Regulation of Axon Guidance by Compartmentalized Nonsense-Mediated mRNA Decay

被引:148
作者
Colak, Dilek [1 ]
Ji, Sheng-Jian [1 ]
Porse, Bo T. [2 ,3 ,4 ]
Jaffrey, Samie R. [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Pharmacol, New York, NY 10065 USA
[2] Univ Copenhagen, Fac Hlth Sci, Finsen Lab, Rigshosp, DK-2200 Copenhagen, Denmark
[3] Univ Copenhagen, BRIC, DK-2200 Copenhagen, Denmark
[4] Univ Copenhagen, Fac Hlth Sci, Danish Stem Cell Ctr DanStem, DK-2200 Copenhagen, Denmark
关键词
LOCAL PROTEIN-SYNTHESIS; COMMISSURAL AXONS; MAMMALIAN-CELLS; MIDLINE SWITCH; SPINAL-CORD; GROWTH CONE; IN-VIVO; TRANSLATION; EXPRESSION; SURVEILLANCE;
D O I
10.1016/j.cell.2013.04.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growth cones enable axons to navigate toward their targets by responding to extracellular signaling molecules. Growth-cone responses are mediated in part by the local translation of axonal messenger RNAs (mRNAs). However, the mechanisms that regulate local translation are poorly understood. Here we show that Robo3.2, a receptor for the Slit family of guidance cues, is synthesized locally within axons of commissural neurons. Robo3.2 translation is induced by floor-plate-derived signals as axons cross the spinal cord midline. Robo3.2 is also a predicted target of the nonsense-mediated mRNA decay (NMD) pathway. We find that NMD regulates Robo3.2 synthesis by inducing the degradation of Robo3.2 transcripts in axons that encounter the floor plate. Commissural neurons deficient in NMD proteins exhibit aberrant axonal trajectories after crossing the midline, consistent with misregulation of Robo3.2 expression. These data show that local translation is regulated by mRNA stability and that NMD acts locally to influence axonal pathfinding.
引用
收藏
页码:1252 / 1265
页数:14
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