De Novo Assembly and Transcriptome Profiling of Ethiopian Lowland Bamboo Oxytenanthera Abyssinica (A. rich) Munro Under Drought and Salt Stresses

Muhamed Adem, Dereje Beyene, T. Feyissa, K. Zhao, T. Jiang
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Abstract

Bamboos are perennial grasses classified under family Poaceae and subfamily Bambusoideae and are among the fastest growing plants on earth. Despite ecological and economic significances, Ethiopian lowland bamboo (O. abyssinica) lacks global gene expression under abiotic stress. Plastic pot germinated seedlings of O. abyssinica were subjected to 200 µm NaCl and 25% PEG-6000 (Poly Ethylene glycol) to induce salt and drought stress, respectively. Using the Illumina sequencing platform, fifteen cDNA libraries were constructed and sequenced to generate the first drought and salt stress transcriptome profiling of the species so as to elucidate genome-wide transcriptome changes in response to such stresses. Following quality control, 754,444,646 clean paired-ends reads were generated, and then de novo assembled into 406,181 unigenes. Functional annotation against the public databases presented annotation of 217,067 (53.4%) unigenes, where NCBI-Nr 203,777, Swissport 115,741, COG 81,632 and KEGG 80,587. Prediction of Transcripts Factors (TFs) have generated 4,332 TFs organized into 64 TF families. Analysis of Differentially Expressed Genes (DEGs) provided 65,471 genes where 569 genes belong to all stresses. Protein families with a higher number of differentially expressed genes include bZIP (49), WRKY (43), MYB (38), AP2/ERF (30), HD-ZIP (25) and MYB related (21). In addition to revealing the genome-wide level appraisal of transcriptome resources of the species, this study also uncovered the comprehensive understanding of key stress responsive protein-coding genes, protein families and pathways which could be used as the basis for further studies.
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干旱和盐胁迫下埃塞俄比亚低地竹Oxytenanthera Abyssinica (A. rich) Munro的从头组装和转录组分析
竹是多年生禾本科植物,隶属于竹科和竹亚科,是地球上生长最快的植物之一。尽管具有生态和经济意义,埃塞俄比亚低地竹(O. abyssinica)在非生物胁迫下缺乏全球基因表达。用200µm NaCl和25% PEG-6000(聚乙二醇)分别处理深草塑料盆栽发芽苗,诱导盐胁迫和干旱胁迫。利用Illumina测序平台,构建了15个cDNA文库,并对其进行了测序,首次获得了该物种的干旱和盐胁迫转录组图谱,以阐明该物种在干旱和盐胁迫下的全基因组转录组变化。经过质量控制,生成了754,444,646个干净的对端reads,然后重新组装成406,181个unigenes。对公共数据库进行功能标注,共标注了217,067个(53.4%)unigenes,其中NCBI-Nr 203,777, Swissport 115,741, COG 81,632和KEGG 80,587。转录因子(TF)的预测已经产生了4332个TF,分为64个TF家族。差异表达基因(DEGs)分析得到65,471个基因,其中569个基因属于所有菌株。差异表达基因数量较多的蛋白家族包括bZIP(49)、WRKY(43)、MYB(38)、AP2/ERF(30)、HD-ZIP(25)和MYB相关(21)。本研究除了揭示了该物种转录组资源的全基因组水平评估外,还揭示了对关键应激反应蛋白编码基因、蛋白家族和途径的全面认识,可作为进一步研究的基础。
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