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孤儿核受体NR3B家族与NR4A家族之间的相互作用。

Cross-talk between the NR3B and NR4A families of orphan nuclear receptors.

作者信息

Lammi Johanna, Rajalin Ann-Marie, Huppunen Johanna, Aarnisalo Piia

机构信息

Institute of Biomedicine, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland.

出版信息

Biochem Biophys Res Commun. 2007 Jul 27;359(2):391-7. doi: 10.1016/j.bbrc.2007.05.122. Epub 2007 May 25.

Abstract

Estrogen-related receptors (NR3B family) and Nurr1, NGFI-B, and Nor1 (NR4A family) are orphan nuclear receptors lacking identified natural ligands. The mechanisms regulating their transcriptional activities have remained elusive. We have previously observed that the members of NR3B and NR4A families are coexpressed in certain cell types such as osteoblasts and that the ability of Nurr1 to transactivate the osteopontin promoter is repressed by ERRs. We have now studied the cross-talk between NR3B and NR4A receptors. We show that NR3B and NR4A receptors mutually repress each others' transcriptional activity. The repression involves intact DNA-binding domains and dimerization interfaces but does not result from competition for DNA binding or from heterodimerization. The activation functions of NR3B and NR4A receptors are dispensable for the cross-talk. In conclusion, we report that cross-talk between NR3B and NR4A receptors is a mechanism modulating the transcriptional activities of these orphan nuclear receptors.

摘要

雌激素相关受体(NR3B家族)以及Nurr1、NGFI-B和Nor1(NR4A家族)是缺乏已确定天然配体的孤儿核受体。调节它们转录活性的机制一直难以捉摸。我们之前观察到,NR3B和NR4A家族的成员在某些细胞类型(如成骨细胞)中共同表达,并且ERRs会抑制Nurr1反式激活骨桥蛋白启动子的能力。我们现在研究了NR3B和NR4A受体之间的相互作用。我们发现NR3B和NR4A受体相互抑制彼此的转录活性。这种抑制涉及完整的DNA结合结构域和二聚化界面,但并非由对DNA结合的竞争或异源二聚化导致。NR3B和NR4A受体的激活功能对于这种相互作用并非必需。总之,我们报告NR3B和NR4A受体之间的相互作用是一种调节这些孤儿核受体转录活性的机制。

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