Bridging Decapentaplegic and Wingless signaling in Drosophila wings through repression of naked cuticle by Brinker

被引:16
|
作者
Yang, Lin [1 ]
Meng, Fei [1 ]
Ma, Da [1 ]
Xie, Wei [1 ]
Fang, Ming [1 ]
机构
[1] Southeast Univ, Inst Life Sci, MOE Key Lab Dev Genes & Human Dis, Nanjing 210096, Jiangsu, Peoples R China
来源
DEVELOPMENT | 2013年 / 140卷 / 02期
关键词
BMP; Brk; Drosophila; Nkd; Wnt; GROWTH-FACTOR-BETA; LONG-RANGE ACTION; MORPHOGEN GRADIENT; TRANSCRIPTIONAL REPRESSOR; DPP; WNT; BINDING; TARGET; EXPRESSION; CATENIN;
D O I
10.1242/dev.082578
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Wnts and bone morphogenetic proteins (BMPs) are signaling elements that are crucial for a variety of events in animal development. In Drosophila, Wingless (Wg, a Wnt ligand) and Decapentaplegic (Dpp, a BMP homolog) are thought to function through distinct signal transduction pathways and independently direct the patterning of the wing. However, recent studies suggest that Mothers against Dpp (Mad), the key transducer of Dpp signaling, might serve as a node for the crosstalk between these two pathways, and both positive and negative roles of Mad in Wg signaling have been suggested. Here, we describe a novel molecular mechanism by which Dpp signaling suppresses Wg outputs. Brinker (Brk), a transcriptional repressor that is downregulated by Dpp, directly represses naked cuticle (nkd), which encodes a feedback inhibitor of Wg signaling, in vitro and in vivo. Through genetic studies, we demonstrate that Brk is required for Wg target gene expression in fly wing imaginal discs and that loss or gain of brk during wing development mimics loss or gain of Wg signaling, respectively. Finally, we show that Dpp positively regulates the expression of nkd and negatively regulates the Wg target gene Distal-less (Dll). These data support a model in which different signaling pathways interact via a negative-feedback mechanism. Such a mechanism might explain how organs coordinate inputs from multiple signaling cues.
引用
收藏
页码:413 / 422
页数:10
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