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骨形态发生蛋白通过一种涉及转录因子降解的机制抑制神经发生。

BMPs inhibit neurogenesis by a mechanism involving degradation of a transcription factor.

作者信息

Shou J, Rim P C, Calof A L

机构信息

Department of Anatomy & Neurobiology and the Developmental Biology Center, University of California Irvine, College of Medicine, 92697-1275, USA.

出版信息

Nat Neurosci. 1999 Apr;2(4):339-45. doi: 10.1038/7251.

Abstract

Bone morphogenetic proteins (BMPs), negative regulators of neural determination in the early embryo, were found to be potent inhibitors of neurogenesis in olfactory epithelium (OE) cultures. BMPs 2, 4 or 7 decreased the number of proliferating progenitor cells and blocked production of olfactory receptor neurons (ORNs). Experiments suggested that this effect was due to an action of BMPs on an early-stage progenitor in the ORN lineage. Further analysis revealed that progenitors exposed to BMPs rapidly (< 2 h) lost MASH1, a transcription factor known to be required for the production of ORNs. This disappearance was due to proteolysis of existing MASH1 protein, but new gene expression was required to trigger it. The data suggest a novel mechanism of BMP action, whereby the induced degradation of an essential transcription factor results in premature termination of a neuronal lineage.

摘要

骨形态发生蛋白(BMPs)是早期胚胎神经决定的负调节因子,被发现是嗅觉上皮(OE)培养物中神经发生的有效抑制剂。BMPs 2、4或7减少了增殖祖细胞的数量,并阻断了嗅觉受体神经元(ORN)的产生。实验表明,这种作用是由于BMPs对ORN谱系中早期祖细胞的作用。进一步分析显示,暴露于BMPs的祖细胞迅速(<2小时)失去MASH1,MASH1是一种已知的ORN产生所需的转录因子。这种消失是由于现有MASH1蛋白的蛋白水解,但需要新的基因表达来触发它。数据表明了一种BMP作用的新机制,即诱导必需转录因子的降解导致神经元谱系的过早终止。

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