Impaired manganese metabolism causes mitotic misregulation

Abstract

Manganese is an essential trace element, whose intracellular levels need to be carefully regulated. Mn2+ acts as a cofactor for many enzymes and excess of Mn2+ is toxic. Alterations in Mn2+homeostasis affect metabolic functions and mutations in the human Mn2+/Ca 2+ transporter ATP2C1 have been linked to Hailey-Hailey disease. By deletion of the yeast orthologuePMR1 we have studied the impact of Mn 2+ on cell cycle progression and show that an excess of cytosolicMn2+ alters S-phase transit, induces transcriptional up-regulation of cell cycle regulators, bypasses the need for S-phase cell cycle checkpoints and predisposes to genomic instability. On the other hand, we find that depletion of the Golgi Mn2+ pool requires a functional morphology checkpoint to avoid the formation of polyploid cells. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.