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SRX5578315: GSM3688041: 26-3-1_RNAseq; Zea mays; RNA-Seq
4 ILLUMINA (NextSeq 500) runs: 45.1M spots, 3.4G bases, 1.1Gb downloads

Submitted by: NCBI (GEO)
Study: Changes in the maize (B73) 1-cm primary root growth zone transcriptome induced by mild (-0.03 MPa) or severe water-deficit stress (-1.6 MPa)
show Abstracthide Abstract
Transcriptome sequencing (RNA-seq) was used to profile genome-wide transcript abundance in the primary root growth zone (PRGZ) of maize seedlings grown in different water deficit treatments: well-watered (-0.02 MPa), mild water deficit stress (-0.3 MPa), or severe water deficit stress (-1.6 MPa). For each water deficit treatment, the PRGZ transcriptome was profiled at 26 hours after initiation of the water deficit treatment. By comparing the abundance of each transcript under mild or severe water deficit stress relative to its abundance under well-watered conditions, we identified transcripts that are differentially regulated in the PRGZ in response to the two levels of water deficit stress. Overall design: For each of the three treatments (well-watered, mild water deficit, and severe water deficit), three biological replicates consisting of 5 x 1-cm primary root growth zone segments of maize seedlings were examined by RNA-seq.
Sample: 26-3-1_RNAseq
SAMN11259665 • SRS4540174 • All experiments • All runs
Organism: Zea mays
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was extracted using the RNEasy Plant Mini Kit (Qiagen, Carlsbad, CA) and treated with Turbo DNase (Life Technologies, Carlsbad, CA) to remove contaminating genomic DNA. Libraries were prepared according to Illumina's instructions accompanying the DNA Sample Kit (Part# 0801-0303). Libraries were prepared using the NEBNext mRNA Library Prep Master Mix Set for Illumina and according to kit's instructions. Briefly, polyA mRNA was purified from 1 µg total RNA using the Dynabeads mRNA DIRECT Purification kit. After mRNA fragmentation and cDNA synthesis, adaptors were ligated and library fragments of ~100 bp were selected using AMPure XP beads. DNA fragments were PCR amplified with Illumina primers for 10 cycles. Libraries were sequenced on the Illumina NextSeq 500 platform following the manufacturer's protocols. RNA-seq each library was split into four parts for sequencing on independent lanes so as to remove any lane bias
Experiment attributes:
GEO Accession: GSM3688041
Links:
Runs: 4 runs, 45.1M spots, 3.4G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR878850811,263,630840.7M286.9Mb2019-04-30
SRR878850911,042,838824.4M280.7Mb2019-04-30
SRR878851011,376,254849.2M289.8Mb2019-04-30
SRR878851111,408,989851.9M290.5Mb2019-04-30

ID:
7527648

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