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格里姆,果蝇中一个新的细胞死亡基因。

grim, a novel cell death gene in Drosophila.

作者信息

Chen P, Nordstrom W, Gish B, Abrams J M

机构信息

Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235-9039, USA.

出版信息

Genes Dev. 1996 Jul 15;10(14):1773-82. doi: 10.1101/gad.10.14.1773.

Abstract

A genomic interval at 75C1,2 is required for programmed cell death in Drosophila. We identified a new activator of apoptosis, grim, which maps between two previously identified cell death genes in this region reaper (rpr) and head involution defective (hid). Expression of grim RNA coincided with the onset of programmed cell death at all stages of embryonic development, whereas ectopic induction of grim triggered extensive apoptosis in both transgenic animals and in cell culture. Cell killing by grim was blocked by coexpression of p35, a viral product that inactivates ICE-like proteases, and did not require the functions of rpr or hid. The predicted grim protein shares an amino-terminal motif in common with rpr. However, grim was sufficient to elicit apoptosis in at least one context, where rpr was not. The grim gene product might thus function in a parallel circuit of cell death signaling that ultimately activates a common set of downstream apoptotic effectors.

摘要

果蝇中程序性细胞死亡需要位于75C1,2的一个基因组区间。我们鉴定出一种新的凋亡激活因子——严峻基因(grim),它定位于该区域中两个先前已鉴定的细胞死亡基因——收割者基因(rpr)和头部内卷缺陷基因(hid)之间。严峻基因RNA的表达与胚胎发育各个阶段程序性细胞死亡的起始相吻合,而在转基因动物和细胞培养中异位诱导严峻基因会引发广泛的细胞凋亡。严峻基因引发的细胞杀伤作用可被p35(一种使ICE样蛋白酶失活的病毒产物)的共表达所阻断,并且不需要收割者基因或头部内卷缺陷基因的功能。预测的严峻蛋白与收割者蛋白共有一个氨基末端基序。然而,严峻基因在至少一种收割者基因不起作用的情况下足以引发细胞凋亡。因此,严峻基因产物可能在细胞死亡信号传导的平行途径中发挥作用,最终激活一组共同的下游凋亡效应器。

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