Section of Molecular Cell and Developmental Biology, Institute for Cellular and Molecular Biology, The University of Texas at Austin, 1 University Station A4800, Austin, TX 78712, USA.
Curr Opin Genet Dev. 2011 Aug;21(4):407-13. doi: 10.1016/j.gde.2011.04.005. Epub 2011 Apr 30.
Localization of mRNAs to subcellular domains can enrich proteins at sites where they function. Coordination with translational control can ensure that the encoded proteins will not appear elsewhere, an important property for factors that control cell fate or body patterning. Here I focus on two aspects of mRNA localization. One is the question of how mRNAs that undergo directed transport by a shared mechanism are bound to the transport machinery, and why localization signals from these mRNAs have very diverse sequences. The second topic concerns the role of particles, in which localized mRNAs often appear. Recent evidence highlights the importance of such assemblies, and the possibility that close association of mRNAs confers community effects and a novel form of regulation.
mRNA 定位于亚细胞域可以使蛋白质在其发挥作用的部位富集。与翻译控制的协调可以确保编码的蛋白质不会出现在其他地方,这对于控制细胞命运或身体模式的因素来说是一个重要的特性。在这里,我关注 mRNA 定位的两个方面。一个是通过共享机制进行定向运输的 mRNAs 如何与运输机制结合的问题,以及为什么这些 mRNAs 的定位信号具有非常不同的序列。第二个主题涉及颗粒的作用,其中经常出现定位的 mRNAs。最近的证据强调了这种组装的重要性,以及密切相关的 mRNAs 赋予群落效应和一种新的调节形式的可能性。