ArticlePlant & cell physiology2018
Asymmetric Auxin Distribution is Not Required to Establish Root Phototropism in Arabidopsis.
Article in Plant & cell physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed, 15 citations in OpenAlex.
- Physiological and transcriptomic assessment of Arabidopsis identifies two distinct gravity signaling systems.Plant physiology · 2026Article
- Integrated transcriptome and endogenous hormone analysis provides new insights into callus proliferation in Osmanthus fragrans.Scientific reports · 2022Article
- Root growth direction in simulated microgravity is modulated by a light avoidance mechanism mediated by flavonols.Physiologia plantarum · 2022Article
- Root electrotropism in Arabidopsis does not depend on auxin distribution but requires cytokinin biosynthesis.Plant physiology · 2022Article
- Root dynamic growth strategies in response to salinity.Plant, cell & environment · 2022Review
- Modeling Auxin Signaling in Roots: Auxin Computations.Cold Spring Harbor perspectives in biology · 2022Review
- Molecular mechanisms mediating root hydrotropism: what we have observed since the rediscovery of hydrotropism.Journal of plant research · 2020Review
- Root Tropisms: Investigations on Earth and in Space to Unravel Plant Growth Direction.Frontiers in plant science · 2019Review
Corrections and comments
- Erratum issuedErratum.2018
Authors and funding
8 authors at 6 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An asymmetric auxin distribution pattern is assumed to underlie the tropic responses of seed plants. It is unclear, however, whether this pattern is required for root negative phototropism. We here demonstrate that asymmetric auxin distribution is not required to establish root phototropism in Arabidopsis. Our detailed analyses of auxin reporter genes indicate that auxin accumulates on the irradiated side of roots in response to an incidental gravitropic stimulus caused by phototropic bending. Further, an agravitropic mutant showed a suppression of this accumulation with an enhancement of the phototropic response. In this context, our pharmacological and genetic analyses revealed that both polar auxin transport and auxin biosynthesis are critical for the establishment of root gravitropism, but not for root phototropism, and that defects in these processes actually enhance phototropic responses in roots. The auxin response factor double mutant arf7 arf19 and the auxin receptor mutant tir1 showed a slight reduction in phototropic curvatures in roots, suggesting that the transcriptional regulation by some specific ARF proteins and their regulators is at least partly involved in root phototropism. However, the auxin antagonist PEO-IAA [α-(phenylethyl-2-one)-indole-3-acetic acid] suppressed root gravitropism and enhanced root phototropism, suggesting that the TIR1/AFB auxin receptors and ARF transcriptional factors play minor roles in root phototropism. Taken together, we conclude from our current data that the phototropic response in Arabidopsis roots is induced by an unknown mechanism that does not require asymmetric auxin distribution and that the Cholodny-Went hypothesis probably does not apply to root phototropism.
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