| Literature DB >> 33113373 |
Emma Bondy-Chorney1, Iryna Abramchuk2, Rawan Nasser3, Charlotte Holinier3, Alix Denoncourt3, Kanchi Baijal3, Liam McCarthy3, Mireille Khacho2, Mathieu Lavallée-Adam2, Michael Downey4.
Abstract
Polyphosphates (polyPs) are long chains of inorganic phosphates linked by phosphoanhydride bonds. They are found in all kingdoms of life, playing roles in cell growth, infection, and blood coagulation. Unlike in bacteria and lower eukaryotes, the mammalian enzymes responsible for polyP metabolism are largely unexplored. We use RNA sequencing (RNA-seq) and mass spectrometry to define a broad impact of polyP produced inside of mammalian cells via ectopic expression of the E. coli polyP synthetase PPK. We find that multiple cellular compartments can support accumulation of polyP to high levels. Overproduction of polyP is associated with reprogramming of both the transcriptome and proteome, including activation of the ERK1/2-EGR1 signaling axis. Finally, fractionation analysis shows that polyP accumulation results in relocalization of nuclear/cytoskeleton proteins, including targets of non-enzymatic lysine polyphosphorylation. Our work demonstrates that internally produced polyP can activate diverse signaling pathways in human cells.Entities:
Keywords: ERK1/2; PPK; RNA-seq; mTOR; polyP; polyphosphate; polyphosphorylation; proteomics
Year: 2020 PMID: 33113373 DOI: 10.1016/j.celrep.2020.108318
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423