<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Gu C</dc:creator>
  <dc:creator>Nguyen HN</dc:creator>
  <dc:creator>Hofer A</dc:creator>
  <dc:creator>Jessen HJ</dc:creator>
  <dc:creator>Dai X</dc:creator>
  <dc:creator>Wang H</dc:creator>
  <dc:creator>Shears SB</dc:creator>
  <dc:date>2017</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Proteins responsible for Pi homeostasis are critical for all life. In Saccharomyces cerevisiae, extracellular [Pi] is "sensed" by the inositol-hexakisphosphate kinase (IP6K) that synthesizes the intracellular inositol pyrophosphate 5-diphosphoinositol 1,2,3,4,6-pentakisphosphate (5-InsP7) as follows: during a period of Pi starvation, there is a decline in cellular [ATP]; the unusually low affinity of IP6Ks for ATP compels 5-InsP7 levels to fall in parallel (Azevedo, C., and Saiardi, A. (2017) Trends. Biochem. Sci. 42, 219-231. Hitherto, such Pi sensing has not been documented in metazoans. Here, using a human intestinal epithelial cell line (HCT116), we show that levels of both 5-InsP7 and ATP decrease upon [Pi] starvation and subsequently recover during Pi replenishment. However, a separate inositol pyrophosphate, 1,5-bisdiphosphoinositol 2,3,4,6-tetrakisphosphate (InsP8), reacts more dramatically (i.e. with a wider dynamic range and greater sensitivity). To understand this novel InsP8 response, we characterized kinetic properties of the bifunctional 5-InsP7 kinase/InsP8 phosphatase activities of full-length diphosphoinositol pentakisphosphate kinases (PPIP5Ks). These data fulfil previously published criteria for any bifunctional kinase/phosphatase to exhibit concentration robustness, permitting levels of the kinase product (InsP8 in this case) to fluctuate independently of varying precursor (i.e. 5-InsP7) pool size. Moreover, we report that InsP8 phosphatase activities of PPIP5Ks are strongly inhibited by Pi (40-90% within the 0-1 mm range). For PPIP5K2, Pi sensing by InsP8 is amplified by a 2-fold activation of 5-InsP7 kinase activity by Pi within the 0-5 mm range. Overall, our data reveal mechanisms that can contribute to specificity in inositol pyrophosphate signaling, regulating InsP8 turnover independently of 5-InsP7, in response to fluctuations in extracellular supply of a key nutrient.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/88390</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.M116.765743</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/28126903</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>The Journal of biological chemistry. - 2017</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">inositol phosphate</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">metabolism</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">phosphatase</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">signal transduction</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">signaling</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Acid Anhydride Hydrolases</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Adenosine Triphosphate</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">HCT116 Cells</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">HEK293 Cells</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Homeostasis</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Inositol Phosphates</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Phosphotransferases (Phosphate Group Acceptor)</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Signal Transduction</dc:subject>
  <dc:title xmlns:ns15="xml" ns15:lang="en">The Significance of the Bifunctional Kinase/Phosphatase Activities of Diphosphoinositol Pentakisphosphate Kinases (PPIP5Ks) for Coupling Inositol Pyrophosphate Cell Signaling to Cellular Phosphate Homeostasis.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
