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UNC-6/网蛋白受体UNC-40/结直肠癌缺失基因(DCC)和UNC-5通过UNC-73/三重奏蛋白、类Rac鸟苷三磷酸酶和UNC-33/CRMP抑制生长锥丝状伪足的突出。

The UNC-6/Netrin receptors UNC-40/DCC and UNC-5 inhibit growth cone filopodial protrusion via UNC-73/Trio, Rac-like GTPases and UNC-33/CRMP.

作者信息

Norris Adam D, Sundararajan Lakshmi, Morgan Dyan E, Roberts Zachary J, Lundquist Erik A

机构信息

Programs in Genetics and Molecular, Cellular, and Developmental Biology, Department of Molecular Biosciences, The University of Kansas, 1200 Sunnyside Avenue, Lawrence, KS 66045, USA.

Programs in Genetics and Molecular, Cellular, and Developmental Biology, Department of Molecular Biosciences, The University of Kansas, 1200 Sunnyside Avenue, Lawrence, KS 66045, USA

出版信息

Development. 2014 Nov;141(22):4395-405. doi: 10.1242/dev.110437.

Abstract

UNC-6/Netrin is a conserved axon guidance cue that can mediate both attraction and repulsion. We previously discovered that attractive UNC-40/DCC receptor signaling stimulates growth cone filopodial protrusion and that repulsive UNC-40-UNC-5 heterodimers inhibit filopodial protrusion in C. elegans. Here, we identify cytoplasmic signaling molecules required for UNC-6-mediated inhibition of filopodial protrusion involved in axon repulsion. We show that the Rac-like GTPases CED-10 and MIG-2, the Rac GTP exchange factor UNC-73/Trio, UNC-44/Ankyrin and UNC-33/CRMP act in inhibitory UNC-6 signaling. These molecules were required for the normal limitation of filopodial protrusion in developing growth cones and for inhibition of growth cone filopodial protrusion caused by activated MYR::UNC-40 and MYR::UNC-5 receptor signaling. Epistasis studies using activated CED-10 and MIG-2 indicated that UNC-44 and UNC-33 act downstream of the Rac-like GTPases in filopodial inhibition. UNC-73, UNC-33 and UNC-44 did not affect the accumulation of full-length UNC-5::GFP and UNC-40::GFP in growth cones, consistent with a model in which UNC-73, UNC-33 and UNC-44 influence cytoskeletal function during growth cone filopodial inhibition.

摘要

UNC-6/Netrin是一种保守的轴突导向信号分子,既能介导吸引作用,也能介导排斥作用。我们之前发现,具有吸引作用的UNC-40/DCC受体信号传导可刺激生长锥丝状伪足的伸出,而具有排斥作用的UNC-40-UNC-5异二聚体则会抑制秀丽隐杆线虫中丝状伪足的伸出。在此,我们鉴定出了UNC-6介导的、参与轴突排斥的丝状伪足伸出抑制过程所需的细胞质信号分子。我们发现,类Rac GTP酶CED-10和MIG-2、Rac GTP交换因子UNC-73/Trio、UNC-44/锚蛋白和UNC-33/CRMP在具有抑制作用的UNC-6信号传导中发挥作用。这些分子对于发育中的生长锥丝状伪足伸出的正常限制以及由活化的MYR::UNC-40和MYR::UNC-5受体信号传导引起的生长锥丝状伪足伸出的抑制是必需的。使用活化的CED-10和MIG-2进行的上位性研究表明,在丝状伪足抑制过程中,UNC-44和UNC-33在类Rac GTP酶的下游发挥作用。UNC-73、UNC-33和UNC-44并不影响全长UNC-5::GFP和UNC-40::GFP在生长锥中的积累,这与UNC-73、UNC-33和UNC-44在生长锥丝状伪足抑制过程中影响细胞骨架功能的模型一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a52/4302909/64ef583cad32/develop-141-110437-g1.jpg

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