Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, UPMC Paris-Sorbonne, 26 Rue d'Ulm, 75005 Paris, France.
Université Côte d'Azur, CNRS UMR7277, Inserm U1091, iBV, Parc Valrose, 06108 Nice, France.
Dev Cell. 2019 Jun 3;49(5):811-818.e4. doi: 10.1016/j.devcel.2019.03.016. Epub 2019 Apr 18.
How organs scale with other body parts is not mechanistically understood. We have addressed this question using the Drosophila imaginal disc model. When the growth of one disc domain is perturbed, other parts of the disc and other discs slow down their growth, maintaining proper inter-disc and intra-disc proportions. We show here that the relaxin-like Dilp8 is required for this inter-organ coordination. Our work also reveals that the stress-response transcription factor Xrp1 plays a key role upstream of dilp8 in linking organ growth status with the systemic growth response. In addition, we show that the small ribosomal subunit protein RpS12 is required to trigger Xrp1-dependent non-autonomous response. Our work demonstrates that RpS12, Xrp1, and Dilp8 form an independent regulatory module that ensures intra- and inter-organ growth coordination during development.
器官与其他身体部位的比例如何变化尚不清楚。我们使用果蝇的胚盘模型来研究这个问题。当一个胚盘区域的生长受到干扰时,胚盘的其他部分和其他胚盘会减缓生长速度,从而维持适当的胚盘间和胚盘内比例。我们在这里表明,类松弛素 Dilp8 对于这种器官间协调是必需的。我们的工作还表明,应激反应转录因子 Xrp1 在将器官生长状态与全身生长反应联系起来方面,在 dilp8 的上游发挥关键作用。此外,我们还表明,核糖体小亚基蛋白 RpS12 是触发 Xrp1 依赖性非自主反应所必需的。我们的工作表明,RpS12、Xrp1 和 Dilp8 形成了一个独立的调控模块,可确保在发育过程中进行器官内和器官间的生长协调。