Department of Plant Science, School of Agriculture and Biology, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, People's Republic of China.
Mol Biol Rep. 2013 Apr;40(4):2915-26. doi: 10.1007/s11033-012-2307-3. Epub 2012 Dec 1.
In order to better understand the mechanisms by which muskmelons (Cucumis melo L.) respond to salt stress, a cDNA library was constructed using suppression subtractive hybridization (SSH) from the root tissue of a salt-tolerant melon cultivar, Bingxuecui. A total of 339 clones were sequenced from the SSH library, leading to 312 high quality expressed sequence tags (ESTs), with an average size of 450 bp; representing 262 uni-ESTs comprising 29 contigs and 233 singletons. Blast analysis of the deduced protein sequences revealed that 283 ESTs had a high similarity to proteins in the non-redundant database, while 29 had low identity or no similarities. Many of the annotated sequences were homologous to genes involved in abiotic or biotic stress in plants. Functional categorization of the proteins revealed that salt tolerance could be largely determined by various proteins involved in metabolism, energy, transcription, signal transduction, protein fate, cell rescue and defense, implying a complex response to salt stress exists in melon plants. Twenty-seven ESTs were selected and analyzed by real-time PCR; the results confirmed that a high proportion of the ESTs were activated by salt stress. The complete sequences and a detailed functional analysis of these ESTs is required, in order to fully understand the broader impact of these genes in plants subjected to a high salinity environment.
为了更好地理解厚皮甜瓜(Cucumis melo L.)响应盐胁迫的机制,我们利用耐盐甜瓜品种‘冰雪脆’的根组织进行抑制性消减杂交(SSH)构建了 cDNA 文库。从 SSH 文库中测序得到了 339 个克隆,得到了 312 个高质量的表达序列标签(ESTs),平均大小为 450bp;代表 262 个单 ESTs,包括 29 个 contigs 和 233 个 singletons。推测的蛋白质序列的 Blast 分析表明,283 个 ESTs 与非冗余数据库中的蛋白质具有高度相似性,而 29 个 ESTs 具有低同一性或无相似性。许多注释的序列与植物中涉及非生物或生物胁迫的基因同源。蛋白质的功能分类表明,盐耐受性可能主要由参与代谢、能量、转录、信号转导、蛋白质命运、细胞拯救和防御的各种蛋白质决定,这表明甜瓜植物对盐胁迫存在复杂的反应。选择了 27 个 ESTs 并通过实时 PCR 进行了分析;结果证实,高比例的 ESTs 被盐胁迫激活。为了充分了解这些基因在高盐环境下对植物的更广泛影响,需要对这些 ESTs 的完整序列和详细功能进行分析。