Browsing by Subject "Flowering"

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    Comprehensive analyses of DNA methylation profile, regulation on flowering, and seed mineral accumulation in Arabidopsis thaliana in response to zinc deficiency
    (2016) Chen, Xiaochao; Ludewig, Uwe
    Zinc (Zn) is an essential micronutrient for plant growth and development, which plays important roles in DNA binding, metabolic, catalytic and transcriptional regulator activities. However, Zn deficiency is a worldwide problem due to its limited bioavailability in soils in many agricultural areas, often as a result of high CaCO3 content and high pH. In addition, phytic acid is able to strongly chelate cations, such as Zn2+, Fe2+, Ca2+ and Mg2+ to form the phytate salts. Phytate cannot be digested by human beings or other monogastric animals due to lack of phytase, an enzyme that can hydrolyze phytate. Therefore, Zn bioavailability in seeds (or grains) is restricted by phytate. Moreover, seed Zn concentration is also reduced by elevated CO2, especially in C3 plants, such as wheat, rice and soybean. Regarding to the crucial roles but limited bioavailability of Zn, here I present a comprehensive analysis on roots, leaves (and flowering) and seeds in response to Zn deficiency in the model plant Arabidopsis thaliana via three experiments. First, I investigated the transcriptional response and whole-genome DNA methylation profile upon Zn deficiency in roots using next-generation sequencing. Ionome analysis on shoots showed that Zn concentration was strongly reduced in Zn deficiency, whereas other nutrients were not affected. Microarray Analysis identified several known Zn-deficiency responsive genes, confirming the effectiveness of Zn deficiency in this work. However, bisulfite sequencing results revealed that DNA methylation was eliminated by Zn deficiency in transposable elements and slightly in gene bodies as well. The DNA demethylation response to nutrient stress was a novel finding, as reversed to previous reports about phosphate stress which accumulated methylation. Surprisingly, further analysis suggested that DNA methylation occurred independent of gene transcription. Nevertheless, non-CpG methylation has a potential impact on flower development in response to Zn deficiency. The second experiment investigated the relationship between rosette size and flowering, and how rosette size and flowering time were regulated by Zn deficiency. Using natural variation population (168 Arabidopsis accessions), I found that flowering time was positively correlated with rosette size in early-flowering accessions but not in late-flowering accessions. Intriguingly, the flowering time was delayed by Zn deficiency in these early-flowering plants and resulting in promotion of vegetative biomass. However, Zn-regulated flowering time was independent of previously reported flowering pathways. Then genome-wide association study identified the underlying candidate gene was FLOWERING LOCUS T (FT) which was strongly inhibited by Zn deficiency in all accessions. Detailed genetic analysis confirmed this result as well. Furthermore, the promotion of leaf size in Zn deficiency was found being contributed by cell proliferation (cell number) but not cell size. Lastly, in the third experiment I was interested in the natural genetic variation in seed Zn concentration, together with iron (Fe) and manganese (Mn), in response to Zn deficiency. Across around 100 accessions, average seed Zn concentration decreased from 47.4 µg g-1 to 31.3 µg g-1 due to Zn deficiency. To identify candidate genes affecting seed Zn, Fe and Mn concentrations, genome-wide association mapping was performed. A candidate gene, inositol 1,3,4-trisphosphate 5/6-kinase 3 gene (ITPK3), was associated which is involved in phytate synthesis pathways. However, loss of this gene in itpk3-1 did neither affect phytate seed levels nor seed Zn, Fe and Mn. Nevertheless, large natural variance of micronutrient seed levels was identified in the population and several accessions maintained high seed Zn despite growth in Zn-deficient conditions. Altogether, this study presents comprehensive analyses in how Arabidopsis adapts to Zn deficiency in regard of root transcription and DNA methylation, flowering and leaf regulation, and seed mineral accumulation. I provided new possibilities of correlation between DNA methylation and gene transcription, which is much more complex than previously reported. I also opened a novel insight into flowering regulation on leaf size, resulting in promotion of vegetative biomass in nutrient deficiency. Substantial natural variation of seed experiment indicated that the evolution process was involved in seed mineral accumulation in Arabidopsis, especially those accessions maintaining Zn concentration in Zn-deficient soils are valuable for further investigations. I believe these findings in Arabidopsis also provide precious knowledge for plant breeders and agronomists who work on crops. 
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    Interplay between nutrition, senescence and cytosine methylation in Arabidopsis thaliana
    (2023) Vatov, Emil; Ludewig, Uwe
    In monocarpic plants, senescence is the last stage of leaf development and usually leads to the death of the organism. Systematic degradation of leaf components provides nutrients for the newly developing flowers and seeds. The physiology and transcriptional changes that occur in A. thaliana during this process are very well documented. However, the involvement of epigenic mechanisms remains to be established. In this study, the role of cytosine methylation in the regulation of monocarpic leaf senescence was examined in A. thaliana. Hypomethylated ddc (drm1/2 cmt3) and hypermethylated ros1 mutants showed consistent senescence-specific phenotypes. Disrupted de-novo methylation resulted in delayed, while disrupted demethylation resulted in earlier flowering and appearance of first symptoms of senescence. Both genotypes executed the senescence program faster than Col-0, with lower leaf:seed and higher C:N ratios. During nitrogen, or phosphorus withdrawal and resupply, nutrient remobilization was not inhibited in the two mutants. However, the plant’s response in terms of changes in shoot and root growth was delayed, or non existent. Furthermore, the impact of N withdrawal on delay of the flowering time was inhibited in the two mutants. These results support involvement of cytosine methylation in stress response signaling and downstream effects on organ development and flowering times. The stress response and senescence specific phenotypes of ddc could be partially due to disrupted WRKY signaling, as loss of methylation in W-box binding sites was prevalent, specifically near the transcription start sites of ORFs, and WRKY18, 25 and 53 appeared to be sensitive towards cytosine methylation. Overall decrease in cytosine methylation levels was observed, as early as the opening of the first flowers, together with a decrease in chlorophyll concentrations and an increase in H2O2 and glucose levels in the wild type Col-0. Inhibition in maintenance methylation in the early stages of reproductive growth is consistent with these observations. A complex interaction between four cytokinins was present as early as flower induction, followed by a mass turnover of bound auxin (IAA) at flower opening, that resulted in near doubling of free IAA at seed development. Plant defense responses were induced thereafter, as an increase in salicylic acid (SA) and camalexin occurred, followed by an increase in jasmonic acid (JA) and abscisic acid (ABA). Active RNA-dependent DNA methylation (RdDM) was indicated by a moderate overrepresentation of hypermethylated CHG and CHH loci, together with partial recovery of total methylation levels at the latest stages during seed maturation. Considering the delayed senescence phenotype of ddc, de-novo methylation via RdDM appears to be involved in initiation and execution of the senescence program. Furthermore, hypomethylation at ROS1 gene regulatory region was related to down regulation of gene expression. As an antagonist of RdDM, together with the early senescence phenotype of ros1, these results strengthen the importance of de-novo methylation for senescence, while active demethylation gets down regulated. Overall, methylation changes were little related to known gene expression changes that are associated with senescence. Limited targeting of WRKY and bZIP binding sites hinders conclusions about senescence specific effects of cytosine methylation in signal transduction networks. Altogether, the present work shines light on the importance of proper maintenance of cytosine methylation for flowering time, nutrient remobilization and senescence, and identifies defined cytosine methylation changes during senescence in a comprehensive physiological framework.