Project description:Purpose: Brassica. juncea is vulnerable to abiotic stresses at specific stages in its life cycle. However, till date no attempts have been made to elucidate the genome-wide changes in the transcriptome of B. juncea subjected to either high temperature or drought stress. Hence, to gain global insights into genes, transcription factors and kinases regulated by these stresses and to provide basic information on coding transcripts that are associated with traits of agronomic importance, we utilized a combinatorial approach of next generation sequencing and de novo assembly to discover B. juncea transcriptome associated with high temperature and drought. Results: We constructed and sequenced three transcriptome libraries namely Brassica control (BC), Brassica high temperature stress (BHS) and Brassica drought stress (BDS) from control, high temperature treated and drought treated seedlings of Brassica juncea. More than 180 million purity filtered reads were generated which were processed through quality parameters and high quality reads were assembled de-novo using SOAPde-novo assembler. A total of 77750 unique transcripts were identified out of which 69,245 (89%) were annotated with high confidence. We established a subset of 19110 transcripts, which were differentially regulated by either high temperature and/or drought stress. Furthermore, 886 and 2834 transcripts that code for transcription factors and kinases, respectively, were also identified. Investigation of identified transcription factors revealed that 92 responded to high temperature, 72 exhibited alterations in expression during drought stress, and 60 were commonly associated with both the stresses. Similarly, 217, 259 and 193 kinases were responsive to high temperature, drought or both stresses, respectively. Maximum number of up-regulated transcription factors in high temperature and drought stress belonged to heat shock factors (HSFs) and dehydration responsive element-binding (DREB) families respectively. We also identified 239 metabolic pathways, which were perturbed during high temperature and drought treatments. Analysis of gene ontologies associated with differentially regulated genes forecasted their involvement in diverse biological processes. Conclusions: Our study provides first comprehensive discovery of B. juncea transcriptome under high temperature and drought stress conditions. Transcriptome resources generated in this study will enhance our understanding on the molecular mechanisms involved in defining the response of B. juncea against two important abiotic stresses. Furthermore this information would benefit designing of efficient crop improvement strategies for tolerance against conditions of high temperature regimes and water scarcity.

Project description:Purpose: Brassica. juncea is vulnerable to abiotic stresses at specific stages in its life cycle. However, till date no attempts have been made to elucidate the genome-wide changes in the transcriptome of B. juncea subjected to either high temperature or drought stress. Hence, to gain global insights into genes, transcription factors and kinases regulated by these stresses and to provide basic information on coding transcripts that are associated with traits of agronomic importance, we utilized a combinatorial approach of next generation sequencing and de novo assembly to discover B. juncea transcriptome associated with high temperature and drought. Results: We constructed and sequenced three transcriptome libraries namely Brassica control (BC), Brassica high temperature stress (BHS) and Brassica drought stress (BDS) from control, high temperature treated and drought treated seedlings of Brassica juncea. More than 180 million purity filtered reads were generated which were processed through quality parameters and high quality reads were assembled de-novo using SOAPde-novo assembler. A total of 77750 unique transcripts were identified out of which 69,245 (89%) were annotated with high confidence. We established a subset of 19110 transcripts, which were differentially regulated by either high temperature and/or drought stress. Furthermore, 886 and 2834 transcripts that code for transcription factors and kinases, respectively, were also identified. Investigation of identified transcription factors revealed that 92 responded to high temperature, 72 exhibited alterations in expression during drought stress, and 60 were commonly associated with both the stresses. Similarly, 217, 259 and 193 kinases were responsive to high temperature, drought or both stresses, respectively. Maximum number of up-regulated transcription factors in high temperature and drought stress belonged to heat shock factors (HSFs) and dehydration responsive element-binding (DREB) families respectively. We also identified 239 metabolic pathways, which were perturbed during high temperature and drought treatments. Analysis of gene ontologies associated with differentially regulated genes forecasted their involvement in diverse biological processes. Conclusions: Our study provides first comprehensive discovery of B. juncea transcriptome under high temperature and drought stress conditions. Transcriptome resources generated in this study will enhance our understanding on the molecular mechanisms involved in defining the response of B. juncea against two important abiotic stresses. Furthermore this information would benefit designing of efficient crop improvement strategies for tolerance against conditions of high temperature regimes and water scarcity. Total three RNA-Seq libraries were prepared and sequenced independently [B. juncea control (BC), B. juncea high temperature stressed (BHS) and B. juncea drought stressed (BDS) on Illumina GAIIx sequencer].

Project description:Drought is an inevitable stress almost all terrestrial plants face in their life cycles. Desert dwelling plants show extreme adaptations to drought but their genomes are largely unexplored compared to drought sensitive model plants generally studied to understand plant drought tolerance. Haloxylon ammodendron is a pioneer species extremely tolerant to drought and capable of colonizing desert sand dunes. Seedling establishment is the most critical development stage in the survival of H. ammodendron. H. ammodendron seedlings are able to withstand high light, and low temperature stresses characteristic of temperate desert environments in addition to drought. We have investigated the genome-wide transcript responses under induced drought stress during early seedling establishment to identify prevailing basal and induced gene clusters that likely contribute to survival and stress adapted growth in H. ammodendron. We find staggering support for drought response transcript accumulation together with other transcripts that may transform the cellular expression space into a preadapted state for salt, light, osmotic, and temperature stress tolerance. While transcript accumulation is excessive for genes associated with abiotic stress tolerance under an induced drought treatment, H. ammodendron seems to enhance biotic stress tolerance simultaneously by down-regulation of several genes that would be found at an up-regulated state during pathogen entry in susceptible plants. We detected enriched basal level transcript allocation that suggests preadaptation to abiotic stresses as well as pathogen defense in H. ammodendron when compared to other Amaranthaceae family transcriptomes under stress neutral conditions. Amaranthaceae is one of the most enriched plant families for extremophytes. We found transcripts that are generally maintained at low levels and some induced only under abiotic stress in Arabidopsis thaliana to be highly expressed under basal conditions in the Amaranthaceae transcriptomes including H. ammodendron. These could be novel candidates to expand or initiate discovery of new stress adaptive gene networks and mechanisms naturally selected in extremophytes that allow survival under environmental stresses.

			Action	DRS
	SRR24487900_1.fastq.gz	Fastqsanger.gz
	SRR24487900_2.fastq.gz	Fastqsanger.gz
	SRR24487901_1.fastq.gz	Fastqsanger.gz
	SRR24487901_2.fastq.gz	Fastqsanger.gz
	SRR24487902_1.fastq.gz	Fastqsanger.gz

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