The essential metabolic enzyme CTP synthase catalyses CTP formation and has been demonstrated to form large, evolutionarily conserved intracellular filaments, termed cytoophidia (meaning cellular serpents in Greek). The exact functional role of cytoophidia, or how formation and maintenance is regulated remains unanswered. By monitoring cytoophidium formation in a GFP tagged CTP synthase background in Schizsaccharomyces pombe, we have discovered that the TOR (target of rapamycin) kinase pathway regulates cytoophidium formation. The TOR pathway is highly conserved and is essential for regulation of cell growth and response to nutrient deprivation. We show that the TOR signalling cascade is involved in cytoophidium assembly. Moreover, this relationship is specific to the TORC2 complex. This study connects cytoophidium assembly and the TORC2 complex which is potentially relevant considering the increasing evidence implicating these two major pathways in cancer development.