Suppr超能文献

UNC-45A通过控制肌球蛋白II(NMII)的激活来促进神经突的延伸。

UNC-45A is required for neurite extension via controlling NMII activation.

作者信息

Iizuka Yoshie, Mooneyham Ashley, Sieben Andrew, Chen Kevin, Maile Makayla, Hellweg Raffaele, Schütz Florian, Teckle Kebebush, Starr Timothy, Thayanithy Venugopal, Vogel Rachel Isaksson, Lou Emil, Lee Michael K, Bazzaro Martina

机构信息

Masonic Cancer Center and Department of Obstetrics, Gynecology and Women's Heath, University of Minnesota Twin Cities, Minneapolis, MN 55455.

Department of Biology, University of Maryland, Baltimore, MD 21250.

出版信息

Mol Biol Cell. 2017 May 15;28(10):1337-1346. doi: 10.1091/mbc.E16-06-0381. Epub 2017 Mar 29.

Abstract

UNC-45A is a highly conserved member of the UNC-45/CRO1/She4p family of proteins, which act as chaperones for conventional and nonconventional myosins. NMII mediates contractility and actin-based motility, which are fundamental for proper growth cone motility and neurite extension. The presence and role of UNC-45A in neuronal differentiation have been largely unknown. Here we demonstrate that UNC-45A is a novel growth cone--localized, NMII-associated component of the multiprotein complex regulating growth cone dynamics. We show that UNC-45A is dispensable for neuron survival but required for neurite elongation. Mechanistically, loss of UNC-45A results in increased levels of NMII activation. Collectively our results provide novel insights into the molecular mechanisms of neurite growth and define UNC-45A as a novel and master regulator of NMII-mediated cellular processes in neurons.

摘要

UNC-45A是UNC-45/CRO1/She4p蛋白家族中高度保守的成员,该家族蛋白作为传统和非传统肌球蛋白的伴侣蛋白。非肌肉肌球蛋白II(NMII)介导收缩性和基于肌动蛋白的运动性,这对于正常的生长锥运动性和神经突延伸至关重要。UNC-45A在神经元分化中的存在和作用在很大程度上尚不清楚。在此我们证明,UNC-45A是一种新的定位于生长锥的、与NMII相关的多蛋白复合物成分,调节生长锥动力学。我们表明,UNC-45A对神经元存活不是必需的,但对神经突伸长是必需的。从机制上讲,UNC-45A的缺失导致NMII激活水平升高。我们的研究结果共同为神经突生长的分子机制提供了新的见解,并将UNC-45A定义为神经元中NMII介导的细胞过程的一种新的主要调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f9e/5426848/aa62cfc9f92f/1337fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验