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At least 19 recordsLinked to original sources
PubMed1996

How do plant shoots bend up? The initial step to elucidate the molecular mechanisms of shoot gravitropism using Arabidopsis thaliana.

In higher plants, shoots show a negative gravitropic response. To elucidate the molecular mechanisms of this phenomenon, mutational analyses using Arabidopsis thaliana are in progress. This minireview aims to present recent developments in the genetic analysis of shoot gravitropism in this organism. We focus mainly on our studies on the novel shoot gravitropic (sgr) mutants in Arabidopsis thaliana that have dramatic defects in shoot gravitropism.

Arabidopsis↗
PubMed2006

Physiological responses and tolerance of plant shoot to aluminum toxicity.

Aluminum (Al) toxicity is one of the most deleterious factors for plant growth in acidic soils because over 50% of the world's potentially arable lands are acidic. In recent years, considerable research has been conducted to understand the mechanisms of Al toxicity and tolerance in plants, and some review papers have been published. But most papers addressed mainly the mechanisms of Al toxicity and tolerance in plant root system, because inhibition of root growth is one of the earliest symptoms of Al injury and the most easily recognized symptom in solution culture. This paper reviews the effects of Al on photosynthesis, photoprotective systems, water use efficiency (WUE), water content, carbohydrate content, mineral nutrition, organic acids, and nitrogen metabolism in plant shoot, and also the mechanisms of Al detoxification (chelation of Al with small organic compounds, and isolating Al in the some parts, which are insensitive to Al, such as vacuoles or epidermal cells) by Al accumulators. Genetics and molecular biology of plant Al tolerance, as well as some aspects needed to be further studied are also discussed.

Adaptation, Physiological↗
PubMed2002

Tumorous shoot development (TSD) genes are required for co-ordinated plant shoot development.

This report describes the identification of novel plant genes that are required to ensure co-ordinated post-embryonic development. After germination the tumorous shoot development mutants of Arabidopsis thaliana develop disorganized tumorous tissue instead of organized leaves and stems. This results in green callus-like structures, which are capable of unlimited growth in vitro on hormone-free medium. The tsd mutants are recessive and belong to three complementation groups (tsd1, tsd2, tsd3). The genes were mapped to the bottom of chromosomes 5 and 1, and the top of chromosome 3, respectively. Histological analyses showed that the tsd mutants have different developmental defects. The shoot apical meristem of tsd1 formed only rudimentary leaves and was characterized by a degenerating L1 cell layer. tsd2 mutants had reduced cell adhesion and altered cell division planes in the L2 and L3 cell layers. The tumorous tissue of tsd3 mutants originated from the base of the leaf. Cytokinin levels that are inhibitory to the growth of wild-type seedlings bring about an enhanced growth response in all the tsd mutants. The steady state transcript levels of the histidine kinase CKI1 gene and the KNAT1 and STM homeobox genes were increased in tsd mutants, while mRNA levels of cell cycle genes were not altered. We hypothesize that the TSD gene products negatively regulate cytokinin-dependent meristematic activity during vegetative development of Arabidopsis.

Arabidopsis↗
PubMed2001

Functional domains in plant shoot meristems.

The development of higher plants depends on the activity of a shoot apical meristem. Organs are formed on the flanks of the meristem, while pluripotent stem cells are found in a separate domain in the meristem centre. Further domains are distinguished by the expression patterns of genes that control the development of the shoot meristem. Although most plant cells are immobile, their relative position within a meristem, and therefore also their function, can change after cell divisions. To maintain an active shoot meristem throughout plant life, the cells in the meristem need constantly to assess their position, transmit this information to others, and readjust their gene expression profiles and their fate. Some of the genes that permit intercellular communication have been isolated. They enable the flow of information in and between meristem regions via ligands and receptor proteins to transcription factors, that ultimately control the fate of cells in the centre of the meristem.

Animals↗
PubMed2006

Morphogenesis and patterning at the organ boundaries in the higher plant shoot apex.

Formation of lateral organ primordia from the shoot apical meristem creates boundaries that separate the primordium from surrounding tissue. Morphological and gene expression studies indicate the presence of a distinct set of cells that define the boundaries in the plant shoot apex. Cells at the boundary usually display reduced growth activity that results in separation of adjacent organs or tissues and this morphological boundary coincides with the border of different cell identities. Such morphogenetic and patterning events and their spatial coordination are controlled by a number of boundary-specific regulatory genes. The boundary may also act as a reference point for the generation of new meristems such as axillary meristems. Many of the genes involved in meristem initiation are expressed in the boundary. This review summarizes the cellular characters of the shoot organ boundary and the roles of regulatory genes that control different aspects of this unique region in plant development.

Arabidopsis↗
PubMed1986

Gravitropism in higher plant shoots. IV. Further studies on participation of ethylene.

Ethylene at 1.0 and 10.0 cubic centimeters per cubic meter decreased the rate of gravitropic bending in stems of cocklebur (Xanthium strumarium L.) and tomato (Lycopersicon esculentum Mill), but 0.1 cubic centimeter per cubic meter ethylene had little effect. Treating cocklebur plants with 1.0 millimolar aminoethoxyvinylglycine (AVG) (ethylene synthesis inhibitor) delayed stem bending compared with controls, but adding 0.1 cubic centimeter per cubic meter ethylene in the surrounding atmosphere (or applying 0.1% ethephon solution) partially restored the rate of bending of AVG-treated plants. Ethylene increases in bending stems, and AVG inhibits this. Virtually all newly synthesized ethylene appeared in bottom halves of horizontal stems, where ethylene concentrations were as much as 100 times those in upright stems or in top halves of horizontal stems. This was especially true when horizontal stems were physically restrained from bending. Ethylene might promote cell elongation in bottom tissues of a horizontal stem or indicate other factors there (e.g. a large amount of 'functioning' auxin). Or top and bottom tissues may become differentially sensitive to ethylene. Auxin applied to one side of a vertical stem caused extreme bending away from that side; gibberellic acid, kinetin, and abscisic acid were without effect. Acidic ethephon solutions applied to one side of young seedlings of cocklebur, tomato, sunflower (Helianthus annuus L.), and soybean (Glycine max [L.] Merr.) caused bending away from that side, but neutral ethephon solutions did not cause bending. Buffered or unbuffered acid (HCl) caused similar bending. Neutral ethephon solutions produced typical ethylene symptoms (i.e. epinasty, inhibition of stem elongation). HCl or acidic ethephon applied to the top of horizontal stems caused downward bending, but these substances applied to the bottom of such stems inhibited growth and upward bending--an unexpected result.

Dose-Response Relationship, Drug↗
PubMed2001

Function of plant shoot meristems.

Growth and development of higher plants is directed by the continuous activity of meristems, sites of sustained cell division. Organs are formed at the flanks of the shoot meristem, while the central region contains pluripotent stem cells. The developmental programme of the meristem is coordinated by interactions between cells in separate regions of meristems, and some of the genes involved have been studied. Transcription factors can be exchanged between meristem cell layers. The control of stem cell fate involves a ligand/receptor interaction that regulates the activity of a transcription factor, and genes expressed in organ primordia can feedback to restrict the activity of meristematic genes.

Cell Communication↗
PubMed2002

Age- and size-related trends in woody plant shoot development: regulatory pathways and evidence for genetic control.

Woody plants exhibit significant and predictable patterns of change in morphology and physiology as they become older and larger. Four models of potential pathways controlling these changes are presented: a stimulus-response model in which fully developed organs respond to changes in environment (defined here as everything external to the organ); an extrinsic model in which the attributes of developing organs are determined by environmental factors; an intrinsic model in which changes are a result of programmed changes in gene expression; and an extrinsic-intrinsic model in which changes in gene expression are induced by environmental factors. We review evidence that a genetic component is involved in controlling age- and size-related changes in foliar morphology and physiology and discuss the possibility of complex interactions among model pathways.

Models, Biological↗
PubMed2004

Nitrate assimilation in plant shoots depends on photorespiration.

Photorespiration, a process that diminishes net photosynthesis by approximately 25% in most plants, has been viewed as the unfavorable consequence of plants having evolved when the atmosphere contained much higher levels of carbon dioxide than it does today. Here we used two independent methods to show that exposure of Arabidopsis and wheat shoots to conditions that inhibited photorespiration also strongly inhibited nitrate assimilation. Thus, nitrate assimilation in both dicotyledonous and monocotyledonous species depends on photorespiration. This previously undescribed role for photorespiration (i) explains several responses of plants to rising carbon dioxide concentrations, including the inability of many plants to sustain rapid growth under elevated levels of carbon dioxide; and (ii) raises concerns about genetic manipulations to diminish photorespiration in crops.

Arabidopsis↗
PubMed1988

Gravitropism in higher plant shoots. V. Changing sensitivity to auxin.

An alternative to the Cholodny-Went, auxin-transport hypothesis of gravitropic stem bending was proposed as early as 1958, suggesting that gravistimulation induces changes in sensitivity to auxin, accounting for differential growth and bending. To test the sensitivity hypothesis, we immersed marked, decapitated sunflower (Helianthus annuus L.) hypocotyl sections in buffered auxin solutions over a wide concentration range (0, 10(-8) to 10(-2) molar IAA), photographed them at half-hour intervals, analyzed the negatives with a digitizer/computer, and evaluated surface-length changes in terms of Michaelis-Menten enzyme kinetics. Bending decreases with increasing auxin concentration; above about 10(-4) molar IAA the hypocotyls bend down; increasing auxin inhibits elongation growth of lower surfaces (which is high at zero or relatively low auxin levels) but promotes upper-surface growth (which is low at low auxin levels). Thus, lower surfaces have a greater Km sensitivity to applied auxin than upper surfaces. At optimum auxin levels (maximum growth), growth of bottom surfaces exceeds that of top surfaces, so bottom tissues have a greater Vmax sensitivity. Vmax sensitivity of vertical controls is slightly lower than it is for either horizontal surface; Km sensitivity is intermediate. Clearly, gravistimulation leads to significant changes in tissue sensitivity to applied auxin. Perhaps these changes are also important in normal gravitropism.

Dose-Response Relationship, Drug↗
PubMed2002

[Variability of life cycle traits in Iris pumila juvenile plants: plant shoots and roots dynamics].

In this study I analyzed dynamic of ramet number on 18 half-sib and 63 full-sib families of rhizomatous perennial herb Iris pumila originating from two Deliblato Sand populations and grown in two nutrient levels (full strength and 1/10 of full strength Hoagland solution). Contrary to most studies dealing with response to different nutrient availability, I failed to detect significant mean nutrient level effect on dynamic of module emergence. Such absence of consistent response to tenfold variation in solution strength indicate that I. pumila have low saturation rates of nutrient uptake and presumably experienced both utilized nutrition levels as rich ones. Genetic variability for plastic response was lacking either. On the other hand, presence of between-population differentiation for the trait itself indicates that I. pumila harbors considerable amounts of within-species genetic variability for ramet dynamics.

Crosses, Genetic↗
PubMed2006

Maize response to acute arsenic toxicity as revealed by proteome analysis of plant shoots.

Aerial parts (shoots) of maize seedlings fed hydroponically with 300 muM sodium arsenate [As(V)] or 250 muM sodium arsenite [As(III)] for 24 h were analyzed for differentially expressed proteins by 2-DE and digital image analysis. About 15% of total detected proteins (74 out of 500) were up- or, mainly, down-regulated by arsenic, among which 14 were selected as being those most affected by the metalloid. These proteins were analyzed by MALDI-TOF MS and 7 of them were identified: translation initiation factor eIF-5A, ATP synthase, cysteine synthase, malate dehydrogenase, protein kinase C inhibitor, Tn10 transposase-like protein, and guanine nucleotide binding protein. Each of these proteins was completely repressed by As(V) and/or As(III), except protein kinase C inhibitor, which was newly detected after exposure to As(V).

Arsenic↗
PubMed1984

A transmissible plant shoot factor promotes uptake hydrogenase activity in Rhizobium symbionts.

Shoot/root grafting studies showed organ and host cultivar effects on net H(2) evolution from Pisum sativum L. root nodules. Net H(2) evolution from those nodules represents the sum of H(2) formed by Rhizobium nitrogenase and H(2) oxidized by any uptake hydrogenase present in the bacteria. Grafts between pea cultivars ;JI1205' or ;Alaska' and ;Feltham First' in symbioses with R. leguminosarum 128C53 showed that shoots of both JI1205 and Alaska increased H(2) uptake significantly (P </= 0.05) in Feltham First root nodules. The same plants also had less net H(2) evolution at similar rates of C(2)H(2) reduction than plants formed by grafting Feltham First shoots on Feltham First roots. Although JI1205 and Alaska shoots increased H(2)-uptake activity of Feltham First root nodules 28 days after the graft was made, intermediate to high levels of H(2) uptake activity were still present in nodules on roots of both JI1205 and Alaska grafted to Feltham First shoots. These results indicate the presence of a transmissible shoot factor(s) which can increase uptake hydrogenase activity in a Rhizobium symbiont and show that root genotype also can influence that parameter.Parallel grafting experiments using the same pea cultivars in symbioses with R. leguminosarum strain 300, which lacks uptake hydrogenase activity, suggested that a transmissible shoot factor(s) altered H(2) formation from nitrogenase by changing the electron allocation coefficient of that enzyme complex.The root and shoot factor(s) detected in this study had no permanent effect on strain 128C53. Bacterial cells isolated from Feltham First nodules with low H(2) uptake activity formed root nodules on JI1205 and Alaska with high H(2) uptake activity. Bacteroids isolated from nodules on intact JI1205, Alaska, or Feltham First plants with high, medium, or low H(2) uptake activity, respectively, maintained those phenotypes during in vitro assays.

Journal Article↗