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SRX13244400: GSM5706347: OsTOPBP1C-overexpressor_0h_1; Oryza sativa Japonica Group; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 19.9M spots, 6G bases, 1.9Gb downloads

Submitted by: NCBI (GEO)
Study: The interfering transcription activator-like effector DR16 and OsSOG1 attenuates OsTOPBP1C-activated rice bacterial blight resistance
show Abstracthide Abstract
we monitored the responsive changes of rice genes at 0 and 6 hours across Xoo pathotype GIV infection in Nipponbare (NIP), ostopbp1c mutant and OsTOPBP1C-overexpressor by RNA sequencing. These findings provide new insights for directly identifying iTALEs-targeted resistance gene and the regulatory roles of OsTOPBP1C in rice-Xoo interactions. Overall design: Examination of the responsive changes of rice genes at 0 and 6 hours under Xoo pathotype GIV treatment in Nipponbare (NIP), ostopbp1c mutant and OsTOPBP1C-overexpressor by RNA sequencing
Sample: OsTOPBP1C-overexpressor_0h_1
SAMN23481382 • SRS11167819 • All experiments • All runs
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Every sample was pooled with infected leaves collected from 15 plants in one plot to diminish the individual environment differences.Total RNA from the mentioned samples were extracted using Trizol reagent (Invitrogen, USA) according to the manufacturer's recommendation. NEB Next Poly(A) mRNA Magnetic Isolation Module (NEB) kit was used to enrich the poly(A) tailed mRNA molecules from 1 μg total RNA. The mRNA was fragmented into ~200 base pair pieces. The first-strand cDNA was synthesized from the mRNA fragments reverse transcriptase and random hexamer primers, and then the second-strand cDNA was synthesized using DNA polymerase I and RNaseH. The end of the cDNA fragment was subjected to an end repair process that included the addition of a single “A” base, followed by ligation of the adapters. Products were purified and enriched by polymerase chain reaction (PCR) to amplify the library DNA. The final libraries were quantified using KAPA Library Quantification kit (KAPA Biosystems, South Africa) and an Agilent 2100 Bioanalyzer. After quantitative reverse transcription-polymerase chain reaction (RT-qPCR) validation, libraries were subjected to paired-end sequencing with pair end 150-base pair reading length on an Illumina NovaSeq sequencer (Illumina)
Experiment attributes:
GEO Accession: GSM5706347
Links:
Runs: 1 run, 19.9M spots, 6G bases, 1.9Gb
Run# of Spots# of BasesSizePublished
SRR1705541419,899,5556G1.9Gb2024-01-01

ID:
18121649

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