Rodrigues Elsa C, Grawenhoff Julia, Baumann Sebastian J, Lorenzon Nicola, Maurer Sebastian P
Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Front Integr Neurosci. 2021 Jun 15;15:692948. doi: 10.3389/fnint.2021.692948. eCollection 2021.
Hundreds of messenger RNAs (mRNAs) are transported into neurites to provide templates for the assembly of local protein networks. These networks enable a neuron to configure different cellular domains for specialized functions. According to current evidence, mRNAs are mostly transported in rather small packages of one to three copies, rarely containing different transcripts. This opens up fascinating logistic problems: how are hundreds of different mRNA cargoes sorted into distinct packages and how are they coupled to and released from motor proteins to produce the observed mRNA distributions? Are all mRNAs transported by the same transport machinery, or are there different adaptors or motors for different transcripts or classes of mRNAs? A variety of often indirect evidence exists for the involvement of proteins in mRNA localization, but relatively little is known about the essential activities required for the actual transport process. Here, we summarize the different types of available evidence for interactions that connect mammalian mRNAs to motor proteins to highlight at which point further research is needed to uncover critical missing links. We further argue that a combination of discovery approaches reporting direct interactions, reconstitution, and fast perturbations in cells is an ideal future strategy to unravel essential interactions and specific functions of proteins in mRNA transport processes.
数百种信使核糖核酸(mRNA)被转运到神经突中,为局部蛋白质网络的组装提供模板。这些网络使神经元能够为特定功能配置不同的细胞结构域。根据目前的证据,mRNA大多以一至三个拷贝的相当小的包裹形式运输,很少包含不同的转录本。这引发了一些引人入胜的物流问题:数百种不同的mRNA货物是如何被分类到不同的包裹中的,以及它们如何与运动蛋白结合并从运动蛋白上释放,以产生观察到的mRNA分布?所有的mRNA都是由相同的运输机制运输的,还是针对不同的转录本或mRNA类别存在不同的衔接蛋白或马达蛋白?有各种往往是间接的证据表明蛋白质参与了mRNA定位,但对于实际运输过程所需的基本活动却知之甚少。在这里,我们总结了将哺乳动物mRNA与运动蛋白联系起来的相互作用的不同类型的现有证据,以突出在哪些方面需要进一步研究以揭示关键的缺失环节。我们进一步认为,报告直接相互作用、重组和细胞快速扰动的发现方法相结合,是未来揭示蛋白质在mRNA运输过程中的基本相互作用和特定功能的理想策略。