The role of C. elegans Ena/VASP homolog UNC-34 in neuronal polarity and motility

被引:24
作者
Fleming, Tinya [1 ]
Chien, Shih-Chieh [1 ]
Vanderzalm, Pamela J. [1 ]
Dell, Megan [1 ]
Gavin, Megan K. [3 ]
Forrester, Wayne C. [4 ]
Garriga, Gian [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
[3] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[4] Indiana Univ, Med Sci Program, Bloomington, IN 47405 USA
基金
美国国家卫生研究院;
关键词
C; elegans; UNC-34; Neuronal polarity; Cell migration; Axon guidance; NEMATODE CAENORHABDITIS-ELEGANS; GROWTH CONE MIGRATIONS; CELL-MIGRATION; AXON GUIDANCE; ASYMMETRIC DISTRIBUTION; FOCAL ADHESION; PROTEIN; MUTATIONS; KINASE; GENES;
D O I
10.1016/j.ydbio.2010.04.025
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ena/VASP proteins mediate the effects of guidance cues on the actin cytoskeleton The single C elegans homolog of the Ena/VASP family of proteins. UNC-34, is required for the migrations of cells and growth cones Here we show that unc-34 mutant alleles also Interact genetically with Wnt mutants to reveal a role for unc-34 in the establishment of neuronal polarity along the C elegans anterior-posterior axis. Our mutant analysis shows that eliminating UNC-34 function results in neuronal migration and polarity phenotypes that are enhanced at higher temperatures, revealing a heat-sensitive process that is normally masked by the presence of UNC-34 Finally, we show that the UNC-34 protein is expressed broadly and accumulates in axons and at the apical junctions of epithelial cells. While most mutants lacked detectable UNC-34. three unc-34 mutants that contained missense mutations in the EVH1 domain produced full-length UNC-34 that failed to localize to apical junctions and axons, supporting the role for the EVH1 domain in localizing Ena/VASP family members (C) 2010 Elsevier Inc All rights reserved
引用
收藏
页码:94 / 106
页数:13
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