NEURAL MIGRATION Structures of netrin-1 bound to two receptors provide insight into its axon guidance mechanism

被引:141
|
作者
Xu, Kai [1 ]
Wu, Zhuhao [2 ]
Renier, Nicolas [2 ]
Antipenko, Alexander [1 ]
Tzvetkova-Robev, Dorothea [1 ]
Xu, Yan [1 ]
Minchenko, Maria [1 ]
Nardi-Dei, Vincenzo [1 ]
Rajashankar, Kanagalaghatta R. [3 ,4 ]
Himanen, Juha [1 ]
Tessier-Lavigne, Marc [2 ]
Nikolov, Dimitar B. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10065 USA
[2] Rockefeller Univ, Lab Brain Dev & Repair, New York, NY 10065 USA
[3] Cornell Univ, Dept Chem & Chem Biol, Argonne, IL 60439 USA
[4] Argonne Natl Lab, Adv Photon Source, Northeastern Collaborat Access Team, Argonne, IL 60439 USA
关键词
HEPARAN-SULFATE; DCC; BINDING; EXPRESSION; FAMILY; MOLECULE; MIDLINE; UNC5; SLIT;
D O I
10.1126/science.1255149
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Netrins are secreted proteins that regulate axon guidance and neuronal migration. Deleted in colorectal cancer (DCC) is a well-established netrin-1 receptor mediating attractive responses. We provide evidence that its close relative neogenin is also a functional netrin-1 receptor that acts with DCC to mediate guidance in vivo. We determined the structures of a functional netrin-1 region, alone and in complexes with neogenin or DCC. Netrin-1 has a rigid elongated structure containing two receptor-binding sites at opposite ends through which it brings together receptor molecules. The ligand/receptor complexes reveal two distinct architectures: a 2:2 heterotetramer and a continuous ligand/receptor assembly. The differences result from different lengths of the linker connecting receptor domains fibronectin type III domain 4 (FN4) and FN5, which differs among DCC and neogenin splice variants, providing a basis for diverse signaling outcomes.
引用
收藏
页码:1275 / 1279
页数:5
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