The fission yeast Greatwall–Endosulfine pathway is required for proper quiescence/G0 phase entry and maintenance

• Published in: Genes to cells : devoted to molecular & cellular mechanisms 2019-02, Vol.24 (2), p.172-186
• Main Authors: Aono, Soma, Haruna, Yui, Watanabe, Yo‐hei, Mochida, Satoru, Takeda, Kojiro
• Format: Article
• Language: English
• Subjects: Alanine; Cell proliferation; Cellular quiescence; Clonal deletion; Endosulfine; G0 phase; Gene deletion; Genetic analysis; Greatwall kinase; Kinases; Mitosis; Phenotypes; PP2A; Protein kinase; Protein phosphatase; Proteins; S. pombe; Serine; Yeast
• ISSN: 1356-9597; 1365-2443
• DOI: 10.1111/gtc.12665

Cell proliferation and cellular quiescence/G0 phase must be regulated in response to intra‐/extracellular environments, and such regulation is achieved by the orchestration of protein kinases and protein phosphatases. Here, we investigated fission yeast potential orthologs (Cek1, Ppk18 and Ppk31) of the metazoan Greatwall kinase (Gwl), which inhibits type‐2A protein phosphatase with B55 subunit (PP2AB55) by phosphorylating and activating the PP2AB55 inhibitors, α‐endosulfine/ARPP‐19 (Ensa/ARPP‐19). Gwl and Ensa/ARPP‐19 regulate mitosis; however, we found Ppk18, Cek1 and Mug134/Igo1, the counterpart of Ensa/ARPP‐19, are not essential for normal mitosis but regulate nitrogen starvation (−N)‐induced proper G0 entry and maintenance. Genetic and biochemical analyses indicated that the conserved Gwl site (serine 64) was phosphorylated in the G0 phase in a Ppk18‐dependent manner, and the phosphorylated Mug134/Igo1 inhibited PP2AB55 in vitro. The alanine substitution of the serine 64 caused defects in G0 entry and maintenance as well as the mug134/igo1+ deletion. These results indicate that PP2AB55 activity must be regulated properly to establish the G0 phase. Consistently, simultaneous deletion of the B55 gene with mug134/igo1+ partially rescued the Mug134/Igo1 mutant phenotype. We suggest that in fission yeast, PP2AB55 regulation by the Ppk18‐Mug134/Igo1 pathway is required for G0 entry and establishment of robust viability during the G0 phase. Cell cycle progression and cellular quiescence/G0 phase must be regulated in response to intracellular and extracellular environments, and such regulation is achieved by the orchestration of protein kinases and protein phosphatases. We investigated fission yeast orthologs of Greatwall kinase (Gwl) and ɑ‐endosulfine (Ensa). The Gwl‐Ensa pathway is indispensable for establishment and maintenance of G0 phase through regulating activity of PP2AB55 in the fission yeast.