2008
DOI: 10.1073/pnas.0807814105
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Mechanical induction of lateral root initiation in Arabidopsis thaliana

Abstract: Lateral roots are initiated postembryonically in response to environmental cues, enabling plants to explore efficiently their underground environment. However, the mechanisms by which the environment determines the position of lateral root formation are unknown. In this study, we demonstrate that in Arabidopsis thaliana lateral root initiation can be induced mechanically by either gravitropic curvature or by the transient bending of a root by hand. The plant hormone auxin accumulates at the site of lateral roo… Show more

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Cited by 263 publications
(258 citation statements)
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“…Molecular studies showed that auxin and its polar transport are the central regulators of lateral root formation. It has been reported that auxin-dependent nuclear signaling is necessary for lateral root formation (Ditengou et al, 2008). Optimum rooting response using IBA and NAA has been reported for several other medicinal plants including Syzygium francissi (Shatnawi et al, 2004), pear (Shatnawi et al, 2007), Achillea millefolium (Shatnawi, 2013), and Stevia rebaudiana (Zayova et al, 2013).…”
Section: In Vitro Root Formation and Acclimatizationmentioning
confidence: 99%
“…Molecular studies showed that auxin and its polar transport are the central regulators of lateral root formation. It has been reported that auxin-dependent nuclear signaling is necessary for lateral root formation (Ditengou et al, 2008). Optimum rooting response using IBA and NAA has been reported for several other medicinal plants including Syzygium francissi (Shatnawi et al, 2004), pear (Shatnawi et al, 2007), Achillea millefolium (Shatnawi, 2013), and Stevia rebaudiana (Zayova et al, 2013).…”
Section: In Vitro Root Formation and Acclimatizationmentioning
confidence: 99%
“…The seedlings were then incubated in 1 mM 5-bromo-4-chloro-3-indolyl β-D-glucuronide cyclohexylammonium salt, 100 mM potasium phosphate buffer (pH 7.0), 1 mM EDTA, 1 mM potassium hexacyanoferrate, 1 mM potassium hexacyanoferrate, and 0.3% Triton X-100 overnight at 37°C. For visualization of blue staining the chlorophyll was removed by incubation in 70% ethanol (34).…”
Section: Methodsmentioning
confidence: 99%
“…Immunolocalization of PIN1 was performed using an affinity-purified rabbit anti-PIN1 antibody as described by Gälweiler et al (1998). Dilutions of primary anti-PIN2 guinea pig antibody (Ditengou et al, 2008) was 1:600 and for the anti-PM H + -ATPase rabbit antibody (Langhans et al, 2001; Agrisera AS07 260) 1:1000. As secondary antibodies, ALEXA Fluor 488 goat anti-guinea pig (Invitrogen) and ALEXA Fluor 555 goat anti-rabbit (Invitrogen) diluted to 1:600 were used.…”
Section: Histochemical Gus and Starch Staining And Immunolocalizationmentioning
confidence: 99%