School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
State Key Laboratory of Cell Biology, Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai 200031, China.
Int J Mol Sci. 2024 Jan 25;25(3):1453. doi: 10.3390/ijms25031453.
CTP synthase (CTPS), the rate-limiting enzyme in the de novo synthesis of CTP, assembles into a filamentous structure termed the cytoophidium. The Hippo pathway regulates cell proliferation and apoptosis. The relationship of the nucleotide metabolism with the Hippo pathway is little known. Here, we study the impact of the Hippo pathway on the cytoophidium in posterior follicle cells (PFCs). We find that the inactivation of the Hippo pathway correlates with reduced cytoophidium length and number within PFCs. During the overexpression of CTPS, the presence of Hippo mutations also reduces the length of cytoophidia in PFCs. In addition, we observe that knocking down CTPS mitigates (Hippo)-associated over-proliferation. In summary, our results suggest that there is a connection between the Hippo pathway and the nucleotide biosynthesis enzyme CTPS in PFCs.
CTP 合酶(CTPS)是从头合成 CTP 的限速酶,组装成称为细胞丝的丝状结构。 Hippo 通路调节细胞增殖和凋亡。核苷酸代谢与 Hippo 通路的关系知之甚少。在这里,我们研究了 Hippo 通路对后滤泡细胞(PFC)中细胞丝的影响。我们发现 Hippo 通路失活与 PFC 中细胞丝长度和数量减少有关。在 CTPS 过表达期间,Hippo 突变的存在也会降低 PFC 中细胞丝的长度。此外,我们观察到敲低 CTPS 可减轻(Hippo)相关的过度增殖。总之,我们的结果表明 Hippo 通路与 PFC 中的核苷酸合成酶 CTPS 之间存在联系。