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Differential Regulation of Transcription by the NURR1/NUR77 Subfamily of Nuclear Transcription Factors

机译:NURR1 / NUR77核转录因子亚家族对转录的差异调节

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摘要

NURR1 is an orphan member of the nuclear receptor superfamily of transcription factors that shares close sequence homology to the orphan nuclear receptor and immediate early gene product NUR77(NGF1β). The physiological role of NURR1 has not been established in mammalian cells. However, the observation that NURR1 and NUR77 interact with at least one common enhancer element (AAAAGGTCA), together with their partly overlapping but differential expression patterns in mammalian tissues, suggests that these proteins may have both shared and independent transcription regulatory functions. To identify potential target genes that may be regulated by NURR1, we analyzed its DNA binding properties to potential cis-acting enhancer elements. Using point mutagenesis of the AAAAGGTCA motif, we have identified three additional sequences that bind specifically to both NURR1 and NUR77, one of which serves as a functional enhancer element. Comparative analysis of the transcription regulatory properties of NURR1 and NUR77 indicates that the proteins can display opposing transregulatory activities that are influenced by the specific os-acting sequences to which they bind. Our results indicate that the transcriptional responses of specific target genes to the NURR1/NUR77 subfamily may be differentially regulated by the relative cellular levels of NURR1 and NUR77 and influenced by the specific enhancer sequences that mediate their activity. Finally, we have identified several potential target genes of neuronal and neuroendocrine origin whose promoters contain this element.
机译:NURR1是转录因子核受体超家族的一个孤儿,与孤儿核受体和直接早期基因产物NUR77(NGF1β)有着紧密的序列同源性。 NURR1的生理作用尚未在哺乳动物细胞中确立。但是,观察到NURR1和NUR77与至少一个共同的增强子(AAAAGGTCA)相互作用,以及它们在哺乳动物组织中部分重叠但差异表达的模式,表明这些蛋白质可能具有共享和独立的转录调控功能。为了确定可能受NURR1调控的潜在靶基因,我们分析了其与潜在的顺式作用增强子元件的DNA结合特性。使用AAAAGGTCA基序的点诱变,我们鉴定了三个与NURR1和NUR77特异性结合的其他序列,其中一个充当功能增强子。 NURR1和NUR77的转录调节特性的比较分析表明,这些蛋白可以显示相反的反式调节活性,这些活性受它们结合的特定os-作用序列的影响。我们的结果表明,特定靶基因对NURR1 / NUR77亚家族的转录反应可能受到NURR1和NUR77相对细胞水平的差异调节,并受到介导其活性的特定增强子序列的影响。最后,我们确定了神经元和神经内分泌来源的几个潜在靶基因,其启动子包含该元件。

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