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Among different environmental stresses,cold stress can significantly affect plant's physiological activity, biochemical metabolism, growth, development and crop productivity. Problems due to cold stress should be addressed seriously keeping in concern extreme temperature events due to climate change, alarming increase in population growth and demanding food needs. Cold signal is recognized by receptors of cell membrane, severity of which is determined by factors like light and temperature. The signal is transduced by cold responsive genes, second messengers like calcium and transcription factors to exert symptoms including decreased germination, stunted growth, chlorosis, wilting of leaves, compromised reproductive development and ultimately necrosis. Cold stress induces cell membrane damage, reduction in scavenging enzymes' activity, loss of energy in photosynthetic apparatus and stability of proteins. This review presents a broader overview of components regulating cold stress responses, changes in physiological processes, transcriptional; post-transcriptional regulations,coldsignaling pathway and interactions with photoreceptors, phytohormones, pathogenesis-related genes, microbial interactions during cold stress. Keywords Cold tolerance--Cold binding Factor, Phytochrome * Cold acclimation * Freezing tolerance * Phytohormones * Circadian clock genes, Introduction Plants are forced to adapt to the prevailing environment surrounding them since they are unable to migrate under unfavourable climatic conditions. About 64% of the entire earth acreage hasaverageminimum [...]

Key message: Inclusion of carbon nanoparticles in growth medium accelerates timing to flower by down-regulating phytochrome B in a CONSTANS-independent but photoperiod-dependent manner in Arabidopsis thaliana.Abstract: Despite the recognized importance of nanoparticles in plant development over the last decade, the effect of carbon nanoparticles (CNPs) on plant processes such as photomorphogenesis and flowering time control is poorly understood. We explored the uptake, accumulation and effect of CNPs on seedling development and flowering time control in Arabidopsis thaliana (At). CNPs uptake was demonstrated using Raman spectroscopy and light microscopy that affected At seedling growth and flowering time in a dose-dependent manner. The highest accumulation of CNPs was observed in leaves followed by stem and root tissues. CNPs treatment enhanced seed germination, showed elongated hypocotyl, larger cotyledon area and increased chlorophyll content in At seedlings. CNPs treatment induced early flowering in both long-day and short-day growth conditions indicating a photoperiod-dependent effect. CNPs-treated seedlings showed a drastic reduction in the relative abundance of phytochrome B (PHYB) transcript. Further, we analyzed the transcript abundance of at least one major component involved in various pathways that regulate flowering such as (1) photoperiod, (2) gibberellic acid (GA), (3) vernalization and (4) autonomous. An up-regulation of transcript levels of PHYTOCHROME INTERACTING FACTOR 4 (PIF4), GIGANTEA (GI), REPRESSOR OF GIBBERELLIC ACID 1 (RGA1) and LEAFY (LFY) were observed, however, there were no changes in the transcript levels of CONSTANS (CO), VERNALIZATION 1 (VRN1) and FLOWERING CONTROL LOCUS A (FCA). Despite the up-regulation of RGA1, we conclude that the earlier flowering is most likely GA-independent. Here, we demonstrated that the early flowering in CNPs-treated seedlings was PHYB and photoperiod-dependent. [ABSTRACT FROM AUTHOR]

Development of phosphate (P)-deficiency tolerant rice cultivars is constrained by lack of suitable, reproducible, and consistent seedling stage screening methods in breeding programs. This study reports the screening and characterization of M5 mutants derived from an ethyl methane sulfonate treated population of ricecv.Nagina 22 (N22) in low-P field (soil Olsen P 1.94–2.01 mg kg−1; alkaline Vertisol; pH 7.94) for high yield. The present study showed that seedling growth responses such as increase in root weight, root length, root/shoot weight, and dry weight in P-deficient medium can be taken as indices of low-P tolerance in mature plants in field. Total phosphorus content in seedlings showed an inverse relationship with total phosphorus content and low-P tolerance in mature plants in the field. But, phosphorus content in seeds and acid phosphatase activity in the seedling stage were positively correlated with survival and seed set in low-P field. In low-P field, plant height correlated most with yield per plant, and the number of productive tillers in mature plants was highly correlated with tiller number at vegetative stage. These mutants (NH776, NH710,andNH719) have agronomic importance because of their ability to grow and give higher yield than N22 in P-deficient field. [ABSTRACT FROM AUTHOR]

GIGANTEA is a multifaceted plant-specific protein that originated in a streptophyte ancestor. The current known functions of GI include circadian clock control, light signalling, flowering time regulation, stomata response, chloroplast biogenesis, accumulation of anthocyanin, chlorophyll, and starch, phytohormone signalling, senescence and response to drought, salt, and oxidative stress. Six decades since its discovery, no functional domains have been defined, and its mechanism of action is still not well-characterised. In this review, we explore the functional evolution of GI to distinguish between ancestral and more recently acquired roles. GI integrated itself into various existing signalling pathways of the circadian clock, blue light, photoperiod, and osmotic and oxidative stress response. It also evolved parallelly to acquire new functions for chloroplast accumulation, red light signalling and anthocyanin production. In this review, we have encapsulated the known mechanisms of various biological functions of GI. Additionally, this manuscript will throw light on the evolution of GI in plant lineage., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)