首页> 美国卫生研究院文献>Molecular and Cellular Biology >Molecular cloning of a human cDNA encoding a novel protein DAD1 whose defect causes apoptotic cell death in hamster BHK21 cells.
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Molecular cloning of a human cDNA encoding a novel protein DAD1 whose defect causes apoptotic cell death in hamster BHK21 cells.

机译:编码新蛋白DAD1的人类cDNA的分子克隆该蛋白的缺陷导致仓鼠BHK21细胞凋亡。

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摘要

The tsBN7 cell line, one of the mutant lines temperature sensitive for growth which have been isolated from the BHK21 cell line, was found to die by apoptosis following a shift to the nonpermissive temperature. The induced apoptosis was inhibited by a protein synthesis inhibitor, cycloheximide, but not by the bcl-2-encoded protein. By DNA-mediated gene transfer, we cloned a cDNA that complements the tsBN7 mutation. It encodes a novel hydrophobic protein, designated DAD1, which is well conserved (100% identical amino acids between humans and hamsters). By comparing the base sequences of the parental BHK21 and tsBN7 DAD1 cDNAs, we found that the DAD1-encoding gene is mutated in tsBN7 cells. The DAD1 protein disappeared in tsBN7 cells following a shift to the nonpermissive temperature, suggesting that loss of the DAD1 protein triggers apoptosis.
机译:tsBN7细胞系是对温度敏感的突变株之一,已从BHK21细胞株中分离出来,发现在转移到非容许温度后,它会因凋亡而死亡。诱导的细胞凋亡受到蛋白质合成抑制剂环己酰亚胺的抑制,但不受bcl-2编码​​的蛋白质的抑制。通过DNA介导的基因转移,我们克隆了一个与tsBN7突变互补的cDNA。它编码称为DAD1的新型疏水蛋白,该蛋白非常保守(人和仓鼠之间100%相同的氨基酸)。通过比较亲代BHK21和tsBN7 DAD1 cDNA的碱基序列,我们发现DAD1编码基因在tsBN7细胞中发生了突变。转变为非许可温度后,tsBN7细胞中的DAD1蛋白消失了,这表明DAD1蛋白的丢失会触发细胞凋亡。

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