PRJNA153619: Comparative transcriptome analysis of transporters, phytohormone and lipid metabolism pathways in response to arsenic stress in rice (Oryza Sativa L.)
概要: Arsenic (As) is a carcinogenic metalloid that is a contaminant widely polluting rice paddy soils around the world. In order to gain better insight into molecular mechanism of rice exposed to As(III) stress, we used next-generation sequencing technology to acquire global transcriptome alteration and miRNA regulation in rice upon As(III) treatments. Our results suggest time course and As(III)-dosing treatments were devised. Cluster analyses show that root and shoot samples were differentially grouped. For roots, sub-clusters were more distinct in the dosage course whereas for shoots they were most recognizable for the time course treatments. Other than the significantly regulated gene expression in the heavy metal-responsive sulfur and glutathione metabolism pathways, the expression of genes related to heavy metal transportation, jasmonate biosynthesis and signaling pathways, lipid metabolism and gene transcription were sharply regulated, indicating that rice allocates energy and resources from growth to stress response under As(III) stress. In addition to the detection of previously identified stress-related miRNAs, we further discovered 36 new As(III)-responsive miRNAs. These results expand our understanding of As(III) stress mechanism to the As(III)-responsive mRNA and miRNA transcriptomes, which provide a foundation for subsequent functional research.
Seedlings were grown in 1/2 Hoagland nutrient solution at 28°C day/ 25°C night with a photoperiod of 16 h light (9:00-0:59) and 8 h night (1:00-8:59) in the green house.
处理方案:
For As(III) treatments, 14-d-old rice seedlings were exposed to sodium arsenite (20 and 80 μm) at 9:00, and materials were harvested at 0, 6 and 24 h after treatment.
提取方案:
Total RNA was extracted using TRIzol reagent (Invitrogen) following the manufacturer’s instructions and was treated with RNase-free DNase I (New England Biolabs) to remove contaminated genomic DNA. mRNA was isolated from total RNA using Dynabeads oligo(dT) (Invitrogen). First- and second-strand cDNA were generated using Superscript II reverse transcriptase (Invitrogen) and random hexamer primers.
建库方案:
Double-stranded cDNA was fragmented by nebulization and used for mRNA library construction according to the illuminaIllumina paired-end sample preparation protocol, using custom multiplex indexed Solexa adaptors and sequenced as 75 × 2 using the Illumina GA Genome Analyzer paired-end pipeline.
测序信息
分子类型:
poly(A)+ RNA
库的片段类型:
PAIRED
库的链类型:
-
测序平台:
ILLUMINA
测序仪型号:
Illumina Genome Analyzer IIx
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Unspecific
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文章
Comparative transcriptome analysis of transporters, phytohormone and lipid metabolism pathways in response to arsenic stress in rice (Oryza sativa).