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SRX1668405: GSM2101046: WGBS_tetraploid_2; Arabidopsis thaliana; Bisulfite-Seq
1 ILLUMINA (NextSeq 500) run: 25.9M spots, 7.7G bases, 3.2Gb downloads

Submitted by: NCBI (GEO)
Study: Bisulfite-Seq and RNA-seq profiling of Arabidopsis aneuploids
show Abstracthide Abstract
Aneuploidy refers to gains and/or losses of individual chromosomes from the normal chromosome set. The resulting gene dosage imbalance usually has a deleterious effect on the phenotype, as illustrated in humans by Down Syndrome (trisomy 21) and solid tumor cells, which are typically highly aneuploid. Aneuploidy has been studied for many years in plants and has been a factor contributing to plant chromosome evolution. Nevertheless, there is still relatively little information about how chromosome numerical imbalances affect the molecular constitution of cells and confer altered phenotypes. To investigate these questions we have performed comparative transcriptome (RNA-seq) and methylome (bisulfite-seq) analyses on trisomics (2n+1) of all five chromosomes of Arabidopsis thaliana as well as matched diploids, triploid and tetraploids. Overall design: Trisomics of each of the five Arabidopsis thaliana chromosomes were screened out microscopically at the seedling stage from a population of selfed progeny of a triploid parent using fluorescent-tags on specific chromosomes as markers. The triploid parents are obtained as progeny from a cross between a diploid and a tetraploid. The trisomics were grown in soil and the number of chromosomes was confirmed by counting metaphase chromosomes prepared from flower pistils and by comparative genome hybridization. At least two biological replicates representing each confirmed karyotype (trisomies 1 through 5, diploid, triploid, tetraploid) were used for DNA and RNA isolation. DNA and RNA preparations as well as RNA-seq and bisulfite-seq were carried out according to standard procedures.
Sample: WGBS_tetraploid_2
SAMN04589749 • SRS1366352 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Genomic DNA was isolated from rosette leaves using a Wizard Genomic DNA Purification kit A1120 (Promega, USA). The procedure involves lysis of isolated nuclei, RNase digestion, protein precipitation, centrifugation, precipitation of DNA from the supernatant using isopropanol, followed by a wash step with 70% ethanol. After pelleting the precipitated DNA by centrifugation, it was dried under a vacuum and rehydrated in sterile nuclease free water. genomic DNA was sheared by sonication to generate DNA fragments in the 100-300 bp size range. Bisulfite treatment and library preparation were carried out as described (Feng et al. 2011), except that the EpiTect Fast kit (QIAGEN) was utilized for bisulfite treatment. The resulting libraries were sequenced with Illumina sequencing technology (Illumna NextSeq500 sequencer).
Experiment attributes:
GEO Accession: GSM2101046
Links:
Runs: 1 run, 25.9M spots, 7.7G bases, 3.2Gb
Run# of Spots# of BasesSizePublished
SRR330929625,878,9057.7G3.2Gb2018-06-21

ID:
2394173

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