Nuk controls pathfinding of commissural axons in the mammalian central nervous system

被引:458
作者
Henkemeyer, M
Orioli, D
Henderson, JT
Saxton, TM
Roder, J
Pawson, T
Klein, R
机构
[1] MT SINAI HOSP,SAMUEL LUNENFELD RES INST,PROGRAMME MOL BIOL & CANC,TORONTO,ON M5G 1X5,CANADA
[2] UNIV TORONTO,DEPT MOLEC & MED GENET,TORONTO,ON M5S 1A8,CANADA
[3] EUROPEAN MOLEC BIOL LAB,D-69117 HEIDELBERG,GERMANY
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0092-8674(00)80075-6
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
Eph family receptor tyrosine kinases have been proposed to control axon guidance and fasciculation. To address the biological functions of the Eph family member Nuk, two mutations in the mouse germline have been generated: a protein null allele (Nuk(1)) and an allele that encodes a Nuk-beta gal fusion receptor lacking the tyrosine kinase and C-terminal domains (Nuk(lacZ)). In Nuk(1) homozygous brains, the majority of axons forming the posterior tract of the anterior commissure migrate aberrantly to the floor of the brain, resulting in a failure of cortical neurons to link the two temporal lobes. These results indicate that Nuk, a receptor that binds transmembrane ligands, plays a critical and unique role in the pathfinding of specific axons in the mammalian central nervous system.
引用
收藏
页码:35 / 46
页数:12
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