DUG is a novel homologue of translation initiation factor 4G that binds eIF4A
Autor: | Anja Knolle, Ruaidhrí J. Carmody, Alexandra Göke, Burkhard Göke, Rüdiger Göke, Youhai H. Chen, Harald Schmidt, Andreas Wilmen, Heidi Trusheim |
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Rok vydání: | 2002 |
Předmět: |
Molecular Sequence Data
Biophysics Gene Expression Apoptosis Biology Biochemistry chemistry.chemical_compound Eukaryotic translation Peptide Initiation Factors Tumor Cells Cultured Protein biosynthesis Animals Initiation factor Amino Acid Sequence Programmed Cell Death Protein 4 Molecular Biology Peptide sequence EIF4G Cell Biology Transfection Molecular biology Rats Up-Regulation chemistry eIF4A Eukaryotic Initiation Factor-4A Apoptosis Regulatory Proteins Carrier Proteins Eukaryotic Initiation Factor-4G |
Zdroj: | Biochemical and Biophysical Research Communications. 297:78-82 |
ISSN: | 0006-291X |
DOI: | 10.1016/s0006-291x(02)02129-0 |
Popis: | To elucidate the molecular mechanisms of cell death, we have cloned a new gene, designated death-upregulated gene (DUG), from rat insulinoma cells. DUG is constitutively expressed at very low levels in normal cells but is dramatically upregulated in apoptotic cells following serum/glucose starvation or death receptor ligation by Fas ligand. The DUG mRNA is present in two splicing forms: a long form that encodes a protein of 469 amino acids and a short form that gives rise to a polypeptide of 432 amino acids. The predicted DUG protein sequence contains two putative nuclear localization signals and multiple phosphorylation sites for protein kinases and two conserved MA3 domains. Importantly, DUG is homologous to eukaryotic translation initiation factor (eIF) 4G and binds to eIF4A presumably through MA3 domains. Upon transfection, DUG inhibits both intrinsic and extrinsic pathways of apoptosis. Thus, DUG is a novel homologue of eIF4G that regulates apoptosis. |
Databáze: | OpenAIRE |
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