Department of Molecular Biosciences, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX 78712, USA.
Department of Molecular Biosciences, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX 78712, USA
J Cell Sci. 2017 Sep 15;130(18):3060-3071. doi: 10.1242/jcs.202069. Epub 2017 Jul 31.
Localization of mRNAs can involve multiple steps, each with its own -acting localization signals and transport factors. How is the transition between different steps orchestrated? We show that the initial step in localization of mRNA - transport from nurse cells to the oocyte - relies on multiple -acting signals. Some of these are binding sites for the translational control factor Bruno, suggesting that Bruno plays an additional role in mRNA transport. Although transport of mRNA is essential and robust, the localization activity of individual transport signals is weak. Notably, increasing the strength of individual transport signals, or adding a strong transport signal, disrupts the later stages of mRNA localization. We propose that the transport signals are weak by necessity; their weakness facilitates transfer of the mRNA from the oocyte transport machinery to the machinery for posterior localization.
mRNA 的定位可能涉及多个步骤,每个步骤都有其自身作用的定位信号和运输因子。不同步骤之间是如何协调的?我们发现,mRNA 从滋养细胞向卵母细胞运输的初始步骤依赖于多个作用的信号。其中一些是翻译控制因子 Bruno 的结合位点,这表明 Bruno 在 mRNA 运输中发挥了额外的作用。尽管 mRNA 的运输是必需且稳健的,但单个运输信号的定位活性较弱。值得注意的是,增加单个运输信号的强度或添加一个强的运输信号会破坏 mRNA 定位的后期阶段。我们提出,运输信号的弱是必要的;它们的弱点促进了 mRNA 从卵母细胞运输机制向后部定位机制的转移。