Signals can be perceived and amplified at the cell membrane by receptors coupled to the production of a variety of second messengers, including inositol 1,4,5-trisphosphate (IP 3 ). We previously have identified 15 putative inositol 5-phosphatases (5PTases) from Arabidopsis and shown that At5PTase1 can hydrolyze IP 3 . To determine whether At5PTase1 can terminate IP 3 -mediated signaling, we analyzed transgenic plants ectopically expressing At5PTase1. Stomata from leaves of At5PTase1 transgenic plants were abscisic acid (ABA) and light insensitive, and ABA induction of genes was delayed. Quantification of IP 3 in plants exposed to ABA indicated that ABA induced two IP 3 increases in wild-type plants. Both of these IP 3 increases were reduced in At5PTase1 transgenic plants, indicating that IP 3 may be necessary for stomatal closure and temporal control of ABA-induced gene expression. To determine if ABA could induce expression of At5PTase1, we examined RNA and protein levels of At5PTase1 in wild-type plants exposed to ABA. Our results indicate that At5PTase1 is up-regulated in response to ABA. This is consistent with At5PTase1 acting as a signal terminator of ABA signaling.The ability to respond to a variety of biotic and abiotic signals is crucial to plants. Signals outside the cell can be perceived and amplified at the cell membrane by receptors linked to a variety of signaling pathways, including the inositol 1,4,5-trisphosphate (IP 3 ) pathway (Stevenson et al., 2000; Taylor and Thorn, 2001). In this pathway, signals activate phospholipase C (PLC), which catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to form diacylglycerol and IP 3 . IP 3 then binds to intracellular receptors, triggering the release of Ca 2ϩ from intracellular stores into the cytosol (Berridge, 1993).In plants, there is evidence that signals such as light (Shacklock et al., 1992), gravity (Perera et al., 1999(Perera et al., , 2001, and abscisic acid (ABA; Wu et al., 1997; Sanchez and Chua, 2001) are relayed via IP 3 signaling. Most of the information on IP 3 signaling has arisen from studies utilizing ABA. The most notable affect of ABA on plants is its ability to induce stomatal closure (Allen et al., 2001). When open, stomatal pores allow the influx of CO 2 and water vapor to move outward, driving the transpirational process. ABA is thought to trigger stomatal closure by inducing cytosolic Ca 2ϩ increases, which, in turn inhibit plasma membrane H ϩ -ATPases and inwardrectifying K ϩ channels. Subsequent activation of outward-rectifying K ϩ channels allows for ion efflux from the guard cell and a decrease in guard cell turgor, resulting in stomatal closure (Blatt et al., 1990;Lemtiri-Chlieh and MacRobbie, 1994; Schroeder et al., 2001a).One key component in the mechanism of stomatal closure is an initial increase in cytosolic Ca 2ϩ concentration that occurs within minutes of ABA exposure (McAinsh et al., 2000;Allen et al., 2001; Webb et al., 2001). This rapid increase in Ca 2ϩ is preceded by an increase in IP 3 (Lee et a...