Chaudhary Saurabh, Sharma Prakash C
University School of Biotechnology, Guru Gobind Singh Indraprastha University, New Delhi, 110078, India.
PLoS One. 2015 Mar 24;10(3):e0121982. doi: 10.1371/journal.pone.0121982. eCollection 2015.
Seabuckthorn (Hippophae rhamnoides L.), an important plant species of Indian Himalayas, is well known for its immense medicinal and nutritional value. The plant has the ability to sustain growth in harsh environments of extreme temperatures, drought and salinity. We employed DeepSAGE, a tag based approach, to identify differentially expressed genes under cold and freeze stress in seabuckthorn. In total 36.2 million raw tags including 13.9 million distinct tags were generated using Illumina sequencing platform for three leaf tissue libraries including control (CON), cold stress (CS) and freeze stress (FS). After discarding low quality tags, 35.5 million clean tags including 7 million distinct clean tags were obtained. In all, 11922 differentially expressed genes (DEGs) including 6539 up regulated and 5383 down regulated genes were identified in three comparative setups i.e. CON vs CS, CON vs FS and CS vs FS. Gene ontology and KEGG pathway analysis were performed to assign gene ontology term to DEGs and ascertain their biological functions. DEGs were mapped back to our existing seabuckthorn transcriptome assembly comprising of 88,297 putative unigenes leading to the identification of 428 cold and freeze stress responsive genes. Expression of randomly selected 22 DEGs was validated using qRT-PCR that further supported our DeepSAGE results. The present study provided a comprehensive view of global gene expression profile of seabuckthorn under cold and freeze stresses. The DeepSAGE data could also serve as a valuable resource for further functional genomics studies aiming selection of candidate genes for development of abiotic stress tolerant transgenic plants.
沙棘(Hippophae rhamnoides L.)是印度喜马拉雅地区的一种重要植物物种,以其巨大的药用和营养价值而闻名。该植物能够在极端温度、干旱和盐碱化等恶劣环境中维持生长。我们采用基于标签的方法DeepSAGE,来鉴定沙棘在寒冷和冻害胁迫下差异表达的基因。使用Illumina测序平台对包括对照(CON)、冷胁迫(CS)和冻害胁迫(FS)的三个叶片组织文库总共生成了3620万个原始标签,其中包括1390万个不同标签。在丢弃低质量标签后,获得了3550万个干净标签,其中包括700万个不同的干净标签。总共在三个比较组中,即CON与CS、CON与FS以及CS与FS中,鉴定出11922个差异表达基因(DEG),其中包括6539个上调基因和5383个下调基因。进行了基因本体论和KEGG通路分析,以将基因本体论术语分配给DEG并确定它们的生物学功能。将DEG映射回我们现有的由88297个假定单基因组成的沙棘转录组组装中,从而鉴定出428个对寒冷和冻害胁迫有响应的基因。使用qRT-PCR对随机选择的22个DEG的表达进行了验证,这进一步支持了我们的DeepSAGE结果。本研究提供了沙棘在寒冷和冻害胁迫下全球基因表达谱的全面视图。DeepSAGE数据也可以作为有价值的资源,用于进一步的功能基因组学研究,旨在选择候选基因以开发非生物胁迫耐受性转基因植物。