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一种通过与JNK1相互作用来调节肿瘤坏死因子细胞毒性功能的小尺寸肽Zfra的克隆与特性分析

Cloning and characterization of a small-size peptide Zfra that regulates the cytotoxic function of tumor necrosis factor by interacting with JNK1.

作者信息

Hsu Li-Jin, Schultz Lori, Mattison Jeffrey, Lin Yee-Shin, Chang Nan-Shan

机构信息

Guthrie Research Institute, Laboratory of Molecular Immunology, 1 Guthrie Square, Sayre, PA 18840, USA.

出版信息

Biochem Biophys Res Commun. 2005 Feb 11;327(2):415-23. doi: 10.1016/j.bbrc.2004.12.025.

Abstract

By cDNA library screening, here we isolated an unusual gene transcript encoding a 31-amino-acid zinc finger-like peptide that regulates apoptosis (named Zfra). Northern blotting and RT/PCR showed the transcript is abundant in spleen but absent in several prostate and breast cancer cells. When stably expressed in L929 fibroblasts, Zfra conferred resistance to the cytotoxic effects of TNF and FasL. In contrast, transiently expressed Zfra could enhance or inhibit the cytotoxicity of overexpressed death domain proteins TRADD, FADD, and RIP of the TNF signaling pathway. By GST pull-down assay and co-immunoprecipitation, TNF and UV light were shown to induce Zfra to rapidly self-associate and bind JNK1. While JNK1 is a downstream effector of the TNF signaling, Zfra regulation of the TNF cytotoxic function is likely due to its interaction, in part, with JNK1.

摘要

通过cDNA文库筛选,我们在此分离出一个异常的基因转录本,它编码一种调节细胞凋亡的31个氨基酸的锌指样肽(命名为Zfra)。Northern印迹和RT/PCR显示该转录本在脾脏中丰富,但在几种前列腺癌和乳腺癌细胞中不存在。当在L929成纤维细胞中稳定表达时,Zfra赋予对TNF和FasL细胞毒性作用的抗性。相反,瞬时表达的Zfra可以增强或抑制TNF信号通路中过表达的死亡结构域蛋白TRADD、FADD和RIP的细胞毒性。通过GST下拉试验和免疫共沉淀,显示TNF和紫外线诱导Zfra快速自我缔合并结合JNK1。虽然JNK1是TNF信号的下游效应器,但Zfra对TNF细胞毒性功能的调节可能部分归因于其与JNK1的相互作用。

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