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佛波酯介导的一种干扰素诱导基因的下调

Phorbol ester-mediated down-regulation of an interferon-inducible gene.

作者信息

Akai H, Larner A C

机构信息

Laboratory of Pathology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1989 Feb 25;264(6):3252-5.

PMID:2464596
Abstract

Interferons (IFNs) induce the expression of a variety of cellular RNAs and inhibit phorbol ester induction of other genes. Experiments reported here indicate that phorbol esters can also specifically inhibit the expression of an IFN-induced RNA (IFN-IND-1). Phorbol esters exert their effects by inhibiting IFN-induced transcription of the gene that encodes IFN-IND-1 (ISG-54K); inhibitors of protein synthesis reverse the effects of these compounds. The actions of phorbol esters are only seen in those types of cultured cells where cycloheximide in the presence of IFN prevents long term IFN treatment of cells from inducing a "desensitized state." In desensitized cells, IFN is not able to reinduce the transcription of the RNA. Our results indicate that a protein kinase C-dependent pathway requiring protein synthesis may be one mechanism by which IFN is able to down regulate the transcription of genes whose expression it initially induces.

摘要

干扰素(IFN)可诱导多种细胞RNA的表达,并抑制佛波酯对其他基因的诱导作用。本文报道的实验表明,佛波酯也能特异性抑制一种干扰素诱导的RNA(IFN-IND-1)的表达。佛波酯通过抑制编码IFN-IND-1(ISG-54K)的基因的干扰素诱导转录发挥作用;蛋白质合成抑制剂可逆转这些化合物的作用。佛波酯的作用仅在那些在干扰素存在下环己酰亚胺可防止细胞长期接受干扰素处理而诱导“脱敏状态”的培养细胞类型中可见。在脱敏细胞中,干扰素无法再次诱导该RNA的转录。我们的结果表明,一种依赖蛋白激酶C且需要蛋白质合成的途径可能是干扰素下调其最初诱导表达的基因转录的一种机制。

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