Ethylene aplenty signals soil compaction: It's tough to drive a spade through compacted soil, and plant roots seem to have the same problem when growing in compacted ground. Pandey et al. found that the problem is not, however, one of physical resistance but rather inhibition of growth through a signaling pathway. The volatile plant hormone ethylene will diffuse through aerated soil, but compacted soil reduces such diffusion, increasing the concentration of ethylene near root tissues. The cellular signaling cascades triggered by too much ethylene stop root growth. Therefore, gaseous diffusion serves as a readout of soil compaction for plant roots growing in search of productive nutrition. Science , this issue p. 276

Rooting out the mechanism of asymmetry: Plant roots grow not in response to architectural blueprints but rather in search of scarce resources in the soil. Orosa-Puente et al. show why a new lateral root emerges on the damp side of a root rather than the dry side (see the Perspective by Giehl and von Wirén). The transcription factor ARF7 is found across the whole root but acquires a posttranslational modification on the dry side of the root, which represses its function. ARF7 on the damp side remains functional and is thus able to initiate the signaling cascade that leads to a new lateral root. Science , this issue p. 1407 ; see also p. 1358

Plant hormone auxin regulates several aspects of plant growth and development. Auxin is predominantly synthesized in the shoot apex and developing leaf primordia and from there it is transported to the target tissues e.g. roots. Auxin transport is polar in nature and is carrier-mediated. AUXIN1/LIKE-AUX1 (AUX1/LAX) family members are the major auxin influx carriers whereas PIN-FORMED (PIN) family and some members of the P-GLYCOPROTEIN/ATP-BINDING CASSETTE B4 (PGP/ABCB) family are major auxin efflux carriers. AUX1/LAX auxin influx carriers are multi-membrane spanning transmembrane proteins sharing similarity to amino acid permeases. Mutations in AUX1/LAX genes result in auxin related developmental defects and have been implicated in regulating key plant processes including root and lateral root development, root gravitropism, root hair development, vascular patterning, seed germination, apical hook formation, leaf morphogenesis, phyllotactic patterning, female gametophyte development and embryo development. Recently AUX1 has also been implicated in regulating plant responses to abiotic stresses. This review summarizes our current understanding of the developmental roles of AUX1/LAX gene family and will also briefly discuss the modelling approaches that are providing new insight into the role of auxin transport in plant development.

Phosphate (P) is an essential macronutrient for plant growth. Roots employ adaptive mechanisms to forage for P in soil. Root hair elongation is particularly important since P is immobile. Here we report that auxin plays a critical role promoting root hair growth in Arabidopsis in response to low external P. Mutants disrupting auxin synthesis (taa1) and transport (aux1) attenuate the low P root hair response. Conversely, targeting AUX1 expression in lateral root cap and epidermal cells rescues this low P response in aux1. Hence auxin transport from the root apex to differentiation zone promotes auxin-dependent hair response to low P. Low external P results in induction of root hair expressed auxin-inducible transcription factors ARF19, RSL2, and RSL4. Mutants lacking these genes disrupt the low P root hair response. We conclude auxin synthesis, transport and response pathway components play critical roles regulating this low P root adaptive response.

Significance: Understanding how hormones like auxin control plant growth and development has fascinated scientists since Darwin. The past two decades have seen breakthroughs in elucidating the molecular basis of auxin transport, perception, and response, but little is known about how auxin is metabolized or its homeostasis is controlled. We report that the DIOXYGENASE FOR AUXIN OXIDATION 1 ( AtDAO1 ) enzyme represents the major pathway for auxin oxidation in Arabidopsis . Disrupting AtDAO1 function elevates levels of auxin conjugates between ∼50- and 280-fold, but auxin levels remain close to the WT, helping explain why mutant phenotypes are relatively weak. We conclude that AtDAO1 and auxin conjugation pathways play highly redundant roles and reveal a level of regulation of auxin abundance in plants.