z-logo
open-access-imgOpen Access
An Arabidopsis Inositol 5-Phosphatase Gain-of-Function Alters Abscisic Acid Signaling
Author(s) -
Ryan N. Burnette
Publication year - 2003
Publication title -
plant physiology
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.102.019000
Subject(s) - abscisic acid , arabidopsis , inositol , second messenger system , phosphatase , biology , signal transduction , microbiology and biotechnology , transgene , inositol phosphate , gene , receptor , biochemistry , phosphorylation , mutant
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 (IP3). We previously have identified 15 putative inositol 5-phosphatases (5PTases) from Arabidopsis and shown that At5PTase1 can hydrolyze IP3. To determine whether At5PTase1 can terminate IP3-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 IP3 in plants exposed to ABA indicated that ABA induced two IP3 increases in wild-type plants. Both of these IP3 increases were reduced in At5PTase1 transgenic plants, indicating that IP3 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 content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom