Drosophila Cappuccino alleles provide insight into formin mechanism and role in oogenesis

被引:9
|
作者
Yoo, Haneul [1 ]
Roth-Johnson, Elizabeth A. [2 ]
Bor, Batbileg [2 ]
Quinlan, Margot E. [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Mol Biol Interdept PhD Program, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
BARBED-END ASSOCIATION; 2 ACTIN NUCLEATORS; HOMOLOGY-2; DOMAIN; SPIRE; MICROTUBULE; POLARITY; PROTEIN; PHOSPHORYLATION; POLYMERASE; OOCYTES;
D O I
10.1091/mbc.E14-11-1558
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During Drosophila development, the formin actin nucleator Cappuccino (Capu) helps build a cytoplasmic actin mesh throughout the oocyte. Loss of Capu leads to female sterility, presumably because polarity determinants fail to localize properly in the absence of the mesh. To gain deeper insight into how Capu builds this actin mesh, we systematically characterized seven capu alleles, which have missense mutations in Capu's formin homology 2 (FH2) domain. We report that all seven alleles have deleterious effects on fly fertility and the actin mesh in vivo but have strikingly different effects on Capu's biochemical activity in vitro. Using a combination of bulk and single-filament actin-assembly assays, we find that the alleles differentially affect Capu's ability to nucleate and processively elongate actin filaments. We also identify a unique "loop" in the lasso region of Capu's FH2 domain. Removing this loop enhances Capu's nucleation, elongation, and F-actin-bundling activities in vitro. Together our results on the loop and the seven missense mutations provides mechanistic insight into formin function in general and Capu's role in the Drosophila oocyte in particular.
引用
收藏
页码:1875 / 1886
页数:12
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