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ERX11684766: RNA sequencing of control and OsADF1/6/9 triple knockout mutant in mature rice anthers (Oryza sativa japonica)
1 ILLUMINA (Illumina NovaSeq 6000) run: 36.4M spots, 7.4G bases, 2.1Gb downloads

Design: RNA sequencing of control and OsADF1/6/9 triple knockout mutant in mature rice anthers (Oryza sativa japonica)
Submitted by: EBI (European Bioinformatics Institute)
Study: RNA sequencing of control and OsADF1/6/9 triple knockout mutant in mature rice anthers (Oryza sativa japonica)
show Abstracthide Abstract
We created a triple loss-of-function/knockout mutant targeting three rice genes simultaneously. The three selected genes are as follows: OsADF1 (LOC_Os02g44470), OsADF6 (LOC_Os04g46910), and OsADF9 (LOC_Os07g30090). These three ADFs are strongly transcriptional expressed in the rice mature anthers (stages 13) and bi-/tricelluler pollen. The triple mutant of these OsADFs does not produce self-fertilizing seeds due to the short length of the pollen tube (male-sterile). This data is about mature anther transcriptome data about the triple mutant of OsADFs (ADFmT). We sampled mature anther for the analysis.
Sample: OsADF1/6/9-2
SAMEA114644353 • ERS17047941 • All experiments • All runs
Library:
Name: OsADF1/6/9-2_p
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: Oligo-dT
Layout: PAIRED
Construction protocol: Anthers that include bicellular and tricellular stages of pollen were collected (11 to 13 stages of Anthers). Seeds of japonica rice cv. Dongjin was sterilized with 50% sodium hypochlorite and germinated in MS zero media in an incubator (14-h light/10-h dark, 28 °C (day)/22 °C (night), humidity 80%). After 1 week of germination, seedlings were transferred and grown in the greenhouse for 4 weeks under growth chamber conditions and transferred to the field. Mature anthers were frozen directly in Liquid nitrogen and finely ground using mortar. Grounded samples were homogenized using TRI reagents (RNAiso, Takara) and BCP (1-bromo-3-chloropropane). DNA, RNA, and protein layers were separated by centrifugation. Then, total RNA was extracted using the RNeasy Mini Kit (QIAGEN). The sequencing library is prepared by random fragmentation of the DNA or cDNA sample, followed by 5' and 3' adapter ligation. Alternatively, \"tagmentation\" combines the fragmentation and ligation reactions into a single step that greatly increases the efficiency of the library preparation process. Adapter-ligated fragments are then PCR amplified and gel purified.
Runs: 1 run, 36.4M spots, 7.4G bases, 2.1Gb
Run# of Spots# of BasesSizePublished
ERR1230782536,388,2867.4G2.1Gb2024-07-20

ID:
33931457

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