Expansion and innovation in auxin signaling: where do we grow from here?

ABSTRACTThe phytohormone auxin plays a role in almost all growth and developmental responses. The primary mechanism of auxin action involves the regulation of transcription via a core signaling pathway comprising proteins belonging to three classes: receptors, co-receptor/co-repressors and transcription factors. Recent studies have revealed that auxin signaling can be traced back at least as far as the transition to land. Moreover, studies in flowering plants have highlighted how expansion of the gene families encoding auxin components is tied to functional diversification. As we review here, these studies paint a picture of auxin signaling evolution as a driver of innovation.

Some New Methodological and Conceptual Aspects of the “Acid Growth Theory” for the Auxin Action in Maize (Zea mays L.) Coleoptile Segments: Do Acid- and Auxin-Induced Rapid Growth Differ in Their Mechanisms?

Two arguments against the “acid growth theory” of auxin-induced growth were re-examined. First, the lack of a correlation between the IAA-induced growth and medium acidification, which is mainly due to the cuticle, which is a barrier for proton diffusion. Second, acid- and the IAA-induced growth are additive processes, which means that acid and the IAA act via different mechanisms. Here, growth, medium pH, and membrane potential (in some experiments) were simultaneously measured using non-abraded and non-peeled segments but with the incubation medium having access to their lumen. Using such an approach significantly enhances both the IAA-induced growth and proton extrusion (similar to that of abraded segments). Staining the cuticle on the outer and inner epidermis of the coleoptile segments showed that the cuticle architecture differs on both sides of the segments. The dose-response curves for the IAA-induced growth and proton extrusion were bell-shaped with the maximum at 10−4 M over 10 h. The kinetics of the IAA-induced hyperpolarisation was similar to that of the rapid phase of the IAA-induced growth. It is also proposed that the K+/H+ co-transporters are involved in acid-induced growth and that the combined effect of the K+ channels and K+/ H+ co-transporters is responsible for the IAA-induced growth. These findings support the “acid growth theory” of auxin action.

Ethylene in the control of photoperiodic flower induction in Pharbitis nil Chois.

The content of endogenous ethylene in the seedlings of <em>Pharbitis nil</em> subjected to 16-hour long inductive night is low during the first half of a dark period, then it increases considerably in the second half of the night. Ethrel, the compound releasing ethylene, applied to the cotyledons of the seedlings, increases the amount of endogenous ethylene in them and at the same time inhibits the flowering, especially when ethrel was applied during the first half of an inductive night, when the content of endogenous ethylene in the seedlings is low. The auxin, inhibiting the flowering of <em>Pharbitis</em>, causes at the same time the increase in the production of endogenous ethylene. PCIB, an inhibitor of auxin action reverses the inhibiting influence of ethrel on flowering. On the other hand the combined application of ethrel and TIBA, the inhibitor of auxin polar transport, causes the increase of the flowering inhibition. CoCl₂, the inhibitor of ethylene biosynthesis, and AgNO₃, the inhibitor of ethylene action, reverse partly the inhibiting influence of auxin. It suggests that ethylene could take part in auxininhibition of flowering. The all obtained results seem to suggest the participation of ethylene in the control of the flower photoperiodic induction.