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首页> 外文期刊>Molecular and Cellular Endocrinology >Early induction of the orphan nuclear receptor NOR-1 during cell death of the human breast cancer cell line MCF-7.
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Early induction of the orphan nuclear receptor NOR-1 during cell death of the human breast cancer cell line MCF-7.

机译:在人乳腺癌细胞系MCF-7死亡期间,孤儿核受体NOR-1的早期诱导。

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摘要

The neuron-derived orphan receptor (NOR-1) is a member of the NGFI-B subfamily within the nuclear receptor superfamily. In T-cell apoptosis, where NGFI-B plays an essential role, a functional redundancy between NGFI-B and NOR-1 has been demonstrated. Here, we examined the regulation and expression of the NOR-1 gene during cell death induced by a calcium ionophore A23187 in the human breast cancer cell line MCF-7. A23187 caused a transient increase in NOR-1 mRNA levels within 6 h after treatment. To delineate the sequences required for the transitional response to A23187, a series of promoter deletion mutants were constructed. From the transient transfection experiments, the element responsive to A23187 was identified between -94 and -42 base pairs upstream from the transcription initiation site. This 53-base pairs region contains three copies of the cAMP response element (CRE). Furthermore, phosphorylation of the CRE-binding protein (CREB), which affects the transcription of the CRE dependent-genes, was detected 30 min after A23187 stimulation. Our findings are consistent with NOR-1 involvement in A23187-induced cell death via the CRE-CREB signaling pathway.
机译:神经元孤儿受体(NOR-1)是核受体超家族中NGFI-B亚家族的成员。在NGFI-B发挥重要作用的T细胞凋亡中,已证明NGFI-B和NOR-1之间存在功能冗余。在这里,我们研究了钙离子载体A23187在人乳腺癌细胞系MCF-7中诱导的细胞死亡过程中NOR-1基因的调控和表达。 A23187在治疗后6小时内引起NOR-1 mRNA水平短暂升高。为了描述对A23187的过渡反应所需的序列,构建了一系列启动子缺失突变体。从瞬时转染实验中,在转录起始位点上游的-94和-42个碱基对之间发现了对A23187有反应的元件。这个53个碱基对的区域包含cAMP响应元素(CRE)的三个副本。此外,在A23187刺激后30分钟,检测到CRE结合蛋白(CREB)的磷酸化会影响CRE依赖基因的转录。我们的发现与NOR-1通过CRE-CREB信号通路参与A23187诱导的细胞死亡一致。

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