Serrano (Sano) Functions with the Planar Cell Polarity Genes to Control Tracheal Tube Length

被引:32
作者
Chung, SeYeon [1 ]
Vining, Melissa S. [1 ]
Bradley, Pamela L. [1 ]
Chan, Chih-Chiang [2 ,3 ]
Wharton, Keith A., Jr. [2 ,3 ]
Andrew, Deborah J. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Cell Biol, Baltimore, MD 21218 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
关键词
7-PASS TRANSMEMBRANE CADHERIN; TISSUE POLARITY; DROSOPHILA TRACHEA; POSITIVE SELECTION; SEPTATE JUNCTIONS; SIGNALING PATHWAY; EPITHELIAL-CELLS; HOMEOTIC GENES; SALIVARY-GLAND; SIZE CONTROL;
D O I
10.1371/journal.pgen.1000746
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epithelial tubes are the functional units of many organs, and proper tube geometry is crucial for organ function. Here, we characterize serrano (sano), a novel cytoplasmic protein that is apically enriched in several tube-forming epithelia in Drosophila, including the tracheal system. Loss of sano results in elongated tracheae, whereas Sano overexpression causes shortened tracheae with reduced apical boundaries. Sano overexpression during larval and pupal stages causes planar cell polarity (PCP) defects in several adult tissues. In Sano-overexpressing pupal wing cells, core PCP proteins are mislocalized and prehairs are misoriented; sano loss or overexpression in the eye disrupts ommatidial polarity and rotation. Importantly, Sano binds the PCP regulator Dishevelled (Dsh), and loss or ectopic expression of many known PCP proteins in the trachea gives rise to similar defects observed with loss or gain of sano, revealing a previously unrecognized role for PCP pathway components in tube size control.
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页数:16
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