Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR20747204_1.fastq.gz | Fastqsanger.gz | |||
| SRR20747204_2.fastq.gz | Fastqsanger.gz | |||
| SRR20747205_1.fastq.gz | Fastqsanger.gz | |||
| SRR20747205_2.fastq.gz | Fastqsanger.gz | |||
| SRR20747206_1.fastq.gz | Fastqsanger.gz |
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Project description:A functional gene microarray was developed and used to investigate phytoplankton community composition and gene expression in the English Channel. Genes encoding the CO2 fixation enzyme RuBisCO (rbcL) and the nitrate assimilation enzyme nitrate reductase (NR) representing several major groups of phytoplankton were included as oligonucleotide probes on the 'phytoarray'. Five major groups of eukaryotic phytoplankton that possess the Type 1D rbcL gene were detected, both in terms of presence (DNA) and activity (rbcL gene expression). Changes in relative signal intensity among the Type 1D rbcL probes indicated a shift from diatom dominance in the spring bloom to dominance by haptophytes and flagellates later in the summer. Because of the limitations of a smaller database, NR probes detected fewer groups, but due to the greater diversity among known NR sequences, NR probes provided higher phylogenetic resolution than did rbcL probes, and identified two uncultivated diatom phylotypes as the most abundant (DNA) and active (NR gene expression) in field samples. Unidentified chlorophytes and the diatom Phaeodactylum tricornutum were detected at both the DNA and cDNA (gene expression) levels. The reproducibility of the array was evaluated in several ways and future directions for further improvement of probe development and sensitivity are outlined. The phytoarray provides a relatively high resolution, high throughput approach to assessing phytoplankton community composition in marine environments. Keywords: seawater natural assemblages, functional gene expression
2008-09-12 | GSE12742 | GEO
Project description:A functional gene microarray was developed and used to investigate phytoplankton community composition and gene expression in the English Channel. Genes encoding the CO2 fixation enzyme RuBisCO (rbcL) and the nitrate assimilation enzyme nitrate reductase (NR) representing several major groups of phytoplankton were included as oligonucleotide probes on the 'phytoarray'. Five major groups of eukaryotic phytoplankton that possess the Type 1D rbcL gene were detected, both in terms of presence (DNA) and activity (rbcL gene expression). Changes in relative signal intensity among the Type 1D rbcL probes indicated a shift from diatom dominance in the spring bloom to dominance by haptophytes and flagellates later in the summer. Because of the limitations of a smaller database, NR probes detected fewer groups, but due to the greater diversity among known NR sequences, NR probes provided higher phylogenetic resolution than did rbcL probes, and identified two uncultivated diatom phylotypes as the most abundant (DNA) and active (NR gene expression) in field samples. Unidentified chlorophytes and the diatom Phaeodactylum tricornutum were detected at both the DNA and cDNA (gene expression) levels. The reproducibility of the array was evaluated in several ways and future directions for further improvement of probe development and sensitivity are outlined. The phytoarray provides a relatively high resolution, high throughput approach to assessing phytoplankton community composition in marine environments. Keywords: seawater natural assemblages, functional gene expression Two functional genes, nitrate reductase and RuBisCO, 4 - 8 replicate features per array
2010-06-19 | E-GEOD-12742 | biostudies-arrayexpress
Project description:The nuclear-encoded chloroplastic RNA-binding protein CP29A is important for the cold response in Arabidopsis thaliana. Knockout mutations in this plant species lead to a bleaching phenotype in the newly developing tissue. Important for the function of AtCP29A is a long prion like domain, which is located between the two RNA Recognition Motifs (RRM). In contrast, the CP29A variant of N. tabacum contains only a short linker between the two RRMs. Knockout mutants of this gene show a phenotype when analysed by pulse amplitude modulation (PAM) fluorometry. In this study, we analysed the differentially expressed chloroplast genes of the NtCP29A mutant compared to the wild-type of N. tabacum (Petit havana) under normal (24°C) and under cold (12°C) growth conditions. While no gene was significantly deregulated under normal conditions, RbcL proved to be the only gene that was significantly downregulated under cold conditions in the mutant.
2024-11-21 | GSE248582 | GEO
Project description:Chromophytic phytoplankton diversity using rbcL gene Raw sequence reads
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Project description:West Pacific Ocean rbcL gene diversity Raw sequence reads
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Project description:West Pacific Ocean rbcL gene diversity Raw sequence reads
| PRJNA557821 | ENA