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通过bHLH和同源结构域转录因子的直接偶联实现神经发生与运动神经元特化的同步。

Synchronization of neurogenesis and motor neuron specification by direct coupling of bHLH and homeodomain transcription factors.

作者信息

Lee Soo Kyung, Pfaff Samuel L

机构信息

Gene Expression Laboratory, The Salk Institute, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Neuron. 2003 Jun 5;38(5):731-45. doi: 10.1016/s0896-6273(03)00296-4.

Abstract

Inductive signaling leads to the coactivation of regulatory pathways for specifying general neuronal traits in parallel with instructions for neuronal subtype specification. Nevertheless, the mechanisms that ensure that these pathways are synchronized have not been defined. To address this, we examined how bHLH proteins Ngn2 and NeuroM controlling neurogenesis functionally converge with LIM-homeodomain (LIM-HD) factors Isl1 and Lhx3 involved in motor neuron subtype specification. We found that Ngn2 and NeuroM transcriptionally synergize with Isl1 and Lhx3 to specify motor neurons in the embryonic spinal cord and in P19 stem cells. The mechanism underlying this cooperativity is based on interactions that directly couple the activity of the bHLH and LIM-HD proteins, mediated by the adaptor protein NLI. This functional link acts to synchronize neuronal subtype specification with neurogenesis.

摘要

诱导信号传导导致调控通路的共同激活,这些调控通路一方面用于确定一般神经元特征,另一方面用于指导神经元亚型的确定。然而,确保这些通路同步的机制尚未明确。为了解决这个问题,我们研究了控制神经发生的bHLH蛋白Ngn2和NeuroM如何在功能上与参与运动神经元亚型确定的LIM同源域(LIM-HD)因子Isl1和Lhx3相互作用。我们发现,Ngn2和NeuroM在转录水平上与Isl1和Lhx3协同作用,以确定胚胎脊髓和P19干细胞中的运动神经元。这种协同作用的潜在机制基于由衔接蛋白NLI介导的直接连接bHLH和LIM-HD蛋白活性的相互作用。这种功能联系起到使神经元亚型确定与神经发生同步的作用。

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