MAPKs Influence Pollen Tube Growth by Controlling the Formation of Phosphatidylinositol 4, 5-Bisphosphate in an Apical Plasma Membrane Domain. Issue 12 (22nd November 2017)
- Record Type:
- Journal Article
- Title:
- MAPKs Influence Pollen Tube Growth by Controlling the Formation of Phosphatidylinositol 4, 5-Bisphosphate in an Apical Plasma Membrane Domain. Issue 12 (22nd November 2017)
- Main Title:
- MAPKs Influence Pollen Tube Growth by Controlling the Formation of Phosphatidylinositol 4, 5-Bisphosphate in an Apical Plasma Membrane Domain
- Authors:
- Hempel, Franziska
Stenzel, Irene
Heilmann, Mareike
Krishnamoorthy, Praveen
Menzel, Wilhelm
Golbik, Ralph
Helm, Stefan
Dobritzsch, Dirk
Baginsky, Sacha
Lee, Justin
Hoehenwarter, Wolfgang
Heilmann, Ingo - Abstract:
- Abstract : The production of regulatory membrane phospholipids required for polar tip growth of pollen tubes is controlled by mitogen-activated protein kinases. Abstract: An apical plasma membrane domain enriched in the regulatory phospholipid phosphatidylinositol 4, 5-bisphosphate [PtdIns(4, 5)P2 ] is critical for polar tip growth of pollen tubes. How the biosynthesis of PtdIns(4, 5)P2 by phosphatidylinositol 4-phosphate 5-kinases (PI4P 5-kinases) is controlled by upstream signaling is currently unknown. The pollen-expressed PI4P 5-kinase PIP5K6 is required for clathrin-mediated endocytosis and polar tip growth in pollen tubes. Here, we identify PIP5K6 as a target of the pollen-expressed mitogen-activated protein kinase MPK6 and characterize the regulatory effects. Based on an untargeted mass spectrometry approach, phosphorylation of purified recombinant PIP5K6 by pollen tube extracts could be attributed to MPK6. Recombinant MPK6 phosphorylated residues T590 and T597 in the variable insert of the catalytic domain of PIP5K6, and this modification inhibited PIP5K6 activity in vitro. PIP5K6 interacted with MPK6 in yeast two-hybrid tests, immuno-pull-down assays, and by bimolecular fluorescence complementation at the apical plasma membrane of pollen tubes. In vivo, MPK6 expression resulted in reduced plasma membrane association of a fluorescent PtdIns(4, 5)P2 reporter and decreased endocytosis without impairing membrane association of PIP5K6. Effects of PIP5K6 expression onAbstract : The production of regulatory membrane phospholipids required for polar tip growth of pollen tubes is controlled by mitogen-activated protein kinases. Abstract: An apical plasma membrane domain enriched in the regulatory phospholipid phosphatidylinositol 4, 5-bisphosphate [PtdIns(4, 5)P2 ] is critical for polar tip growth of pollen tubes. How the biosynthesis of PtdIns(4, 5)P2 by phosphatidylinositol 4-phosphate 5-kinases (PI4P 5-kinases) is controlled by upstream signaling is currently unknown. The pollen-expressed PI4P 5-kinase PIP5K6 is required for clathrin-mediated endocytosis and polar tip growth in pollen tubes. Here, we identify PIP5K6 as a target of the pollen-expressed mitogen-activated protein kinase MPK6 and characterize the regulatory effects. Based on an untargeted mass spectrometry approach, phosphorylation of purified recombinant PIP5K6 by pollen tube extracts could be attributed to MPK6. Recombinant MPK6 phosphorylated residues T590 and T597 in the variable insert of the catalytic domain of PIP5K6, and this modification inhibited PIP5K6 activity in vitro. PIP5K6 interacted with MPK6 in yeast two-hybrid tests, immuno-pull-down assays, and by bimolecular fluorescence complementation at the apical plasma membrane of pollen tubes. In vivo, MPK6 expression resulted in reduced plasma membrane association of a fluorescent PtdIns(4, 5)P2 reporter and decreased endocytosis without impairing membrane association of PIP5K6. Effects of PIP5K6 expression on pollen tube growth and cell morphology were attenuated by coexpression of MPK6 in a phosphosite-dependent manner. Our data indicate that MPK6 controls PtdIns(4, 5)P2 production and membrane trafficking in pollen tubes, possibly contributing to directional growth. … (more)
- Is Part Of:
- The Plant Cell. Volume 29:Issue 12(2017)
- Journal:
- The Plant Cell
- Issue:
- Volume 29:Issue 12(2017)
- Issue Display:
- Volume 29, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 29
- Issue:
- 12
- Issue Sort Value:
- 2017-0029-0012-0000
- Page Start:
- 3030
- Page End:
- 3050
- Publication Date:
- 2017-11-22
- Journal URLs:
- http://www.oxfordjournals.org/ ↗
- DOI:
- 10.1105/tpc.17.00543 ↗
- Languages:
- English
- ISSNs:
- 1040-4651
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 16318.xml