Orbán-Németh Zsuzsanna, Simader Hannes, Badurek Sylvia, Tranciková Alzbeta, Propst Friedrich
Institute of Biochemistry and Molecular Cell Biology, Vienna Biocenter, University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
J Biol Chem. 2005 Jan 21;280(3):2257-65. doi: 10.1074/jbc.M408984200. Epub 2004 Nov 4.
The related high molecular mass microtubule-associated proteins (MAPs) MAP1A and MAP1B are predominantly expressed in the nervous system and are involved in axon guidance and synaptic function. MAP1B is implicated in fragile X mental retardation, giant axonal neuropathy, and ataxia type 1. We report the functional characterization of a novel member of the microtubule-associated protein 1 family, which we termed MAP1S (corresponding to sequence data bank entries for VCY2IP1 and C19ORF5). MAP1S contains the three hallmark domains of the microtubule-associated protein 1 family but hardly any additional sequences. It decorates neuronal microtubules and copurifies with tubulin from brain. MAP1S is synthesized as a precursor protein that is partially cleaved into heavy and light chains in a tissue-specific manner. Heavy and light chains interact to form the MAP1S complex. The light chain binds, bundles, and stabilizes microtubules and binds to actin. The heavy chain appears to regulate light chain activity. In contrast to MAP1A and MAP1B, MAP1S is expressed in a wide range of tissues in addition to neurons and represents the non-neuronal counterpart of this cytolinker family.
相关的高分子量微管相关蛋白(MAPs)MAP1A和MAP1B主要在神经系统中表达,并参与轴突导向和突触功能。MAP1B与脆性X智力低下、巨大轴索性神经病和1型共济失调有关。我们报告了微管相关蛋白1家族一个新成员的功能特征,我们将其命名为MAP1S(对应于序列数据库中VCY2IP1和C19ORF5的条目)。MAP1S包含微管相关蛋白1家族的三个标志性结构域,但几乎没有其他序列。它修饰神经元微管,并与脑中的微管蛋白共纯化。MAP1S以前体蛋白形式合成,该前体蛋白以组织特异性方式部分切割成重链和轻链。重链和轻链相互作用形成MAP1S复合物。轻链结合、捆绑并稳定微管,并与肌动蛋白结合。重链似乎调节轻链活性。与MAP1A和MAP1B不同,MAP1S除了在神经元中表达外,还在多种组织中表达,代表了这个细胞连接蛋白家族的非神经元对应物。