Hsu Felicity Ting-Yu, Smith-Bolton Rachel
Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
bioRxiv. 2025 Mar 16:2025.03.15.643479. doi: 10.1101/2025.03.15.643479.
During the regeneration of injured or lost tissues, the regeneration blastema serves as a hub for robust growth. imaginal discs are a genetically tractable and simple model system for the study of regeneration and organization of this regrowth. Key signals that contribute to regenerative growth in these discs, such as ROS, Wnt/Wg, JNK, p38, JAK/STAT, and the Hippo pathway, have been identified. However, a detailed exploration of the spatial organization of regrowth, the factors that directly drive this growth, and the consequences of activating drivers of regeneration has not been undertaken. Here, we find that regenerative growth in imaginal discs is controlled by the transcription factor Myc and by Tor signaling, which additively drive proliferation and translation in the regeneration blastema. The spatial organization of growth in the blastema is arranged into concentric growth zones defined by Myc expression, elevated Tor activity, and elevated translation. In addition, the increased Myc expression in the innermost zone induced Xrp1-independent cell competition-like death in the adjacent zones, revealing a delicate balance between driving growth and inducing death in the regenerating tissue.
在受损或缺失组织的再生过程中,再生芽基是强劲生长的枢纽。成虫盘是用于研究这种再生和组织再生的遗传易处理且简单的模型系统。已经确定了促成这些盘中再生生长的关键信号,如活性氧(ROS)、Wnt/Wg、JNK、p38、JAK/STAT和Hippo信号通路。然而,尚未对再生的空间组织、直接驱动这种生长的因素以及激活再生驱动因子的后果进行详细探索。在这里,我们发现成虫盘中的再生生长由转录因子Myc和Tor信号传导控制,它们在再生芽基中协同驱动增殖和翻译。芽基中生长的空间组织被排列成由Myc表达、升高的Tor活性和升高的翻译所定义的同心生长区。此外,最内层区域中增加的Myc表达在相邻区域诱导了不依赖Xrp1的细胞竞争样死亡,揭示了在驱动再生组织生长和诱导死亡之间的微妙平衡。