Abstract

Auxin plays a major role in a variety of processes involved in plant developmental patterning and its adaptation to environmental conditions. Therefore, an important question is how specificity in auxin signalling is achieved, that is, how a single signalling molecule can carry so many different types of information. In recent years, many studies on auxin specificity have been published, unravelling increasingly more details on differential auxin sensitivity, expression domains and downstream partners of the auxin receptors (transport inhibitor response 1 (TIR1) and other auxin signaling F-box proteins (AFB)), transcriptional repressors that are degraded in response to auxin (AUX/IAA) and downstream auxin response factors (ARF) that together constitute the plant’s major auxin response pathways. These data are critical to explain how, in the same cells, different auxin levels may trigger different responses, as well as how in different spatial or temporal contexts similar auxin signals converge to different responses. However, these insights do not yet answer more complex questions regarding auxin specificity. As an example, they leave open the question of how similar sized auxin changes at similar locations result in different responses depending on the duration and spatial extent of the fluctuation in auxin levels. Similarly, it leaves unanswered how, in the case of certain tropisms, small differences in signal strength at both sides of a plant organ are converted into an instructive auxin asymmetry that enables a robust tropic response. Finally, it does not explain how, in certain cases, substantially different auxin levels become translated into similar cellular responses, while in other cases similar auxin levels, even when combined with similar auxin response machinery, may trigger different responses. In this review, we illustrate how considering the regulatory networks and contexts in which auxin signalling takes place helps answer these types of fundamental questions.

Highlights

  • The plant hormone auxin plays an important role in a wide range of developmental processes [1] as well as in a wide range of adaptive responses to environmental conditions [2,3]

  • The consecutive activation of the IAA28/ARF5,6,7,8,19, the IAA14/ARF7,19 and the IAA12/ARF5 auxin response modules involved in lateral root formation [27] may be related to an increase in auxin levels generated by the currently active module as well as feedbacks between the different modules [28,29]

  • In the plant root, a gradient of auxin controls developmental zonation, with highest auxin levels corresponding to the quiescent center (QC) and surrounding stem cell niche (SCN), and gradually declining levels occurring throughout the rest of the meristem, elongation and differentiation zones [5,6,32,33]

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Summary

Introduction

The plant hormone auxin plays an important role in a wide range of developmental processes [1] as well as in a wide range of adaptive responses to environmental conditions [2,3]. In most tropisms, the oriented growth of plant organs towards or away from a particular signal is guided by an instructive auxin asymmetry [13,14,15] and remodeling of overall plant root architecture in response to environmental conditions involves changes in auxin distribution patterns [16,17]. The insights on differential auxin sensitivity, expression domains, and downstream targets of different TIR/AFB, AUX/IAA and ARF types are insufficient to answer more complicated questions on auxin specificity.

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