Regulation of long-range planar cell polarity by Fat-Dachsous signaling

被引:22
作者
Sharma, Praveer [1 ,2 ]
McNeill, Helen [1 ,2 ]
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
来源
DEVELOPMENT | 2013年 / 140卷 / 18期
基金
加拿大健康研究院;
关键词
Atrophin; Dachsous; Drosophila; Fat; PCP; Polarity; DROSOPHILA EYE; TUMOR-SUPPRESSOR; CADHERIN SUPERFAMILY; PROTOCADHERINS FAT; PROMOTES APOPTOSIS; WING EPITHELIUM; GROWTH; PATHWAY; HIPPO; GENE;
D O I
10.1242/dev.094730
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fat (Ft) and Dachsous (Ds) are large cadherins that bind each other and have conserved roles in regulating planar cell polarity (PCP). We quantitatively analyzed Ft-Ds pathway mutant clones for their effects on ommatidial polarity in the Drosophila eye. Our findings suggest that the Ft-Ds pathway regulates PCP propagation independently of asymmetric cellular accumulation of Ft or Ds. We find that the Ft effector Atrophin has a position-specific role in regulating polarity in the eye, and that asymmetric accumulation of the atypical myosin Dachs is not essential for production and propagation of a long-range PCP signal. Our observations suggest that Ft and Ds interact to modulate a secondary signal that regulates long-range polarity, that signaling by the Ds intracellular domain is dependent on Ft, and that ommatidial fate specification is genetically separable from long-range signaling.
引用
收藏
页码:3869 / 3881
页数:13
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