PLoS Pathogens |
Volume | 3 |
Issue number | 2 |
DOIs | |
Publication status | Published - 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