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首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >Sugarcane ESTs differentially expressed in immature and maturing internodal tissue
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Sugarcane ESTs differentially expressed in immature and maturing internodal tissue

机译:在未成熟和成熟的节间组织中差异表达的甘蔗EST

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Two subtracted cDNA libraries were constructed by reciprocal subtractive hybridisation between sugarcane immature (low sucrose-accumulating) and maturing (high sucrose-accumulating) internodal tissue. The subtracted libraries contained high, moderate and low abundance transcripts. To isolate cDNAs differentially expressed during culm maturation. 400 random clones (200 from each library) were systematically arrayed onto nylon filters and screened with total cDNA probes prepared from immature and maturing culm poly (A)(+) RNA. Results indicated that 36 and 30% of the total number of cDNAs analysed were preferentially expressed in the immature and maturing culm, respectively. Northern analysis of selected clones confirmed culm developmental stage-specific and -preferential expression for most of the clones tested. Expressed Sequence Tags (ESTs) generated by partial sequence analysis for all 132 differentially expressed clones indicated 95 unique transcripts. Partial sequence information could assign putative identities to 66% of the differentially expressed ESTs. The majority of ESTs with a putative identity were homologous to genes associated with cell wall metabolism. carbohydrate metabolism. stress responses and regulation, where the specific ESTs identified in the immature and maturing culm were distinct from each other. No developmentally regulated ESTs directly associated with sucrose metabolism were detected. This suggests that growth and maturation of the sugarcane culm is associated with the expression of genes for a variety of processes. This study demonstrates that a combination of cDNA subtraction with macroarray screening is an effective strategy to identify and analyse candidate developmentally regulated genes in sugarcane.
机译:通过在未成熟的甘蔗(积累低蔗糖)和成熟的(积累高蔗糖的)节间组织之间进行相互的减性杂交,构建了两个相减的cDNA文库。减去的文库包含高,中和低丰度转录物。分离在茎秆成熟过程中差异表达的cDNA。将400个随机克隆(每个文库200个)系统地排列在尼龙滤膜上,并用从未成熟和成熟的茎多(A)(+)RNA制备的总cDNA探针进行筛选。结果表明,分别在未成熟和成熟的茎中优先表达被分析的cDNA总数的36%和30%。所选克隆的Northern分析证实了大多数测试克隆的茎杆发育阶段特异性和优先表达。通过对全部132个差异表达克隆进行部分序列分析而生成的表达序列标签(EST),显示了95个独特的转录本。部分序列信息可以为66%的差异表达EST分配推定身份。多数具有假定身份的EST与与细胞壁代谢相关的基因同源。碳水化合物的代谢。压力反应和调节,其中在未成熟和成熟的茎中鉴定出的特定EST彼此不同。没有检测到与蔗糖代谢直接相关的受发育调节的EST。这表明甘蔗茎的生长和成熟与多种过程中基因的表达有关。这项研究表明,将cDNA减法与大阵列筛选相结合是鉴定和分析甘蔗中候选的发育调控基因的有效策略。

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