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Jun/AP-1的负调控:糖原合酶激酶3和果蝇激酶shaggy的保守功能

Negative regulation of Jun/AP-1: conserved function of glycogen synthase kinase 3 and the Drosophila kinase shaggy.

作者信息

de Groot R P, Auwerx J, Bourouis M, Sassone-Corsi P

机构信息

Laboratoire de Génétique Moléculaire des Eucaryotes de CNRS, Unité 184 de l'INSERM, Faculté de Médecine, Strasbourg, France.

出版信息

Oncogene. 1993 Apr;8(4):841-7.

PMID:8384355
Abstract

Transcription factor AP-1 is constituted by the products of the various fos and jun genes. AP-1 activity is modulated by second messengers and appears to involve post-translational modifications of Fos and Jun. It has been shown that phosphorylation mediated by glycogen synthase kinase 3 (GSK-3) is involved in negative regulation of c-Jun DNA-binding function in vitro. Here we show that two forms of GSK-3 function to decrease the DNA-binding activity as well as the transcriptional activation elicited by c-Jun in vivo. Similarly, the other members of the jun family, JunB, JunD and v-Jun, are negatively regulated by GSK-3 in vivo, although to a slightly lesser extent than c-Jun. We have also tested the proteins encoded by the Drosophila shaggy gene (sgg) in our assays. The sgg proteins share homology with the mammalian GSK-3 and appear to be important for the normal segregation of bristle precursor cells in the imaginal epithelium in Drosophila. Here we show that the products of the sgg gene can also function as negative regulators of Jun/AP-1.

摘要

转录因子AP-1由多种fos和jun基因的产物组成。AP-1的活性受第二信使调节,似乎涉及Fos和Jun的翻译后修饰。研究表明,糖原合酶激酶3(GSK-3)介导的磷酸化在体外参与c-Jun DNA结合功能的负调控。在此我们表明,两种形式的GSK-3在体内发挥作用,降低c-Jun引发的DNA结合活性以及转录激活。同样,jun家族的其他成员JunB、JunD和v-Jun在体内也受GSK-3的负调控,尽管程度略低于c-Jun。我们还在实验中测试了果蝇蓬乱基因(sgg)编码的蛋白质。sgg蛋白与哺乳动物的GSK-3具有同源性,似乎对果蝇成虫上皮中刚毛前体细胞的正常分离很重要。在此我们表明,sgg基因的产物也可作为Jun/AP-1的负调控因子。

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