Göke Alexandra, Göke Rüdiger, Knolle Anja, Trusheim Heidi, Schmidt Harald, Wilmen Andreas, Carmody Ruaidhri, Göke Burkhard, Chen Youhai H
Clinical Research Unit, University of Marburg, Baldingerstrasse, D-35033, Marburg, Germany
Biochem Biophys Res Commun. 2002 Sep 13;297(1):78-82. doi: 10.1016/s0006-291x(02)02129-0.
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.
为阐明细胞死亡的分子机制,我们从大鼠胰岛素瘤细胞中克隆了一个新基因,命名为死亡上调基因(DUG)。DUG在正常细胞中以极低水平组成性表达,但在血清/葡萄糖饥饿或Fas配体介导的死亡受体连接后,凋亡细胞中其表达显著上调。DUG mRNA存在两种剪接形式:一种长形式编码一个含469个氨基酸的蛋白质,一种短形式产生一个含432个氨基酸的多肽。预测的DUG蛋白序列包含两个假定的核定位信号、多个蛋白激酶的磷酸化位点以及两个保守的MA3结构域。重要的是,DUG与真核生物翻译起始因子(eIF)4G同源,可能通过MA3结构域与eIF4A结合。转染后,DUG抑制凋亡的内源性和外源性途径。因此,DUG是一种调节凋亡的eIF4G新同源物。