Formin Proteins of the DAAM Subfamily Play a Role during Axon Growth

被引:77
作者
Matusek, Tamas [1 ]
Gombos, Rita [1 ]
Szecsenyi, Anita [1 ]
Sanchez-Soriano, Natalia [2 ]
Czibula, Agnes [1 ]
Pataki, Csilla [1 ]
Gedai, Anita [1 ]
Prokop, Andreas [2 ]
Rasko, Istvan [1 ]
Mihaly, Jozsef [1 ]
机构
[1] Hungarian Acad Sci, Biol Res Ctr, Inst Genet, H-6726 Szeged, Hungary
[2] Univ Manchester, Fac Life Sci, Wellcome Trust Ctr Cell Matrix Res, Manchester M13 9PT, Lancs, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
axon growth; Formin; dDAAM; filopodia formation; Ena; Profilin; Rac;
D O I
10.1523/JNEUROSCI.2727-08.2008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The regulation of growth cone actin dynamics is a critical aspect of axonal growth control. Among the proteins that are directly involved in the regulation of actin dynamics, actin nucleation factors play a pivotal role by promoting the formation of novel actin filaments. However, the essential nucleation factors in developing neurons have so far not been clearly identified. Here, we show expression data, and use true loss-of-function analysis and targeted expression of activated constructs to demonstrate that the Drosophila formin DAAM plays a critical role in axonal morphogenesis. In agreement with this finding, we show that dDAAM is required for filopodia formation at axonal growth cones. Our genetic interaction, immunoprecipitation and protein localization studies argue that dDAAM acts in concert with Rac GTPases, Profilin and Enabled during axonal growth regulation. We also show that mouse Daam1 rescues the CNS defects observed in dDAAM mutant flies to a high degree, and vice versa, that Drosophila DAAM induces the formation of neurite-like protrusions when expressed in mouse P19 cells, strongly suggesting that the function of DAAM in developing neurons has been conserved during evolution.
引用
收藏
页码:13310 / 13319
页数:10
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