ABSTRACrAs a part of our effort to study the mode of action of abscisic acid (ABA) and its metabolites during seed germination, we have investigated the regulaton of ABA metabolism in barley (Hordeum vulgare) aurone layers and a few other plant tissues. The rate of conversion of pHIABA to I3Hlphaseic acid (PA) the first stable metabolite of ABA, is enhanced by 2-to 5-fold in barley aleurone layers when the tissue is pretreated with ABA. However, the conversion of I3HIPA to 1HI dihydrophaseic acid (DPA), the next metabolite after PA, is not enhanced by pretreatment with either ABA or PA. The ABA enhancement of its own metabolism in barley aleurone layers is detectable with a pretreatment ofABA rai from 109 to 10 molar. This apparent self-induction of ABA conversion to PA can be observed after the barley aleurone layers have been treated with 10 molar ABA for as short as 2 hours, and is inhibited by the transcription inhibitor, cordycepin (3'-deoxyadenosine), or the translation inhibitor, cycloheximide. The self-induction of ABA conversion to PA also occurs in wheat aleurone layers, but not in other plant tissues that have been investipted, including corm root tips, barley embryos, barley, and soybean leaf discs. It is probably a phenomenon unique to the aleurone layers of some cereal grains. In view of the recent observations that ABA is able to induce new proteins in barley aleurone layers, we suggest that some of these ABA-induced proteins are involved in the conversion from ABA to PA in this tissue.It has been well documented that ABA exerts regulatory roles in many physiological processes such as stomatal closure, bud dormancy, seed dormancy, seed development, and germination (for a review, see 17). The mode of ABA action during seed germination has been studied in many systems including cotton embryos (4, 12), wheat embryos (1), and barley aleurone layers (2,8,10,13,18). In barley aleurone layers, ABA inhibits the GA3-enhanced synthesis of a-amylase (2, 10). This inhibition is not due to the direct competition between GA and ABA for a common site of action because high concentrations of GA do not completely overcome the effect of ABA (2,13). Similar to what was reported in cotton and wheat embryos (1, 12), the effect of ABA in barley aleurone layers can be prevented by transcription inhibitors (e.g. cordycepin) indicating that the action of this hormone is dependent on the continuous synthesis of RNA and/or proteins (10). More that ABA induces the synthesis of several new proteins in both cotton embryos (4) and barley aleurone layers (8, 9, 11, 15 MATERIALS AND METHODS Chemicals. Cis, trans, and mixed isomers of ABA were purchased from Sigma Chemical Co. DL-cis,trans-[3HJABA (10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20) Ci/mmol) and DL-cis,trans-`'4C]ABA (11.9 mCi/mmol) were obtained from Amersham. The purity of the labeled ABA was greater than 98% as analyzed by TLC. Phaseic acid and DPA were purified according to Sharkey and Raschke (16)