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氨基酸限制诱导CHOP表达既需要ATF4表达,也需要ATF2磷酸化。

Induction of CHOP expression by amino acid limitation requires both ATF4 expression and ATF2 phosphorylation.

作者信息

Averous Julien, Bruhat Alain, Jousse Céline, Carraro Valérie, Thiel Gerald, Fafournoux Pierre

机构信息

Unité de Nutrition et Métabolisme Protéique, Institut National de la Recherche Agronomique de Theix, 63122 Saint Genès Champanelle, France.

出版信息

J Biol Chem. 2004 Feb 13;279(7):5288-97. doi: 10.1074/jbc.M311862200. Epub 2003 Dec 1.

Abstract

The CHOP gene is transcriptionally induced by amino acid starvation. We have previously identified a genomic cis-acting element (amino acid response element (AARE)) involved in the transcriptional activation of the human CHOP gene by leucine starvation and shown that it binds the activating transcription factor 2 (ATF2). The present study was designed to identify other transcription factors capable of binding to the CHOP AARE and to establish their role with regard to induction of the gene by amino acid deprivation. Electrophoretic mobility shift assay and transient transfection experiments show that several transcription factors that belong to the C/EBP or ATF families bind the AARE sequence and activate transcription. Among all these transcription factors, only ATF4 and ATF2 are involved in the amino acid control of CHOP expression. We show that inhibition of ATF2 or ATF4 expression impairs the transcriptional activation of CHOP by amino acid starvation. The transacting capacity of ATF4 depends on its expression level and that of ATF2 on its phosphorylation state. In response to leucine starvation, ATF4 expression and ATF2 phosphorylation are increased. However, induction of ATF4 expression by the endoplasmic reticulum stress pathway does not fully activate the AARE-dependent transcription. Taken together our results demonstrate that at least two pathways, one leading to ATF4 induction and one leading to ATF2 phosphorylation, are necessary to induce CHOP expression by amino acid starvation. This work was extended to the regulation of other amino acid regulated genes and suggests that ATF4 and ATF2 are key components of the amino acid control of gene expression.

摘要

CHOP基因在氨基酸饥饿时会被转录诱导。我们之前已经鉴定出一个基因组顺式作用元件(氨基酸反应元件(AARE)),它参与亮氨酸饥饿对人CHOP基因的转录激活,并表明它能结合激活转录因子2(ATF2)。本研究旨在鉴定其他能够结合CHOP AARE的转录因子,并确定它们在氨基酸剥夺诱导该基因表达方面的作用。电泳迁移率变动分析和瞬时转染实验表明,几个属于C/EBP或ATF家族的转录因子能结合AARE序列并激活转录。在所有这些转录因子中,只有ATF4和ATF2参与CHOP表达的氨基酸调控。我们发现抑制ATF2或ATF4的表达会损害氨基酸饥饿对CHOP的转录激活。ATF4的反式作用能力取决于其表达水平,而ATF2的反式作用能力取决于其磷酸化状态。对亮氨酸饥饿的反应中,ATF4的表达和ATF2的磷酸化会增加。然而,内质网应激途径诱导的ATF4表达并不能完全激活依赖AARE的转录。综合我们的结果表明,至少有两条途径,一条导致ATF4的诱导,一条导致ATF2的磷酸化,是氨基酸饥饿诱导CHOP表达所必需的。这项工作扩展到了对其他氨基酸调控基因的调控,并表明ATF4和ATF2是基因表达氨基酸调控的关键组成部分。

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