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SRX2273231: GSM2362486: 2nd leaf, DAH44_Replicate2; Oryza sativa Japonica Group; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 19.5M spots, 3.9G bases, 2.2Gb downloads

Submitted by: NCBI (GEO)
Study: Fundamental molecular bases for differential transcriptional programs of top leaves during grain-filling in rice
show Abstracthide Abstract
Flag (FL) and second leaves (SL) in rice show differential aging patterns during monocarpic senescence. Coordination of aging programs in the top leaves is important for effective grain-filling. However, molecular bases for differential aging programs in the top leaves have not been systematically explored in rice. Here, we performed mRNA-sequencing of FL and SL at six time points during the grain-filling period. mRNA expression data revealed 6,365 genes showing aging-dependent expression changes in FL and/or SL. Of them, while 3047 genes showed shared aging-dependent expression patterns between FL and SL, 3058 genes showed differential expression patterns, which were classified into 5 major groups (G1-5) based on their differential expression patterns. Of the groups, G3 representing amino acid (AA) transport showed consistent differential age-dependent expression patterns in independent samples, whereas the other groups showed inconsistent differential expression patterns. Moreover, of AA transporters (AATs) in G3, long-distance AATs showed invariant differential age-dependent expression patterns after panicle removal, consistent to panicle removal-invariant differential nitrogen contents between FL and SL, known to be associated with protein concentration in grains. Our results suggest that long-distance AA transport is an invariant core transcriptional program of differential aging in rice top leaves for nitrogen remobilization during grain-filling. Overall design: mRNA expression profiles of the flag leaf and 2nd leaf of Oryza Sativa during grain filling (Day After Heading, DAH, 4-44) were examined by Illumina Hi-seq 2500.
Sample: 2nd leaf, DAH44_Replicate2
SAMN05947096 • SRS1764318 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Rice leaf tissue was ground using a mortar and pestle, and total RNA was extracted from ~100 mg of tissue using RNeasy Plant Mini Kit (Qiagen). Total RNA integrity was confirmed using the Agilent Technologies 2100 BioAnalyzer (RNA integrity number >8.0). Poly(A) mRNA isolation from total RNA and fragmentation were performed using the Illumina Truseq Stranded mRNA LT Sample Prep Kit with poly-T oligo-attached magnetic beads, according to the manufacturer’s instructions. Libraries were prepared for multiplex sequencing using Illumina Truseq Stranded mRNA LT Sample Prep Kit, according to the manufacturer’s protocol.
Experiment attributes:
GEO Accession: GSM2362486
Links:
Runs: 1 run, 19.5M spots, 3.9G bases, 2.2Gb
Run# of Spots# of BasesSizePublished
SRR445726519,506,7083.9G2.2Gb2017-09-22

ID:
3334927

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