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LXXLL-Related Motifs in Dax-1 Have Target Specificity for the Orphan Nuclear Receptors Ad4BP/SF-1 and LRH-1

机译:Dax-1中与LXXLL相关的基序对孤儿核受体Ad4BP / SF-1和LRH-1具有靶标特异性

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The orphan receptor Ad4BP/SF-1 (NR5A1) is a constitutive activator, and its activity is repressed by another orphan receptor, Dax-1 (NR0B1). In the present study, we investigated the molecular mechanisms underlying this repression by Dax-1. Yeast two-hybrid and transient-transfection assays confirmed the necessity of three LXXLL-related motifs in Dax-1 for interaction with and repression of Ad4BP/SF-1. In vitro pull-down experiments confirmed that Dax-1 interacts with Ad4BP/SF-1 and also with LRH-1 (NR5A2). The target specificity of the LXXLL-related motifs was indicated by the observations that Ad4BP/SF-1, ERα (NR3A1), LRH-1, ERR2 (NR3B2), and fly FTZ-F1 (NR5A3) interacted through their ligand binding domains with all the LXXLL-related motifs in Dax-1 whereas HNF4 (NR2A1) and RORα (NR1F1) did not. Transcriptional activities of the receptors whose DNA binding domains (DBDs) were replaced by the GAL4 DBD were repressed by Dax-1 to various levels, which correlated with the strength of interaction. Amino acid substitutions revealed that Ad4BP/SF-1 and LRH-1 preferentially interact with L(+1)XXLL-related motifs containing serine, tyrosine, serine, and threonine at positions ?2, +2, +3, and +6, respectively. Taken together, our results indicate that the specificities of LXXLL-related motifs in Dax-1 based on their amino acid sequences play an important role in regulation of orphan receptors.
机译:孤儿受体Ad4BP / SF-1(NR5A1)是组成型激活剂,其活性被另一种孤儿受体Dax-1(NR0B1)抑制。在本研究中,我们研究了Dax-1抑制这种潜在分子机制。酵母双杂交和瞬时转染实验证实,Dax-1中三个与LXXLL相关的基序与Ad4BP / SF-1相互作用和抑制的必要性。体外下拉实验证实,Dax-1与Ad4BP / SF-1以及LRH-1(NR5A2)相互作用。 LXXLL相关基序的靶标特异性由以下观察结果表明:Ad4BP / SF-1,ERα(NR3A1),LRH-1,ERR2(NR3B2)和果蝇FTZ-F1(NR5A3)通过其配体结合结构域与Dax-1中所有LXXLL相关的基序,而HNF4(NR2A1)和RORα(NR1F1)没有。 Dax-1将其DNA结合结构域(DBD)替换为GAL4 DBD的受体的转录活性抑制到各种水平,这与相互作用的强度有关。氨基酸取代显示,Ad4BP / SF-1和LRH-1与L(+1)XXLL相关基序优先相互作用,这些基序在位置α2,+ 2,+ 3和+6处含有丝氨酸,酪氨酸,丝氨酸和苏氨酸,分别。综上所述,我们的结果表明,Dax-1中LXXLL相关基序的特异性基于其氨基酸序列,在孤儿受体的调节中起着重要作用。

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