IC4R013-RNA-Seq-2012-22537016

Project Title

• Comparative transcriptome analysis of transporters, phytohormone and lipid metabolism pathways in response to arsenic stress in rice (Oryza sativa)

The Background of This Project

• Arsenic (As) contamination of rice (Oryza sativa) is a worldwide concern and elucidating the molecular mechanisms of As accumulation in rice may provide promising solutions to the problem. Previous studies using microarray techniques to investigate transcriptional regulation of plant responses to As stress have identified numerous differentially expressed genes. However, little is known about the metabolic and regulatory network remodelings, or their interactions with microRNA (miRNA) in plants upon As(III) exposure. In this project, the researchers used Illumina sequencing to acquire global transcriptome alterations and miRNA regulation in rice under As(III) treatments of varying lengths of time and dosages.

Plant Culture & Treatment

• The rice cultivar Nipponbare (Oryza sativa L. ssp japonica) was used in this study because this cv genome has been well sequenced. Seeds were sterilized in 30% H2O2 and germinated for 3 d at 37℃. Seedlings were grown inhalf-strength Hoagland nutrient solution at 28℃ day ⁄ 25℃ night with a photoperiod of 16 h light (09:00–00:59 h) and 8 h night (01:00–08:59 h) in the glasshouse. Our pre-experiments had shown that the growth of rice seedlings was strongly inhibited by 100 lM sodium arsenite (As(III)) stress when the seedlings were treated with a series of As(III) concentrations from 10 to 100 lM. Therefore, for the As(III) treatments, 14-d-old rice seedlings were exposed to As(III) (20 and 80 lM) at 09:00 h, and materials were harvested at 0, 6 and 24 h after treatment. For each treatment, pooling of roots or shoots of the three individual plants in a sample was conducted as described previously. The samples were frozen in liquid nitrogen immediately and stored at -80℃ until use.
• Comparisons (Supporting Information, Fig. S1) between the untreated samples (untreated root and shoot were labeled as CKR and CKS, respectively) and As(III) treated samples (LSR and LLR refer to 20 lM As(III)-treated roots for 6 and 24 h, respectively; HSR and HLR refer to 80 lM As(III)-treated roots for 6 and 24 h, respectively; LSS and LLS refer to 20 lM As(III)-treated shoots for 6 and 24 h, respectively; HSS and HLS refer to 80 lM As(III)-treated shoots for 6 and 24 h, respectively) were performed for different time periods and dosages.

Illumina Sequencing

• Total RNA was extracted using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s instructions and was treated with RNase-free DNase I (New England Biolabs, Inc. Ipswich, MA, USA) to remove contaminated genomic DNA. mRNA was isolated from total RNA using Dynabeads oligo(dT) (Invitrogen). First- and second-strand cDNA was generated using Superscript II reverse transcriptase (Invitrogen) and random hexamer primers. Double stranded cDNA was fragmented by nebulization and used for mRNA library construction according to the Illumina paired-end sample preparation protocol, using custom multiplex-indexed Solexa adaptors and sequenced as 75x2 using the Illumina GA Genome Analyzer paired-end pipeline. The original data set was deposited in the NCBI GEO database (access no. GSE36696).

Labs working on this Project

• State Key Laboratory of Biocontrol and Guangdong Key Laboratory of Plant Resources, School of Life Sciences, Sun Yat-sen University, Guangzhou 510275, China
• Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100029, China

Corresponding Author

• Wen-sheng Shu: shuws@mail.sysu.edu.cn; & Song-nian Hu: husn@big.ac.cn