Stowers Institute for Medical Research, Kansas City, MO, 64110, USA.
Stowers Institute for Medical Research, Kansas City, MO, 64110, USA; Department of Anatomy and Cell Biology, The University of Kansas School of Medicine, Kansas City, KS, 66160, USA.
Dev Biol. 2022 Aug;488:91-103. doi: 10.1016/j.ydbio.2022.05.008. Epub 2022 May 21.
The Drosophila BMP 2/4 homologue Decapentaplegic (Dpp) acts as a morphogen to regulate diverse developmental processes, including wing morphogenesis. Transcriptional feedback regulation of this pathway ensures tightly controlled signaling outputs to generate the precise pattern of the adult wing. Nevertheless, few direct Dpp target genes have been explored and our understanding of feedback regulation remains incomplete. Here we employ transcriptional profiling following dpp conditional knockout to identify nord, a novel Dpp/BMP feedback regulator. nord mutants generated by CRISPR/Cas9 mutagenesis produce a smaller wing and display low penetrance venation defects. At the molecular level, nord encodes a secreted heparin-binding protein, and we show that its overexpression is sufficient to antagonize Dpp/BMP signaling. Mechanistically, we demonstrate that Nord physically interacts with the Dpp/BMP co-receptor Dally and promotes its degradation. In sum, we propose that Nord fine-tunes Dpp/BMP signaling by regulating Dally availability on the cell surface, with implications for both developmental and disease models.
果蝇 BMP 2/4 同源物 Decapentaplegic (Dpp) 作为一种形态发生素,调节多种发育过程,包括翅膀形态发生。该途径的转录反馈调节确保了信号输出的严格控制,以产生成年翅膀的精确模式。然而,很少有直接的 Dpp 靶基因被探索,我们对反馈调节的理解仍然不完整。在这里,我们采用转录谱分析方法,对 dpp 条件性敲除进行研究,以鉴定 nord,这是一种新的 Dpp/BMP 反馈调节剂。CRISPR/Cas9 诱变产生的 nord 突变体产生较小的翅膀,并显示出低穿透性脉管缺陷。在分子水平上, nord 编码一种分泌性肝素结合蛋白,我们表明其过表达足以拮抗 Dpp/BMP 信号。从机制上讲,我们证明 Nord 通过与 Dpp/BMP 共受体 Dally 的物理相互作用促进其降解。总之,我们提出 Nord 通过调节细胞表面 Dally 的可用性来微调 Dpp/BMP 信号,这对发育和疾病模型都有影响。