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首页> 外文期刊>Development >The conserved kinase UNC-51 acts with VAB-8 and UNC-14 to regulate axon outgrowth in C. elegans.
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The conserved kinase UNC-51 acts with VAB-8 and UNC-14 to regulate axon outgrowth in C. elegans.

机译:保守的激酶UNC-51与VAB-8和UNC-14一起作用以调节秀丽隐杆线虫的轴突生长。

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摘要

Directional cues guide growth cones. While molecules like UNC-6/netrin direct migrations along the dorsoventral axis of many organisms, it is unclear how anteroposterior guidance is achieved. We describe a physical interaction between VAB-8, a protein both necessary and sufficient for posteriorly directed migrations in C. elegans, and UNC-51, a conserved serine/threonine kinase that functions generally in axon outgrowth. We show that both proteins function in the CAN neurons to direct their axons posteriorly. Expression in the CANs of peptides predicted to interfere with interactions between UNC-51 and both VAB-8 and UNC-14, a second protein that interacts physically with UNC-51, disrupts CAN axon outgrowth. We provide genetic evidence that VAB-8 functions in an UNC-51 pathway for posteriorly directed CAN axon guidance and show that VAB-8 and UNC-14 can be targets of UNC-51 kinase activity. Taken together, our results suggest that VAB-8 and UNC-14 are substrates that mediate the function of UNC-51 in axon outgrowth.
机译:方向提示引导生长锥。虽然像UNC-6 / netrin这样的分子直接沿许多生物的背腹轴迁移,但不清楚如何实现前后引导。我们描述了VAB-8和UNC-51之间的物理相互作用,VAB-8是在秀丽隐杆线虫中进行后向迁移所必需和充分的蛋白质,UNC-51是一种保守的丝氨酸/苏氨酸激酶,通常在轴突生长中起作用。我们显示这两种蛋白质在CAN神经元中的功能,以指导其轴突向后。预测会干扰UNC-51与VAB-8和UNC-14之间相互作用的肽在CAN中的表达是与UNC-51物理相互作用的第二种蛋白质,可干扰CAN轴突的生长。我们提供了遗传证据,表明VAB-8在UNC-51途径中对后向CAN轴突的指导起作用,并表明VAB-8和UNC-14可以成为UNC-51激酶活性的目标。两者合计,我们的结果表明,VAB-8和UNC-14是在轴突生长中介导UNC-51功能的底物。

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