Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Department of Molecular Neurobiology, Madrid, Spain.
EMBO J. 2013 May 2;32(9):1293-306. doi: 10.1038/emboj.2013.76. Epub 2013 Apr 9.
MAP1B, a structural microtubule (MT)-associated protein highly expressed in developing neurons, plays a key role in neurite and axon extension. However, not all molecular mechanisms by which MAP1B controls MT dynamics during these processes have been revealed. Here, we show that MAP1B interacts directly with EB1 and EB3 (EBs), two core 'microtubule plus-end tracking proteins' (+TIPs), and sequesters them in the cytosol of developing neuronal cells. MAP1B overexpression reduces EBs binding to plus-ends, whereas MAP1B downregulation increases binding of EBs to MTs. These alterations in EBs behaviour lead to changes in MT dynamics, in particular overstabilization and looping, in growth cones of MAP1B-deficient neurons. This contributes to growth cone remodelling and a delay in axon outgrowth. Together, our findings define a new and crucial role of MAP1B as a direct regulator of EBs function and MT dynamics during neurite and axon extension. Our data provide a new layer of MT regulation: a classical MAP, which binds to the MT lattice and not to the end, controls effective concentration of core +TIPs thereby regulating MTs at their plus-ends.
MAP1B 是一种在发育神经元中高度表达的结构微管 (MT) 相关蛋白,在轴突和树突延伸中发挥关键作用。然而,并非 MAP1B 在这些过程中控制 MT 动态的所有分子机制都已被揭示。在这里,我们表明 MAP1B 直接与 EB1 和 EB3(EBs)相互作用,EBs 是两种核心的“微管正端追踪蛋白”(+TIPs),并将它们隔离在发育神经元细胞的细胞质中。MAP1B 的过表达减少了 EBs 与正端的结合,而 MAP1B 的下调增加了 EBs 与 MT 的结合。EBs 行为的这些改变导致生长锥中 MT 动态的变化,特别是过度稳定和环化,在 MAP1B 缺失神经元的生长锥中。这有助于生长锥重塑和轴突生长的延迟。总之,我们的发现定义了 MAP1B 作为直接调节 EB 功能和微管动力学的新的和关键作用,在轴突和树突延伸过程中。我们的数据提供了微管调节的新层面:一种经典的 MAP,它与 MT 晶格结合而不是与末端结合,控制核心 +TIPs 的有效浓度,从而调节 MT 在其正端。