Arsenic, a non-nutrient metalloid is toxic to plants but many details on the physiology of plant adaptation to arsenic stress are not well understood. This work provides new insights about the role of sulfur assimilation in arsenate uptake, growth and arsenic tolerance. Research reported here indicates that two high affinity sulfate transporters in Arabidopsis thaliana are not involved in root uptake of arsenate. Further this study revealed that sulfate status influenced thiol levels, elemental nutrients, growth and arsenate tolerance. The hypothesis that arsenate may be transported via sulfate transporters, SULTR1;1 and SULTR1;2 in Arabidopsis, was tested. The double mutant of sultr1;1 sultr1;2 exhibited significantly less growth than the wild-type or the single mutants. The double mutant's sulfur content was significantly lower than the wild-type but the single mutants were similar to the wild-type confirming the redundant functions of SULTR1;1 and SULTR1;2. Gene expression analyses indicated that the double mutant's sulfate uptake could be explained by the expressions of SULTR1;3, SULTR2;1, and SULTR2;2 in its roots. Following arsenate supply to the roots, the double mutant accumulated significantly less arsenic in the roots and the shoots than did the single mutants and the wild-type. The double mutant accumulated significantly less potassium and phosphorus also. (35)S sulfate supplied to wild-type or double mutant roots showed that sulfate uptake was not inhibited by arsenate. Taken together, these results indicate that root uptake of arsenate is probably not via sulfate transporters, but the poor growth of the double mutant of sultr1;1 and sultr1;2 was due to its poor sulfate status and decreased levels of thiols, which had pleiotropic effects on the root uptake and translocation of potassium and phosphorus and arsenic tolerance.
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Alzheimers Dement
December 2024
Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Background: Calcineurin, a protein involved in functions such as synaptic plasticity and neuronal survival, plays an important role in the pathophysiology of Alzheimer's disease. This study, randomized, investigated the effects of FK506 (FK), a calcineurin inhibitor, on the behavioral, histological, and biochemical alterations observed in models of neurotoxicity induced by NMDA or Aβ and in a transgenic model for AD, in addition to the organotypic culture model stimulated with NMDA.
Methods: This study involved models for AD to experiment injecting NMDA or Aβ1-42 into the hippocampus of male C57Bl/6 mice aged 8-12 weeks to induce a neurotoxicity model, treating double-transgenic APP/PS1 mice, expressing both mouse/human APP and mutant human PS1, with chronic FK506 for AD, in which, to enable NMDA or Aβ1-42 microinjections, another experiment including a stereotaxic surgery was performed on the C57Bl/6 mice.
Nat Commun
January 2025
IBENS, Département de biologie, École normale supérieure, Université PSL, CNRS, INSERM, 75005, Paris, France.
Current temporal studies of DNA replication are either low-resolution or require complex cell synchronisation and/or sorting procedures. Here we introduce Nanotiming, a single-molecule, nanopore sequencing-based method producing high-resolution, telomere-to-telomere replication timing (RT) profiles of eukaryotic genomes by interrogating changes in intracellular dTTP concentration during S phase through competition with its analogue bromodeoxyuridine triphosphate (BrdUTP) for incorporation into replicating DNA. This solely demands the labelling of asynchronously growing cells with an innocuous dose of BrdU during one doubling time followed by BrdU quantification along nanopore reads.
View Article and Find Full Text PDFMethods Mol Biol
January 2025
Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Mosaic Analysis with Double Markers (MADM) represents a mouse genetic approach coupling differential fluorescent labeling to genetic manipulations in dividing cells and their lineages. MADM uniquely enables the generation and visualization of individual control or homozygous mutant cells in a heterozygous genetic environment. Among its diverse applications, MADM has been used to dissect cell-autonomous gene functions important for cortical development and neural development in general.
View Article and Find Full Text PDFJ Virol
December 2024
Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Protein kinase R (PKR) is an interferon-induced antiviral protein activated by autophosphorylation in response to double strand DNA (dsRNA) and other stimuli. Activated PKR causes translation inhibition and apoptosis, and it contributes to proinflammatory responses, cell growth, and differentiation. Mouse adenovirus type 1 (MAV-1) counteracts PKR by causing its degradation via a viral protein, early region 4 open reading frame 6 (E4orf6).
View Article and Find Full Text PDFmSphere
December 2024
Department of Microbiology, University of Georgia, Athens, Georgia, USA.
Unlabelled: Prominent virulence traits of include its ability to produce filamentous hyphal cells and grow as a biofilm. These traits are under control of numerous transcription factors (TFs), including Brg1 and Rme1. In the reference strain SC5314, a Δ/Δ mutant has reduced levels of biofilm/filament production; a Δ/Δ Δ/Δ double mutant has wild-type levels of biofilm/filament production.
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