An ATP-responsive metabolic cassette comprised of inositol tris/tetrakisphosphate kinase 1 (ITPK1) and inositol pentakisphosphate 2-kinase (IPK1) buffers diphosphosphoinositol phosphate levels. Issue 14 (24th July 2020)

• Record Type: Journal Article
• Authors: Whitfield, Hayley; White, Gaye; Sprigg, Colleen; Riley, Andrew M.; Potter, Barry V.L.; Hemmings, Andrew M.; Brearley, Charles A.
• Is Part Of: Biochemical journal. Volume 477:Issue 14(2020)
• Page Start: 2621
• Page End: 2638
• Publication Date: 2020-07-24
• Subjects: diphosphoinositol phosphates -- energy charge -- IPK1 -- ITPK1 -- phosphate homeostasis; Biochemistry -- Periodicals; 572
• DOI: 10.1042/BCJ20200423
• Languages: English
• ISSNs: 0264-6021

Abstract

Abstract : Inositol polyphosphates are ubiquitous molecular signals in metazoans, as are their pyrophosphorylated derivatives that bear a so-called 'high-energy' phosphoanhydride bond. A structural rationale is provided for the ability of Arabidopsis inositol tris/tetrakisphosphate kinase 1 to discriminate between symmetric and enantiomeric substrates in the production of diverse symmetric and asymmetric myo -inositol phosphate and diphospho- myo -inositol phosphate (inositol pyrophosphate) products. Simple tools are applied to chromatographic resolution and detection of known and novel diphosphoinositol phosphates without resort to radiolabeling approaches. It is shown that inositol tris/tetrakisphosphate kinase 1 and inositol pentakisphosphate 2-kinase comprise a reversible metabolic cassette converting Ins(3, 4, 5, 6)P4 into 5-InsP7 and back in a nucleotide-dependent manner. Thus, inositol tris/tetrakisphosphate kinase 1 is a nexus of bioenergetics status and inositol polyphosphate/diphosphoinositol phosphate metabolism. As such, it commands a role in plants that evolution has assigned to a different class of enzyme in mammalian cells. The findings and the methods described will enable a full appraisal of the role of diphosphoinositol phosphates in plants and particularly the relative contribution of reversible inositol phosphate hydroxykinase and inositol phosphate phosphokinase activities to plant physiology.