4.8 Article

Zea mays Annexins Modulate Cytosolic Free Ca2+ and Generate a Ca2+-Permeable Conductance

期刊

PLANT CELL
卷 21, 期 2, 页码 479-493

出版社

AMER SOC PLANT BIOLOGISTS
DOI: 10.1105/tpc.108.059550

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资金

  1. Biotechnology and Biological Science Research Council
  2. Isaac Newton Trust
  3. Cambridge Overseas Trusts
  4. University of Cambridge Department of Plant Sciences Research Fund
  5. BBSRC [BB/D017904/1] Funding Source: UKRI
  6. NERC [MBA010001] Funding Source: UKRI
  7. Biotechnology and Biological Sciences Research Council [REI20579, BB/C505232/1, BB/D017904/1] Funding Source: researchfish
  8. Natural Environment Research Council [MBA010001] Funding Source: researchfish

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Regulation of reactive oxygen species and cytosolic free calcium ([Ca2+](cyt)) is central to plant function. Annexins are small proteins capable of Ca2+-dependent membrane binding or membrane insertion. They possess structural motifs that could support both peroxidase activity and calcium transport. Here, a Zea mays annexin preparation caused increases in [Ca2+] cyt when added to protoplasts of Arabidopsis thaliana roots expressing aequorin. The pharmacological profile was consistent with annexin activation (at the extracellular plasma membrane face) of Arabidopsis Ca2+-permeable nonselective cation channels. Secreted annexins could therefore modulate Ca2+ influx. As maize annexins occur in the cytosol and plasma membrane, they were incorporated at the intracellular face of lipid bilayers designed to mimic the plasma membrane. Here, they generated an instantaneously activating Ca2+-permeable conductance at mildly acidic pH that was sensitive to verapamil and Gd3+ and had a Ca2+-to-K+ permeability ratio of 0.36. These results suggest that cytosolic annexins create a Ca2+ influx pathway directly, particularly during stress responses involving acidosis. A maize annexin preparation also demonstrated in vitro peroxidase activity that appeared independent of heme association. In conclusion, this study has demonstrated that plant annexins create Ca2+-permeable transport pathways, regulate [Ca2+] cyt, and may function as peroxidases in vitro.

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