The Arabidopsis selenium-binding protein confers tolerance to toxic levels of selenium

2005 ◽  
Vol 32 (10) ◽  
pp. 881 ◽  
Author(s):  
Adamantia Agalou ◽  
Andreas Roussis ◽  
Herman P. Spaink
Keyword(s):  
Transgenic Plants ◽  
Gene Silencing ◽  
Binding Protein ◽  
Normal Growth ◽  
Growth Conditions ◽  
Growth Responses ◽  
Wild Type ◽  
Selenium Toxicity ◽  
Transcript Levels ◽  
Expression Levels

In the Arabidopsis genome there are three highly conserved homologues of the mammalian 56-kD selenium-binding protein (SBP). To study the function of SBP in this model plant, we used a transgenic approach by constitutively overexpressing and down-regulating the endogenous Atsbp1 gene. In the latter case, we employed both a conventional antisense method and gene silencing by intron-containing hairpin RNAs. Atsbp1-overexpressing and silenced plants were phenotypically normal, under standard growth conditions, when compared with wild type plants. Transgenic plants exhibited different growth responses to exogenously supplied selenite, which correlated with the expression levels of Atsbp1. Plants with increased Atsbp1 transcript levels showed enhanced tolerance to selenite, while plants with reduced levels were more sensitive. Our results indicate that, although Atsbp1 does not play a detectable role in the regulation of developmental processes under normal growth conditions, it appears to be involved in processes controlling tolerance of Arabidopsis to selenium toxicity.

scholarly journals MtBZR1 Plays an Important Role in Nodule Development in Medicago truncatula

2019 ◽  
Vol 20 (12) ◽  
pp. 2941
Author(s):  
Can Cui ◽  
Hongfeng Wang ◽  
Limei Hong ◽  
Yiteng Xu ◽  
Yang Zhao ◽  
...  
Keyword(s):  
Medicago Truncatula ◽  
Sinorhizobium Meliloti ◽  
Normal Growth ◽  
Dry Mass ◽  
Growth Conditions ◽  
Nodule Development ◽  
Functional Study ◽  
Loss Of Function ◽  
Wild Type

Brassinosteroid (BR) is an essential hormone in plant growth and development. The BR signaling pathway was extensively studied, in which BRASSINAZOLE RESISTANT 1 (BZR1) functions as a key regulator. Here, we carried out a functional study of the homolog of BZR1 in Medicago truncatula R108, whose expression was induced in nodules upon Sinorhizobium meliloti 1021 inoculation. We identified a loss-of-function mutant mtbzr1-1 and generated 35S:MtBZR1 transgenic lines for further analysis at the genetic level. Both the mutant and the overexpression lines of MtBZR1 showed no obvious phenotypic changes under normal growth conditions. After S. meliloti 1021 inoculation, however, the shoot and root dry mass was reduced in mtbzr1-1 compared with the wild type, caused by partially impaired nodule development. The transcriptomic analysis identified 1319 differentially expressed genes in mtbzr1-1 compared with wild type, many of which are involved in nodule development and secondary metabolite biosynthesis. Our results demonstrate the role of MtBZR1 in nodule development in M. truncatula, shedding light on the potential role of BR in legume–rhizobium symbiosis.

scholarly journals Use of Inducible Feedback-ResistantN-Acetylglutamate Synthetase (argA) Genes for Enhanced Arginine Biosynthesis by Genetically EngineeredEscherichia coli K-12 Strains

1998 ◽  
Vol 64 (5) ◽  
pp. 1805-1811 ◽  
Author(s):  
B. S. Rajagopal ◽  
Joseph DePonte ◽  
Mendel Tuchman ◽  
Michael H. Malamy
Keyword(s):  
Feedback Inhibition ◽  
Expression System ◽  
Point Mutations ◽  
Normal Growth ◽  
Growth Conditions ◽  
Wild Type ◽  
Arginine Biosynthesis ◽  
E Coli ◽  
Genes Encoding ◽  
K 12

ABSTRACT The goal of this work was to construct Escherichia colistrains capable of enhanced arginine production. The arginine biosynthetic capacity of previously engineered E. colistrains with a derepressed arginine regulon was limited by the availability of endogenous ornithine (M. Tuchman, B. S. Rajagopal, M. T. McCann, and M. H. Malamy, Appl. Environ. Microbiol. 63:33–38, 1997). Ornithine biosynthesis is limited due to feedback inhibition by arginine of N-acetylglutamate synthetase (NAGS), the product of the argA gene and the first enzyme in the pathway of arginine biosynthesis in E. coli. To circumvent this inhibition, the argA genes from E. coli mutants with feedback-resistant (fbr) NAGS were cloned into plasmids that contain “arg boxes,” which titrate the ArgR repressor protein, with or without the E. coli carABgenes encoding carbamyl phosphate synthetase and the argIgene for ornithine transcarbamylase. The free arginine production rates of “arg-derepressed” E. coli cells overexpressing plasmid-encoded carAB, argI, and fbr argA genes were 3- to 15-fold higher than that of an equivalent system overexpressing feedback-sensitive wild-type (wt)argA. The expression system with fbr argAproduced 7- to 35-fold more arginine than a system overexpressingcarAB and argI genes on a plasmid in a strain with a wt argA gene on the chromosome. The arginine biosynthetic capacity of arg-derepressed DH5α strains with plasmids containing only the fbr argA gene was similar to that of cells with plasmids also containing the carABand argI genes. Plasmids containing wt or fbrargA were stably maintained under normal growth conditions for at least 18 generations. DNA sequencing identified different point mutations in each of the fbr argA mutants, specifically H15Y, Y19C, S54N, R58H, G287S, and Q432R.

Growth Responses in Sorghum and Wheat Induced by Glyphosate

Weed Science ◽  
1977 ◽  
Vol 25 (3) ◽  
pp. 238-240 ◽  
Author(s):  
J.R. Baur ◽  
R.W. Bovey ◽  
J.A. Veech
Keyword(s):  
Foliar Application ◽  
Normal Growth ◽  
Growth Zone ◽  
Growth Conditions ◽  
Optimum Growth ◽  
Growth Responses ◽  
Fresh Weight ◽  
Optimum Growth Temperature ◽  
Chamber Studies ◽  
Growth Chamber Studies

Foliar application of 2.8 μg/plant of glyphosate [N-(phosphonomethyl)glycine] to greenhouse grown sorghum [Sorghum bicolor (L.) Moench ‘Tophand’] seedlings resulted in increased fresh weight. As glyphosate levels were increased to 11.2 μg/plant, diameter of the basal growth zone increased while fresh weight decreased. In growth chamber studies with sorghum and wheat [Triticum aestivum (L.) ‘Era’] seedlings, glyphosate caused the greatest reduction in fresh weight at the optimum growth temperatures for both species. Glyphosate inhibited normal production of basal buds in wheat at the optimum growth temperature and stimulated bud production at temperatures above the optimum. Under normal growth conditions, basal buds in sorghum do not develop; however, application of glyphosate stimulated basal bud development under normal and above-normal temperature conditions. Histochemical analysis of malate dehydrogenase activity in apical meristem tissue of treated sorghum seedlings indicated that growth of the apex was normal and viable.

scholarly journals The Nuclear Pore Complex and the DEAD Box Protein Rat8p/Dbp5p Have Nonessential Features Which Appear To Facilitate mRNA Export following Heat Shock

2004 ◽  
Vol 24 (11) ◽  
pp. 4869-4879 ◽  
Author(s):  
Christiane Rollenhagen ◽  
Christine A. Hodge ◽  
Charles N. Cole
Keyword(s):  
Heat Shock ◽  
Mrna Export ◽  
Normal Growth ◽  
Growth Conditions ◽  
Nuclear Pore ◽  
Nuclear Pore Complexes ◽  
Wild Type ◽  
Dead Box ◽  
Rna Export ◽  
Pore Complexes

ABSTRACT Nuclear pore complexes (NPCs) play an essential role in RNA export. Nucleoporins required for mRNA export in Saccharomyces cerevisiae are found in the Nup84p and Nup82p subcomplexes of the NPC. The Nup82p subcomplex contains Nup82p, Rat7p/Nup159p, Nsp1p, Gle1p/Rss1p, and Rip1p/Nup42p and is found only on the cytoplasmic face of NPCs. Both Rat7p and Gle1p contain binding sites for Rat8p/Dbp5p, an essential DEAD box protein and putative RNA helicase. Rip1p interacts directly with Gle1p and is the only protein known to be essential for mRNA export after heat shock but not under normal growth conditions. We report that in cells lacking Rip1p, both Gle1p and Rat8p dissociate from NPCs following heat shock at 42°C. Rat8p but not Gle1p was retained at NPCs if rip1Δ cells were first shifted to 37°C and then to 42°C, and this was correlated with preserving mRNA export in heat-shocked rip1Δ cells. Export following ethanol shock was less dependent on the presence of Rip1p. Exposure to 10% ethanol led to dissociation of Rat8p from NPCs in both wild-type and rip1Δ cells. Following this treatment, Rat8p was primarily nuclear in wild-type cells but primarily cytoplasmic in rip1Δ cells. We also determined that efficient export of heat shock mRNA after heat shock depends upon a novel 6-amino-acid element within Rat8p. This motif is not required under normal growth conditions or following ethanol shock. These studies suggest that the molecular mechanism responsible for the defect in export of heat shock mRNAs in heat-shocked rip1Δ cells is dissociation of Rat8p from NPCs. These studies also suggest that both nuclear pores and Rat8p have features not required for mRNA export in growing cells but which enhance the ability of mRNAs to be exported following heat shock.

scholarly journals Isolation and Functional Characterization of a Salt-Responsive Calmodulin-Like Gene MpCML40 from Semi-Mangrove Millettia pinnata

2021 ◽  
Vol 22 (7) ◽  
pp. 3475
Author(s):  
Yi Zhang ◽  
Jianzi Huang ◽  
Qiongzhao Hou ◽  
Yujuan Liu ◽  
Jun Wang ◽  
...  
Keyword(s):  
Salt Stress ◽  
Salt Tolerance ◽  
Transgenic Plants ◽  
Heterologous Expression ◽  
Germination Rate ◽  
Functional Characterization ◽  
Normal Growth ◽  
Growth Conditions ◽  
Yeast Cells ◽  
Millettia Pinnata

Salt stress is a major increasing threat to global agriculture. Pongamia (Millettia pinnata), a semi-mangrove, is a good model to study the molecular mechanism of plant adaptation to the saline environment. Calcium signaling pathways play critical roles in the model plants such as Arabidopsis in responding to salt stress, but little is known about their function in Pongamia. Here, we have isolated and characterized a salt-responsive MpCML40, a calmodulin-like (CML) gene from Pongamia. MpCML40 protein has 140 amino acids and is homologous with Arabidopsis AtCML40. MpCML40 contains four EF-hand motifs and a bipartite NLS (Nuclear Localization Signal) and localizes both at the plasma membrane and in the nucleus. MpCML40 was highly induced after salt treatment, especially in Pongamia roots. Heterologous expression of MpCML40 in yeast cells improved their salt tolerance. The 35S::MpCML40 transgenic Arabidopsis highly enhanced seed germination rate and root length under salt and osmotic stresses. The transgenic plants had a higher level of proline and a lower level of MDA (malondialdehyde) under normal and stress conditions, which suggested that heterologous expression of MpCML40 contributed to proline accumulation to improve salt tolerance and protect plants from the ROS (reactive oxygen species) destructive effects. Furthermore, we did not observe any measurable discrepancies in the development and growth between the transgenic plants and wild-type plants under normal growth conditions. Our results suggest that MpCML40 is an important positive regulator in response to salt stress and of potential application in producing salt-tolerant crops.

scholarly journals Threshold and adaptation in Phycomyces. Their interrelation and regulation by light.

1984 ◽  
Vol 84 (1) ◽  
pp. 119-132 ◽  
Author(s):  
P Galland ◽  
V E Russo
Keyword(s):  
Growth Rate ◽  
Dark Adaptation ◽  
Type Strain ◽  
Wild Type Strain ◽  
Light Sensitivity ◽  
Growth Conditions ◽  
Continuous Illumination ◽  
Growth Responses ◽  
Wild Type

The absolute light sensitivity of Phycomyces sporangiophores was determined by analyzing the intensity dependence of the phototropic bending rate and of the light growth and dark growth responses to step changes of the intensity. We found that the different methods give approximately the same results for the wild-type strain, as well as for several behavioral mutants with defects in the genes madA, madB, and madC. A crucial factor in the determination of thresholds is the light intensity at which the strains grow during the 4 d after inoculation and prior to the experiment. When the wild-type strain grows in the dark, its threshold for the bending rate is 10(-9) W X m-2, compared with 2 X 10(-7) W X m-2 when it is grown under continuous illumination. Further, the maximal bending rate is twice as high in dark-grown strains. This phenomenon is further complicated by the fact that the diameter and growth rate of the sporangiophores also depend on the illumination conditions prior to the experiment: light-grown sporangiophores have an increased diameter and an increased growth rate compared with dark-grown ones. Some of the behavioral mutants, however, are indifferent to this form of light control. Another factor that is controlled by the growth conditions is adaptation: the kinetics of dark adaptation are slower in light-grown sporangiophores than in dark-grown ones. We found empirically a positive correlation between the slower dark adaptation constant and the threshold of the bending rate, which shows that the two underlying phenomena are functionally related.

scholarly journals The Arabidopsis thaliana E3 Ubiquitin Ligase BRIZ Functions in Abscisic Acid Response

2021 ◽  
Vol 12 ◽  
Author(s):  
Katrina J. Linden ◽  
Mon Mandy Hsia ◽  
Yi-Tze Chen ◽  
Judy Callis
Keyword(s):  
Arabidopsis Thaliana ◽  
Abscisic Acid ◽  
E3 Ligase ◽  
Normal Growth ◽  
Growth Conditions ◽  
Aba Signaling ◽  
Wild Type ◽  
Ubiquitin System ◽  
Early Seedling ◽  
Cotyledon Expansion

The ubiquitin system is essential for multiple hormone signaling pathways in plants. Here, we show that the Arabidopsis thaliana E3 ligase BRIZ, a heteromeric ligase that consists minimally of BRIZ1 and BRIZ2 proteins, functions in abscisic acid (ABA) signaling or response. briz1 and briz2 homozygous mutants either fail to germinate or emerge later than wild-type seedlings, with little cotyledon expansion or root elongation and no visible greening. Viability staining indicates that briz1 and briz2 embryos are alive but growth-arrested. Germination of briz mutants is improved by addition of the carotenoid biosynthetic inhibitor fluridone or gibberellic acid (GA3), and briz mutants have improved development in backgrounds deficient in ABA synthesis (gin1-3/aba2) or signaling (abi5-7). Endogenous ABA is not higher in briz2 seeds compared to wild-type seeds, and exogenous ABA does not affect BRIZ mRNAs in imbibed seeds. These results indicate that briz embryos are hypersensitive to ABA and that under normal growth conditions, BRIZ acts to suppress ABA signaling or response. ABA signaling and sugar signaling are linked, and we found that briz1 and briz2 mutants excised from seed coats are hypersensitive to sucrose. Although briz single mutants do not grow to maturity, we were able to generate mature briz2-3 abi5-7 double mutant plants that produced seeds. These seeds are more sensitive to exogenous sugar and are larger than seeds from sibling abi5-7 BRIZ2/briz2-3 plants, suggesting that BRIZ has a parental effect on seed development. From these data, we propose a model in which the BRIZ E3 ligase suppresses ABA responses during seed maturation and germination and early seedling establishment.

Comparison ofbax,waf1, and IMP dehydrogenase regulation in response to wild-type p53 expression under normal growth conditions

1998 ◽  
Vol 177 (2) ◽  
pp. 364-376 ◽  
Author(s):  
Yuan Liu ◽  
Lee B. Riley ◽  
Shirley A. Bohn ◽  
Judith A. Boice ◽  
Patrizia B. Stadler ◽  
...  
Keyword(s):  
Normal Growth ◽  
Growth Conditions ◽  
Wild Type ◽  
P53 Expression ◽  
Imp Dehydrogenase ◽  
Wild Type P53

scholarly journals Antioxidant Functions of Nitric Oxide Synthase in a Methicillin SensitiveStaphylococcus aureus

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Manisha Vaish ◽  
Vineet K. Singh
Keyword(s):  
Oxidative Stress ◽  
Nitric Oxide ◽  
Nitric Oxide Synthase ◽  
Normal Growth ◽  
Growth Conditions ◽  
Nitric Oxide Donor ◽  
Wild Type ◽  
Gene Encoding ◽  
Stress Studies ◽  
Oxide Synthase

Nitric oxide and its derivative peroxynitrites are generated by host defense system to control bacterial infection. However certain Gram positive bacteria includingStaphylococcus aureuspossess a gene encoding nitric oxide synthase (SaNOS) in their chromosome. In this study it was determined that under normal growth conditions, expression ofSaNOSwas highest during early exponential phase of the bacterial growth. In oxidative stress studies, deletion ofSaNOSled to increased susceptibility of the mutant cells compared to wild-typeS. aureus. While inhibition ofSaNOSactivity by the addition of L-NAME increased sensitivity of the wild-typeS. aureusto oxidative stress, the addition of a nitric oxide donor, sodium nitroprusside, restored oxidative stress tolerance of theSaNOSmutant. TheSaNOSmutant also showed reduced survival after phagocytosis by PMN cells with respect to wild-typeS. aureus.

Although calnexin is essential in S. pombe, its highly conserved central domain is dispensable for viability

1999 ◽  
Vol 112 (23) ◽  
pp. 4449-4460 ◽  
Author(s):  
A. Elagoz ◽  
M. Callejo ◽  
J. Armstrong ◽  
L.A. Rokeach
Keyword(s):  
Central Region ◽  
Mammalian Cells ◽  
Normal Growth ◽  
Optimal Growth ◽  
Growth Conditions ◽  
Wild Type ◽  
Lectin Activity ◽  
Central Domain ◽  
Folding Intermediates ◽  
Mutant Cells

In mammalian cells, the calnexin/calreticulin chaperones play a key role in glycoprotein folding and its control within the endoplasmic reticulum (ER), by interacting with folding intermediates via their monoglucosylated glycans. This lectin activity has been mapped in mammalian calnexin/calreticulin chaperones to the central region, which is a highly conserved feature of calnexin/calreticulin molecules across species. The central domain has also been implicated in Ca(2+) binding, and it has been proposed to be involved in the regulation of calcium homeostasis in the ER. Herein, we show that although the Schizosaccharomyces pombe calnexin is essential for viability, cells lacking its 317-amino-acid highly conserved central region are viable under normal growth conditions. However, the central region appears to be necessary for optimal growth under high ER-stress, suggesting that this region is important under extreme folding situations (such as DTT and temperature). The minimal length of calnexin required for viability spans the C-terminal 123 residues. Furthermore, cells with the central domain of the protein deleted were affected in their morphology at 37 degrees C, probably due to a defect in cell wall synthesis, although these mutant cells exhibited the same calcium tolerance as wild-type cells at 30 degrees C.

Sign in / Sign up

Export Citation Format

Share Document