BackgroundPlant root growth and development is highly plastic and can adapt to many environmental conditions. Sugar signaling has been shown to affect root growth and development by interacting with phytohormones such as gibberellins, cytokinin and abscisic acid. Auxin signaling and transport has been earlier shown to be controlling plant root length, number of lateral roots, root hair and root growth direction.Principal FindingsIncreasing concentration of glucose not only controls root length, root hair and number of lateral roots but can also modulate root growth direction. Since root growth and development is also controlled by auxin, whole genome transcript profiling was done to find out the extent of interaction between glucose and auxin response pathways. Glucose alone could transcriptionally regulate 376 (62%) genes out of 604 genes affected by IAA. Presence of glucose could also modulate the extent of regulation 2 fold or more of almost 63% genes induced or repressed by IAA. Interestingly, glucose could affect induction or repression of IAA affected genes (35%) even if glucose alone had no significant effect on the transcription of these genes itself. Glucose could affect auxin biosynthetic YUCCA genes family members, auxin transporter PIN proteins, receptor TIR1 and members of a number of gene families including AUX/IAA, GH3 and SAUR involved in auxin signaling. Arabidopsis auxin receptor tir1 and response mutants, axr2, axr3 and slr1 not only display a defect in glucose induced change in root length, root hair elongation and lateral root production but also accentuate glucose induced increase in root growth randomization from vertical suggesting glucose effects on plant root growth and development are mediated by auxin signaling components.ConclusionOur findings implicate an important role of the glucose interacting with auxin signaling and transport machinery to control seedling root growth and development in changing nutrient conditions.

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We present optical photometric and spectroscopic observations of supernova 2013ej. It is one of the brightest type II supernovae exploded in a nearby (∼ 10 Mpc) galaxy NGC 628. The light curve characteristics are similar to type II SNe, but with a relatively shorter (∼ 85 day) and steeper (∼ 1.7 mag (100 d) −1 in V ) plateau phase. The SN shows a large drop of 2.4 mag in V band brightness during plateau to nebular transition. The absolute ultraviolet (UV) light curves are identical to SN 2012aw, showing a similar UV plateau trend extending up to 85 days. The radioactive 56 Ni mass estimated from the tail luminosity is 0.02M ⊙ which is significantly lower than typical type IIP SNe. The characteristics of spectral features and evolution of line velocities indicate that SN 2013ej is a type II event. However, light curve characteristics and some spectroscopic features provide strong support in classifying it as a type IIL event. A detailed synow modelling of spectra indicates the presence of some high velocity components in Hα and Hβ profiles, implying possible ejecta-CSM interaction. The nebular phase spectrum shows an unusual notch in the Hα emission which may indicate bipolar distribution of 56 Ni. Modelling of the bolometric light curve yields a progenitor mass of ∼ 14M ⊙ and a radius of ∼ 450R ⊙ , with a total explosion energy of ∼ 2.3 × 10 51 erg.

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Directional growth of roots is a complex process that is modulated by various environmental signals. This work shows that presence of glucose (Glc) in the medium also extensively modulated seedling root growth direction. Glc modulation of root growth direction was dramatically enhanced by simultaneous brassinosteroid (BR) application. Glc enhanced BR receptor BRASSINOSTEROID INSENSITIVE1 (BRI1) endocytosis from plasma membrane to early endosomes. Glc-induced root deviation was highly enhanced in a PP2A-defective mutant, roots curl in naphthyl phthalamic acid 1-1 (rcn1-1) suggesting that there is a role of phosphatase in Glc-induced root-growth deviation. RCN1, therefore, acted as a link between Glc and the BR-signalling pathway. Polar auxin transport worked further downstream to BR in controlling Glc-induced root deviation response. Glc also affected other root directional responses such as root waving and coiling leading to altered root architecture. High light intensity mimicked the Glc-induced changes in root architecture that were highly reduced in Glc-signalling mutants. Thus, under natural environmental conditions, changing light flux in the environment may lead to enhanced Glc production/response and is a way to manipulate root architecture for optimized development via integrating several extrinsic and intrinsic signalling cues.