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c-Myc螺旋-环-螺旋/亮氨酸拉链结构域在小鼠3T3-L1成纤维细胞中诱导细胞凋亡

Induction of apoptosis by the c-Myc helix-loop-helix/leucine zipper domain in mouse 3T3-L1 fibroblasts.

作者信息

Kohlhuber F, Hermeking H, Graessmann A, Eick D

机构信息

Institut für Klinische Molekularbiologie und Tumorgenetik, Forschungszentrum für Umwelt und Gesundheit, GSF, München, Federal Republic of Germany.

出版信息

J Biol Chem. 1995 Dec 1;270(48):28797-805. doi: 10.1074/jbc.270.48.28797.

Abstract

The cellular proto-oncogene c-myc is involved in cell proliferation and transformation but is also implicated in the induction of programmed cell death (apoptosis). The c-Myc protein is a transcriptional activator with a carboxyl-terminal basic region/helix-loop-helix (HLH)/leucine zipper (LZ) domain. It forms heterodimers with the HLH/LZ protein Max and transactivates gene expression after binding DNA E-box elements. We have studied the phenotype of dominant-negative mutants of c-Myc and Max in microinjection experiments. Max mutants with a deleted or mutated basic region inhibited DNA synthesis in serum-stimulated 3T3-L1 mouse fibroblasts. In contrast, mutants of c-Myc expressing only the basic region/HLH/LZ or HLH/LZ domains rapidly induced apoptosis at low and high serum levels. Co-expression of the HLH/LZ domains of c-Myc and Max failed to do so. We suggest that the c-Myc HLH/LZ domain induces apoptosis by specific interaction with cellular factors different to Max.

摘要

细胞原癌基因c-myc参与细胞增殖和转化,但也与程序性细胞死亡(凋亡)的诱导有关。c-Myc蛋白是一种转录激活因子,具有羧基末端碱性区域/螺旋-环-螺旋(HLH)/亮氨酸拉链(LZ)结构域。它与HLH/LZ蛋白Max形成异二聚体,并在结合DNA E-box元件后反式激活基因表达。我们在显微注射实验中研究了c-Myc和Max的显性负性突变体的表型。缺失或突变碱性区域的Max突变体抑制了血清刺激的3T3-L1小鼠成纤维细胞中的DNA合成。相反,仅表达碱性区域/HLH/LZ或HLH/LZ结构域的c-Myc突变体在低血清和高血清水平下均迅速诱导凋亡。c-Myc和Max的HLH/LZ结构域共表达则未能诱导凋亡。我们认为,c-Myc的HLH/LZ结构域通过与不同于Max的细胞因子特异性相互作用来诱导凋亡。

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