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Closterium peracerosum-strigosum-littorale complex

ABSTRACT: Transcriptomics of Closterium peracerosum-strigosum-littorale complex

PROVIDER: PRJNA296352 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR2456790.fastq.gz	Fastqsanger.gz
	SRR2456791.fastq.gz	Fastqsanger.gz
	SRR2456792.fastq.gz	Fastqsanger.gz
	SRR2456783.fastq.gz	Fastqsanger.gz
	SRR2456793.fastq.gz	Fastqsanger.gz

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Closterium peracerosum-strigosum-littorale complex

Project description:Whole genome sequencing of Closterium peracerosum-strigosum-littorale complex.

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Closterium peracerosum-strigosum-littorale complex strain:naga37s-1

Project description:Transcriptome analyses of homothallic Closterium peracerosum-strigosum-littorale complex

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Closterium peracerosum-strigosum-littorale complex

Project description:Detection and evaluation of mating-type specific region using progenies of Closterium peracerosum-strigosum-littorale complex.

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Closterium peracerosum-strigosum-littorale complex strain:NIES-67 and NIES-68

Project description:Transcriptome analyses of heterothallic Closterium peracerosum-strigosum-littorale complex

| PRJDB3387 | ENA

Genome and Transcriptome analysis for Closterium peracerosum-strigosum-littorale complex

Project description:Genome and Transcriptome analysis for Closterium peracerosum-strigosum-littorale complex

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Closterium peracerosum-strigosum-littorale complex strain:NIES-67 and NIES-68

Project description:Transcriptome analyses of R5, which is a transformant expressing CpMinus1, originated from NIES-67 of Closterium peracerosum-strigosum-littorale complex

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Closterium peracerosum-strigosum-littorale complex

Project description:Transcriptome of CpMinus1 KO in comparison with plus and minus strains.

| PRJDB12708 | ENA

Extensive Copy Number Variation Explains Genome Size Variation in the Unicellular Zygnematophycean Alga, Closterium peracerosum-strigosum-littorale Complex.

Project description:Genome sizes are known to vary within and among closely related species, but the knowledge about genomic factors contributing to the variation and their impacts on gene functions is limited to only a small number of species. This study identified a more than 2-fold heritable genome size variation among the unicellular Zygnematophycean alga, Closterium peracerosum-strigosum-littorale (C. psl.) complex, based on short-read sequencing analysis of 22 natural strains and F1 segregation analysis. Six de novo assembled genomes revealed that genome size variation is largely attributable to genome-wide copy number variation (CNV) among strains rather than mating type-linked genomic regions or specific repeat sequences such as rDNA. Notably, about 30% of genes showed CNV even between strains that can mate with each other. Transcriptome and gene ontology analysis demonstrated that CNV is distributed nonrandomly in terms of gene functions, such that CNV was more often observed in the gene set with stage-specific expression. Furthermore, in about 30% of these genes with CNV, the expression level does not increase proportionally with the gene copy number, suggesting presence of dosage compensation, which was overrepresented in genes involved in basic biological functions, such as translation. Nonrandom patterns in gene duplications and corresponding expression changes in terms of gene functions may contribute to maintaining the high level of CNV associated with extensive genome size variation in the C. psl. complex, despite its possible detrimental effects.

| S-EPMC10407611 | biostudies-literature

Concanavalin A Disrupts the Release of Fibrous Material Necessary for Zygote Formation of a Unicellular Charophycean Alga, Closterium peracerosum-strigosum-littorale Complex.

Project description:The Closterium peracerosum-strigosum-littorale (C. psl.) complex is the best characterized charophycean alga with respect to the processes of sexual reproduction. We examined the effect of concanavalin A (Con A) on physiological and ultrastructural changes during the conjugation of the C. psl. complex. Two heterothallic gametangial cells formed a sexual pair as usual; however, the release of gametes was completely blocked by the addition of Con A. Fluorescein isothiocyanate-labeled Con A bound to the outermost layer of the conjugation papillae of paired cells. In the absence of Con A, the disruption of outer cell walls on the conjugation papillae and the secretion of fibrous materials from the conjugation papillae were observed using a transmission electron microscope, but Con A-treated cells did not show these changes. Instead, a highly electron-dense layer was observed in the outermost papillae, and the excess fibrous materials remained at the inside of the layer. These results suggest that an unknown molecule(s) recognized by Con A is essential for the diffusion of fibrous materials at the conjugation papillae, which is an indispensable step for gamete release during conjugation of the C. psl. complex.

| S-EPMC4942458 | biostudies-literature

CRISPR/Cas9-based knockouts reveal that CpRLP1 is a negative regulator of the sex pheromone PR-IP in the Closterium peracerosum-strigosum-littorale complex.

Project description:Heterothallic strains of the Closterium peracerosum-strigosum-littorale (C. psl.) complex have two sexes, mating-type plus (mt+) and mating-type minus (mt-). Conjugation between these two sexes is regulated by two sex pheromones, protoplast-release-inducing protein (PR-IP) and PR-IP Inducer, which are produced by mt+ and mt- cells, respectively. PR-IP mediates the release of protoplasts from mt- cells during mating. In this study, we examined the mechanism of action of CpRLP1 (receptor-like protein 1), which was previously identified in a cDNA microarray analysis as one of the PR-IP-inducible genes. Using CRISPR/Cas9 technology, we generated CpRLP1 knockout mutants in mt- cells of the C. psl. complex. When the knockout mt- cells were mixed with wild-type mt+ cells, conjugation was severely reduced. Many cells released protoplasts without pairing, suggesting a loss of synchronization between the two mating partners. Furthermore, the knockout mutants were hypersensitive to PR-IP. We conclude that CpRLP1 is a negative regulator of PR-IP that regulates the timing of protoplast release in conjugating C. psl. cells. As the first report of successful gene knockout in the class Charophyceae, this study provides a basis for research aimed at understanding the ancestral roles of genes that are indispensable for the development of land plants.

| S-EPMC5736609 | biostudies-literature

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