Jiang Hang-Shiang, Han Hsiao-Fen, Chen Cheng-Yi, Hsu Kuan-Lun, Kan Hung-Tsai, Lin Wan-Ying, Wu Mei-Hsuan, Tsai Su-Yi, Wu Jui-Ching, Wu Yi-Chun
Institute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan.
Department of Life Science, National Taiwan University, Taipei, Taiwan.
Cell Death Differ. 2025 Sep 3. doi: 10.1038/s41418-025-01564-x.
Nucleotide metabolism is essential for fundamental cellular functions such as growth, repair and proliferation. Emerging evidence suggests that metabolic pathways also influence programmed cell death (PCD), though the underlying mechanisms remain poorly understood. One model organism that has provided key insights into the regulation of PCD is Caenorhabditis elegans (C. elegans). In this nematode, apoptosis is often initiated through asymmetric cell division (ACD), a process that unequally distributes fate determinants between daughter cells to produce a larger surviving cell and a smaller cell destined for apoptosis. Here, we demonstrate that the simultaneous disruption of PCD and ACD leads to aberrant cell survival and the formation of extra hypodermal cells. Through a genetic screen in the grp-1 ACD mutant background, we identified pyr-1 as a regulator of PCD. pyr-1 encodes the C. elegans carbamoyl-phosphate synthetase/aspartate transcarbamoylase/dihydroorotase (CAD) enzyme which catalyzes the rate-limiting step of de novo pyrimidine biosynthesis, producing uridine 5'-monophosphate (UMP). UMP is a critical metabolite for the synthesis of nucleotides, lipids and carbohydrates. Genetic analysis of UMP metabolic pathways, combined with exogenous nucleoside supplementation, confirms that UMP availability is essential for PYR-1-mediated PCD. Loss of grp-1 induces cellular stress by disrupting fate determinant partitioning during ACD, whereas pyr-1 mutations cause metabolic stress through UMP depletion. While both mutations independently activate autophagy, they function redundantly to upregulate the mitochondrial chaperone hsp-6. Knockdown of autophagy-related genes and hsp-6 reveals that these pathways serve as compensatory mechanisms to protect against cell death in the pyr-1; grp-1 double mutants. Collectively, our findings establish a direct link between metabolism and cell death, demonstrating how UMP availability and proper ACD coordinate apoptotic regulation and developmental outcomes. This study highlights the intricate interplay between metabolic homeostasis and PCD, providing new insights into the metabolic control of cell fate decisions.
核苷酸代谢对于细胞的基本功能如生长、修复和增殖至关重要。新出现的证据表明,代谢途径也会影响程序性细胞死亡(PCD),但其潜在机制仍知之甚少。秀丽隐杆线虫(C. elegans)是一种为PCD调控提供关键见解的模式生物。在这种线虫中,细胞凋亡通常通过不对称细胞分裂(ACD)启动,这一过程在子细胞之间不均等地分配命运决定因子,以产生一个较大的存活细胞和一个较小的注定凋亡的细胞。在这里,我们证明PCD和ACD的同时破坏会导致异常的细胞存活和额外皮下细胞的形成。通过在grp-1 ACD突变体背景下进行遗传筛选,我们确定pyr-1是PCD的一个调节因子。pyr-1编码秀丽隐杆线虫的氨甲酰磷酸合成酶/天冬氨酸转氨甲酰酶/二氢乳清酸酶(CAD),该酶催化从头嘧啶生物合成的限速步骤,产生尿苷5'-单磷酸(UMP)。UMP是核苷酸、脂质和碳水化合物合成的关键代谢物。UMP代谢途径的遗传分析,结合外源核苷补充,证实UMP的可用性对于PYR-1介导的PCD至关重要。grp-1的缺失通过破坏ACD过程中的命运决定因子分配诱导细胞应激,而pyr-1突变则通过UMP耗竭导致代谢应激。虽然这两种突变都独立激活自噬,但它们在功能上冗余地上调线粒体伴侣hsp-6。自噬相关基因和hsp-6的敲低表明,这些途径作为补偿机制,保护pyr-1;grp-1双突变体中的细胞免于死亡。总体而言,我们的发现建立了代谢与细胞死亡之间的直接联系,证明了UMP可用性和适当的ACD如何协调细胞凋亡调控和发育结果。这项研究突出了代谢稳态与PCD之间的复杂相互作用,为细胞命运决定的代谢控制提供了新的见解。