Brn-3a转录因子的磷酸化在分化过程中被调节,并调节其功能活性

Mattia Calissano, David Faulkes, David S. Latchman
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引用次数: 7

摘要

Brn-3a是一种在周围神经系统神经元亚群中表达的转录因子。它的作用包括激活参与神经元分化和存活的基因。虽然已经产生了大量关于Brn-3a靶启动子的数据,但对于在分化反应中介导其激活的上游调控信号知之甚少。在这项工作中,我们首次描述了Brn-3a在IMR-32神经母细胞瘤细胞中磷酸化,以响应维甲酸治疗诱导的分化,并且其翻译后修饰可能通过激活MAPK/ERK途径介导。此外,我们还发现,一个假定的磷酸化氨基酸的突变会强烈降低Brn-3a介导IMR-32细胞分化的能力。
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Phosphorylation of the Brn-3a transcription factor is modulated during differentiation and regulates its functional activity

Brn-3a is a transcription factor expressed in a subset of neurons of the peripheral nervous system. Its role encompasses the activation of genes involved in neuronal differentiation and survival. While a lot of data have been produced on Brn-3a target promoters, very little is known about the upstream regulatory signals that mediate its activation in response to differentiation. In this work, we describe for the first time that Brn-3a is phosphorylated in IMR-32 neuroblastoma cells in response to differentiation induced by retinoic acid treatment and that its post-translational modification is potentially mediated by the activation of the MAPK/ERK pathway. Furthermore, we show that the mutation of a putative phosphorylated amino acid strongly reduces the ability of Brn-3a to mediate the differentiation of IMR-32 cells.

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