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1.
J Integr Plant Biol ; 63(8): 1537-1554, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34009694

ABSTRACT

Plants have a hierarchical circadian structure comprising multiple tissue-specific oscillators that operate at different speeds and regulate the expression of distinct sets of genes in different organs. However, the identity of the genes differentially regulated by the circadian clock in different organs, such as roots, and how their oscillations create functional specialization remain unclear. Here, we profiled the diurnal and circadian landscapes of the shoots and roots of Medicago truncatula and identified the conserved regulatory sequences contributing to transcriptome oscillations in each organ. We found that the light-dark cycles strongly affect the global transcriptome oscillation in roots, and many clock genes oscillate only in shoots. Moreover, many key genes involved in nitrogen fixation are regulated by circadian rhythms. Surprisingly, the root clock runs faster than the shoot clock, which is contrary to the hierarchical circadian structure showing a slow-paced root clock in both detached and intact Arabidopsis thaliana (L.) Heynh. roots. Our result provides important clues about the species-specific circadian regulatory mechanism, which is often overlooked, and possibly coordinates the timing between shoots and roots independent of the current prevailing model.


Subject(s)
Circadian Clocks/physiology , Circadian Rhythm/physiology , Medicago truncatula/physiology , Plant Roots/physiology , Circadian Clocks/genetics , Circadian Clocks/radiation effects , Circadian Rhythm/genetics , Circadian Rhythm/radiation effects , Gene Expression Regulation, Plant/radiation effects , Genes, Plant , Light , Medicago truncatula/genetics , Medicago truncatula/radiation effects , Nitrogen Fixation/genetics , Nitrogen Fixation/radiation effects , Organ Specificity/genetics , Organ Specificity/radiation effects , Plant Roots/genetics , Plant Roots/radiation effects , Plant Shoots/genetics , Plant Shoots/physiology , Plant Shoots/radiation effects , Promoter Regions, Genetic/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Species Specificity , Transcription, Genetic/radiation effects , Transcriptome/genetics
2.
Int J Mol Sci ; 21(22)2020 Nov 19.
Article in English | MEDLINE | ID: mdl-33228084

ABSTRACT

Polar auxin transport mediated by PIN-FORMED (PIN) proteins is critical for plant growth and development. As an environmental cue, shade stimulates hypocotyls, petiole, and stem elongation by inducing auxin synthesis and asymmetric distributions, which is modulated by PIN3,4,7 in Arabidopsis. Here, we characterize the MtPIN1 and MtPIN3, which are the orthologs of PIN3,4,7, in model legume species Medicago truncatula. Under the low Red:Far-Red (R:FR) ratio light, the expression of MtPIN1 and MtPIN3 is induced, and shadeavoidance response is disrupted in mtpin1 mtpin3 double mutant, indicating that MtPIN1 and MtPIN3 have a conserved function in shade response. Surprisingly, under the normal growth condition, mtpin1 mtpin3 displayed the constitutive shade avoidance responses, such as the elongated petiole, smaller leaf, and increased auxin and chlorophyll content. Therefore, MtPIN1 and MtPIN3 play dual roles in regulation of shadeavoidance response under different environments. Furthermore, these data suggest that PIN3,4,7 and its orthologs have evolved conserved and specific functions among species.


Subject(s)
Arabidopsis Proteins/genetics , Gene Expression Regulation, Plant , Medicago truncatula/genetics , Membrane Transport Proteins/genetics , Plant Leaves/genetics , Arabidopsis/genetics , Arabidopsis/growth & development , Arabidopsis/metabolism , Arabidopsis/radiation effects , Arabidopsis Proteins/metabolism , Chlorophyll/biosynthesis , Chlorophyll/genetics , Conserved Sequence , Gene Expression Regulation, Developmental , Hypocotyl/genetics , Hypocotyl/growth & development , Hypocotyl/metabolism , Hypocotyl/radiation effects , Indoleacetic Acids/metabolism , Indoleacetic Acids/pharmacology , Light , Medicago truncatula/growth & development , Medicago truncatula/metabolism , Medicago truncatula/radiation effects , Membrane Transport Proteins/metabolism , Mutation , Photosynthesis/genetics , Plant Growth Regulators/metabolism , Plant Growth Regulators/pharmacology , Plant Leaves/growth & development , Plant Leaves/metabolism , Plant Leaves/radiation effects , Protein Isoforms/genetics , Protein Isoforms/metabolism
3.
J Vis Exp ; (129)2017 11 08.
Article in English | MEDLINE | ID: mdl-29155794

ABSTRACT

Mutants are invaluable genetic resources for gene function studies. To generate mutant collections, three types of mutagens can be utilized, including biological such as T-DNA or transposon, chemical such as ethyl methanesulfonate (EMS), or physical such as ionization radiation. The type of mutation observed varies depending on the mutagen used. For ionization radiation induced mutants, mutations include deletion, duplication, or rearrangement. While T-DNA or transposon-based mutagenesis is limited to species that are susceptible to transformation, chemical or physical mutagenesis can be applied to a broad range of species. However, the characterization of mutations derived from chemical or physical mutagenesis traditionally relies on a map-based cloning approach, which is labor intensive and time consuming. Here, we show that a high-density genome array-based comparative genomic hybridization (aCGH) platform can be applied to efficiently detect and characterize copy number variations (CNVs) in mutants derived from fast neutron bombardment (FNB) mutagenesis in Medicago truncatula, a legume species. Whole genome sequence analysis shows that there are more than 50,000 genes or gene models in M. truncatula. At present, FNB-induced mutants in M. truncatula are derived from more than 150,000 M1 lines, representing invaluable genetic resources for functional studies of genes in the genome. The aCGH platform described here is an efficient tool for characterizing FNB-induced mutants in M. truncatula.


Subject(s)
Comparative Genomic Hybridization/methods , DNA Copy Number Variations , Fast Neutrons , Medicago truncatula/genetics , Medicago truncatula/radiation effects , Mutation
4.
J Environ Radioact ; 141: 57-61, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25540940

ABSTRACT

Contamination of soils with radioisotopes of caesium (Cs) is of concern because of their emissions of harmful ß and γ radiation. Radiocaesium enters the food chain through vegetation and the intake of Cs can affect the health of organisms. Arbuscular mycorrhizal (AM) fungi form mutualistic symbioses with plants through colonization of the roots and previous studies on the influence of AM on Cs concentrations in plants have given inconsistent results. These studies did not investigate the influence of Cs on AM fungi and it is therefore not known if Cs has a direct effect on AM colonization. Here, we investigated whether Cs influences AM colonization and if this effect impacts on the influence of Rhizophagus intraradices on Cs accumulation by Medicago truncatula. M. truncatula was grown with or without R. intraradices in pots containing different concentrations of Cs. Here, we present the first evidence that colonization of plants by AM fungi can be negatively affected by increasing Cs concentrations in the soil. Mycorrhizal colonization had little effect on root or shoot Cs concentrations. In conclusion, the colonization by AM fungi is impaired by high Cs concentrations and this direct effect of soil Cs on AM colonization might explain the inconsistent results reported in literature that have shown increased, decreased or unaffected Cs concentrations in AM plants.


Subject(s)
Cesium Radioisotopes/toxicity , Glomeromycota/radiation effects , Medicago truncatula/metabolism , Mycorrhizae/radiation effects , Soil Pollutants, Radioactive/toxicity , Glomeromycota/growth & development , Glomeromycota/physiology , Medicago truncatula/microbiology , Medicago truncatula/radiation effects , Mycorrhizae/growth & development
5.
PLoS One ; 7(7): e41567, 2012.
Article in English | MEDLINE | ID: mdl-22859998

ABSTRACT

Third party species, which interact with one or both partners of a pairwise species interaction, can shift the ecological costs and the evolutionary trajectory of the focal interaction. Shared genes that mediate a host's interactions with multiple partners have the potential to generate evolutionary constraints, making multi-player interactions critical to our understanding of the evolution of key interaction traits. Using a field quantitative genetics approach, we studied phenotypic and genetic correlations among legume traits for rhizobium and herbivore interactions in two light environments. Shifts in plant biomass allocation mediated negative phenotypic correlations between symbiotic nodule number and herbivory in the field, whereas positive genetic covariances suggested shared genetic pathways between nodulation and herbivory response. Trait variance-covariance (G) matrices were not equal in sun and shade, but nevertheless responses to independent and correlated selection are expected to be similar in both environments. Interactions between plants and aboveground antagonists might alter the evolutionary potential of traits mediating belowground mutualisms (and vice versa). Thus our understanding of legume-rhizobium genetics and coevolution may be incomplete without a grasp of how these networks overlap with other plant interactions.


Subject(s)
Evolution, Molecular , Medicago truncatula/genetics , Rhizobium/genetics , Animals , Biomass , Genetic Variation , Herbivory , Medicago truncatula/growth & development , Medicago truncatula/microbiology , Medicago truncatula/radiation effects , Models, Genetic , Multivariate Analysis , Phenotype , Plant Shoots/genetics , Plant Shoots/growth & development , Plant Shoots/microbiology , Plant Shoots/radiation effects , Root Nodules, Plant/genetics , Root Nodules, Plant/growth & development , Root Nodules, Plant/microbiology , Root Nodules, Plant/radiation effects , Symbiosis
6.
J Radiat Res ; 51(6): 651-6, 2010.
Article in English | MEDLINE | ID: mdl-21116098

ABSTRACT

The mutagenic effects of low-energy ions have been identified by genetic studies for decades. Due to the short penetration distance of ions, however, the underlying mechanism(s) is still not quite clarified. Recently, increasing data have been accumulated concerning the existence and manifestation of radiation induced bystander/abscopal effects in vivo in the whole-organism environment. In this study, the bio-effects and the preliminary mechanisms of low energy ion beam irradiation on Medicago truncatula were investigated. The results show that both development and biochemical parameters, such as seed germination, seedling, superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD) were significantly affected by ion beam irradiation. It was also found that ion beam irradiation significantly increased the ROS generation and DNA strand breaks in Medicago truncatula. To further investigate the mechanism(s) underlying the responses, seeds were treated with dimethyl sulfoxide (DMSO), an effective reactive oxygen species (ROS) scavenger, and the results showed that DMSO treatment effectively rescued the seed germination and seedling rates and the morphological parameters of development, suggesting that ROS might play an essential role in the mechanisms of the bio-effects of ion-beam irradiated Medicago truncatula.


Subject(s)
Medicago truncatula/radiation effects , Seeds/radiation effects , Bystander Effect/radiation effects , Catalase/metabolism , DNA Breaks , DNA, Plant/radiation effects , Dimethyl Sulfoxide/pharmacology , Heavy Ions , Medicago truncatula/drug effects , Medicago truncatula/metabolism , Peroxidase/metabolism , Reactive Oxygen Species/metabolism , Seeds/drug effects , Seeds/metabolism , Signal Transduction/radiation effects , Superoxide Dismutase/metabolism
7.
J Exp Bot ; 59(13): 3509-22, 2008.
Article in English | MEDLINE | ID: mdl-18703494

ABSTRACT

A better knowledge of the nitrogen nutrition of Medicago truncatula at the whole plant level and its modulation by environmental factors is a crucial step to reach a complete understanding of legume nitrogen nutrition. This study was based on the symbiotic system that is the most commonly used by the research community (M. truncatula cv. Jemalong A17 x Rhizobium meliloti strain 2011). Plant nitrogen nutrition was analysed in relation to carbon nutrition, under a range of nitrate concentrations in the nutrient solution and different light conditions. This study shows that this 'model symbiotic association' does not allow the plant to meet its nitrogen requirements, when dinitrogen fixation is the main nitrogen source for plant growth. A strong interaction between nitrogen and carbon nutrition was shown: when plant nitrogen requirements were not sustained, plant leaf area was much affected whereas photosynthesis per unit leaf area remained relatively stable. Both total nitrogen uptake and leaf area increased with increasing nitrate concentration in the nutrient solution; the magnitude of these responses varied according to the light conditions. Interestingly, the plant nitrogen nutrition level remained nearly unaffected by the light conditions. The observed nitrogen-limitation in this 'model symbiotic association' is an important finding for the research community. Based on practical recommendations regarding both the experimental conditions and the phenotypic traits to consider, a methodological framework was proposed to (i) help genomicists to assess plant nitrogen nutrition better, and (ii) assist in the detection of new genetic variants affected for nitrogen uptake in large-scale phenotyping studies.


Subject(s)
Medicago truncatula/physiology , Models, Biological , Nitrogen Fixation , Nitrogen/metabolism , Sinorhizobium meliloti/physiology , Symbiosis , Medicago truncatula/growth & development , Medicago truncatula/radiation effects , Nitrates/metabolism , Photosynthesis , Plant Leaves/growth & development , Plant Leaves/physiology , Plant Leaves/radiation effects
8.
J Exp Bot ; 56(410): 323-36, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15596476

ABSTRACT

GC-MS-based metabolite profiling was used to analyse the response of Medicago truncatula cell cultures to elicitation with methyl jasmonate (MeJa), yeast elicitor (YE), or ultraviolet light (UV). Marked changes in the levels of primary metabolites, including several amino acids, organic acids, and carbohydrates, were observed following elicitation with MeJa. A similar, but attenuated response was observed following YE elicitation, whereas little response was observed following UV elicitation. MeJa induced the accumulation of the triterpene beta-amyrin, a precursor to the triterpene saponins, and LC-MS analysis confirmed the accumulation of triterpene saponins in MeJa-elicited samples. In addition, YE induced a slight, but significant accumulation of shikimic acid, an early precursor to the phenylpropanoid pathway, which was also demonstrated to be YE-inducible by LC-MS analyses. Correlation analyses of metabolite relationships revealed perturbation of the glycine, serine, and threonine biosynthetic pathway, and suggested the induction of threonine aldolase activity, an enzyme as yet uncharacterized from plants. Members of the branched chain amino acid pathway accumulated in a concerted fashion, with the strongest correlation being that between leucine and isoleucine (r2=0.941). While UV exposure itself had little effect on primary metabolites, the experimental procedure, as revealed by control treatments, induced changes in several metabolites which were similar to those following MeJa elicitation. Sucrose levels were lower in MJ- and YE-elicited samples compared with control samples, suggesting that a portion of the effects observed on the primary metabolic pool are a consequence of fundamental metabolic repartitioning of carbon resources rather than elicitor-specific induction. In addition, beta-alanine levels were elevated in all elicited samples, which, when viewed in the context of other elicitation responses, suggests the altered metabolism of coenzyme A and its esters, which are essential in secondary metabolism.


Subject(s)
Medicago truncatula/metabolism , Acetates/pharmacology , Cell Culture Techniques , Cyclopentanes/pharmacology , Gas Chromatography-Mass Spectrometry , Medicago truncatula/chemistry , Medicago truncatula/drug effects , Medicago truncatula/radiation effects , Oxylipins , Plant Growth Regulators/pharmacology , Ultraviolet Rays , Yeasts
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