Transcriptome sequencing and whole genome expression profiling of hexaploid sweetpotato under salt stress
Mohamed Hamed Arisha,
Hesham Aboelnasr,
Muhammad Qadir Ahmad,
Yaju Liu,
Wei Tang,
Runfei Gao,
Hui Yan,
Meng Kou,
Xin Wang,
Yungang Zhang,
Qiang Li
Affiliations
Mohamed Hamed Arisha
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Hesham Aboelnasr
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Muhammad Qadir Ahmad
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Yaju Liu
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Wei Tang
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Runfei Gao
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Hui Yan
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Meng Kou
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Xin Wang
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Yungang Zhang
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Qiang Li
Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District / Key Laboratory of Biology and Genetic Improvement of Sweetpotato, Ministry of Agriculture / Sweetpotato Research Institute, CAAS
Abstract Background Purple-fleshed sweetpotato (PFSP) is one of the most important crops in the word which helps to bridge the food gap and contribute to solve the malnutrition problem especially in developing countries. Salt stress is seriously limiting its production and distribution. Due to lacking of reference genome, transcriptome sequencing is offering a rapid approach for crop improvement with promising agronomic traits and stress adaptability. Results Five cDNA libraries were prepared from the third true leaf of hexaploid sweetpotato at seedlings stage (Xuzi-8 cultivar) treated with 200 mM NaCl for 0, 1, 6, 12, 48 h. Using second and third generation technology, Illumina sequencing generated 170,344,392 clean high-quality long reads that were assembled into 15,998 unigenes with an average length 2178 base pair and 96.55% of these unigenes were functionally annotated in the NR protein database. A number of 537 unigenes failed to hit any homologs which may be considered as novel genes. The current results indicated that sweetpotato plants behavior during the first hour of salt stress was different than the other three time points. Furthermore, expression profiling analysis identified 4, 479, 281, 508 significantly expressed unigenes in salt stress treated samples at the different time points including 1, 6, 12, 48 h, respectively as compared to control. In addition, there were 4, 1202, 764 and 2195 transcription factors differentially regulated DEGs by salt stress at different time points including 1, 6, 12, 48 h of salt stress. Validation experiment was done using 6 randomly selected unigenes and the results was in agree with the DEG results. Protein kinases include many genes which were found to play a vital role in phosphorylation process and act as a signal transductor/ receptor proteins in membranes. These findings suggest that salt stress tolerance in hexaploid sweetpotato plants may be mainly affected by TFs, PKs, Protein Detox and hormones related genes which contribute to enhance salt tolerance. Conclusion These transcriptome sequencing data of hexaploid sweetpotato under salt stress conditions can provide a valuable resource for sweetpotato breeding research and focus on novel insights into hexaploid sweetpotato responses to salt stress. In addition, it offers new candidate genes or markers that can be used as a guide to the future studies attempting to breed salt tolerance sweetpotato cultivars.