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This finally leads to the observed Ca2+ transient and it should be emphasized that a tight regulation of Ca2+ efflux is as equally important for Ca2+ signaling as the more intensively studied influx mechanisms. Extrusion of calcium is achieved by P-type calcium-ATPases and by Ca2+/H+ antiporter systems. While pumps mediate high-affinity low-turnover Ca2+ export, antiporter provoke low-affinity high-capacity export. Therefore, antiporter reduce the Ca2+ cytoplasmic level to a few micromolar after signal mediated influx of Ca2+, while calcium-ATPases further lessen the cytoplasmic Ca2+ concentration to the resting level and maintain the Ca2+ homeostasis (Bush 1993; Hirschi 1999).
2001; Shigaki et al. 2006) that contribute to the regulation of Ca2+ (Catala et al. 2003; Cheng et al. 2003; Zhao et al. 2008). In addition, five cation calcium exchanger (CCX) proteins (also termed CAX7-11), related to K+ dependent Na+/Ca2+ antiporters are encoded in the Arabidopsis genome (Shigaki et al. 2006). Moreover, four putative antiporters are encoded in the genome of Arabidopsis, which exhibit EF hand Ca2+ binding motifs suggesting that they are directly regulated by Ca2+ (Shigaki et al.
While NpCaM1 is upregulated by wind and cold, the expression of NpCaM2 is unaffected (van Der Luit et al. 1999). In Arabidopsis, one CaM and different CMLs are induced by touch (Braam et al. 1997). Additionally, CML expression can be tissue specific and can be modulated by stress, hormones and light (McCormack et al. 2005; Magnan et al. 2008). Post-transcriptional regulation of protein stability by methylation or phosphorylation could also play an important role (Oh and Roberts 1990; Leclerc et al.