Publications by authors named "Daichi Susaki"

Article Synopsis
  • In angiosperms, epigenetic profiles crucial for genomic imprinting are set up before fertilization, but the connection between these modifications and gene expression is not fully clear.
  • This research categorized imprinted genes in rice endosperm into 'persistent' and 'stage-specific' types based on a transcriptome analysis over time and found differences in the levels of epigenetic modifications between them.
  • The study showed that maternal allele activation in maternally expressed imprinted genes is linked to DNA demethylation, while paternally expressed genes with gene body methylation are silenced through similar processes and associated with specific genetic motifs.
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In pollen and pollen tubes, immotile sperm cells are enclosed by an inner vegetative plasma membrane (IVPM), a single endomembrane originating from the vegetative-cell plasma membrane. It is widely believed that sperm cells must be removed from the IVPM prior to gamete associations and fusions; however, details of the timing and morphological changes upon IVPM dissociation remain elusive. Here, we report a rapid IVPM breakdown immediately before double fertilization in .

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Pollen tube attraction is a key event of sexual reproduction in flowering plants. In the ovule, two synergid cells neighboring the egg cell control pollen tube arrival via the active secretion of attractant peptides such as AtLURE1 and XIUQIU from the filiform apparatus (FA) facing toward the micropyle. Distinctive cell polarity together with longitudinal F-actin and microtubules are hallmarks of the synergid cell in various species, though the functions of these cellular structures are unclear.

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Nutrient transfer from mother to embryo is essential for reproduction in viviparous animals. In the viviparous teleost Xenotoca eiseni (family Goodeidae), the intraovarian embryo intakes the maternal component secreted into the ovarian fluid via the trophotaenia. Our previous study reported that the epithelial layer cells of the trophotaenia incorporate a maternal protein via vesicle trafficking.

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The female gametophytes of angiosperms contain cells with distinct functions, such as those that enable reproduction via pollen tube attraction and fertilization. Although the female gametophyte undergoes unique developmental processes, such as several rounds of nuclear division without cell plate formation and final cellularization, it remains unknown when and how the cell fate is determined during development. Here, we visualized the living dynamics of female gametophyte development and performed transcriptome analysis of individual cell types to assess the cell fate specifications in Arabidopsis thaliana.

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Article Synopsis
  • Nuclear fusion in flowering plants occurs three times during sexual reproduction, including once in female gametogenesis and twice in double fertilization.
  • GEX1 is a conserved membrane protein crucial for these nuclear fusion processes, comparable to the yeast protein Kar5, indicating its role as a karyogamy factor.
  • GEX1-deficient female gametophytes show unfused polar nuclei, suggesting GEX1 is vital for nuclear membrane fusion, as evidenced by observations from electron microscopy and live-cell imaging.
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Epigenetic marks are reprogrammed in the gametes to reset genomic potential in the next generation. In mammals, paternal chromatin is extensively reprogrammed through the global erasure of DNA methylation and the exchange of histones with protamines. Precisely how the paternal epigenome is reprogrammed in flowering plants has remained unclear since DNA is not demethylated and histones are retained in sperm.

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Fertilization comprises a complex series of cellular processes leading to the fusion of a male and female gamete. Many studies have been carried out to investigate each step of fertilization in plants; however, our comprehensive understanding of all the sequential events during fertilization is still limited. This is largely due to difficulty in investigating events in the female gametophyte, which is deeply embedded in the maternal tissue.

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Mature seed dormancy is a vital plant trait that prevents germination out of season. In , the trait can be maternally regulated but the underlying mechanisms sustaining this regulation, its general occurrence and its biological significance among accessions are poorly understood. Upon seed imbibition, the endosperm is essential to repress the germination of dormant seeds.

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In angiosperms, pollen tubes carry two sperm cells toward the egg and central cells to complete double fertilization. In animals, not only sperm but also seminal plasma is required for proper fertilization. However, little is known regarding the function of pollen tube content (PTC), which is analogous to seminal plasma.

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The female gametophytes of many flowering plants contain one egg cell, one central cell, two synergid cells and three antipodal cells with respective morphological characteristics and functions. These cells are formed by cellularization of a multinuclear female gametophyte. However, the dynamics and mechanisms of female gametophyte development remain largely unknown due to the lack of a system to visualize directly and manipulate female gametophytes in living material.

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In mammals and plants, parental genomic imprinting restricts the expression of specific loci to one parental allele. Imprinting in mammals relies on sex-dependent de novo deposition of DNA methylation during gametogenesis but a comparable mechanism was not shown in plants. Rather, paternal silencing by the maintenance DNA methyltransferase 1 (MET1) and maternal activation by the DNA demethylase DEMETER (DME) cause maternal expression.

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In flowering plants, double fertilization is normally accomplished by the first pollen tube, with the fertilized ovule subsequently inhibiting the attraction of a second pollen tube. However, the mechanism of second-pollen-tube avoidance remains unknown. We discovered that failure to fertilize either the egg cell or the central cell compromised second-pollen-tube avoidance in Arabidopsis thaliana.

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DNA methylation maintains genome stability and regulates gene expression [1]. In mammals, DNA methylation is reprogrammed in the germline from one generation to the next [2]. In plants, it was considered that patterns of DNA methylation are stably maintained through sexual reproduction [3-6].

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In Arabidopsis, DEMETER (DME) DNA demethylase contributes to reprogramming of the epigenetic state of the genome in the central cell. However, other aspects of the active DNA demethylation processes remain elusive. Here we show that Arabidopsis SSRP1, known as an HMG domain-containing component of FACT histone chaperone, is required for DNA demethylation and for activation and repression of many parentally imprinted genes in the central cell.

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Background And Aims: During sexual reproduction in higher angiosperms, the pollen tubes are directed to the ovules in the pistil to deliver sperm cells. This pollen tube attraction is highly species specific, and a group of small secreted proteins, TfCRPs, are necessary for this process in Torenia fournieri.

Methods: A candidate pollen tube attractant protein in Torenia concolor, a related species of T.

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Article Synopsis
  • For over 140 years, scientists believed that pollen tubes in flowering plants were guided by attractants from ovules, but concrete evidence for a specific molecule was lacking.
  • Recent research has identified secreted cysteine-rich polypeptides (CRPs) from synergid cells as key attractants in the final stage of pollen tube guidance.
  • In experiments with the plant Torenia fournieri, two specific CRPs, named LUREs, were shown to effectively attract pollen tubes, and blocking these molecules reduced attraction, confirming their role as the signaling attractants.
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