首页> 外文期刊>Planta: An International Journal of Plant Biology >Identification of expression profiles of tapping panel dryness (TPD) associated genes from the latex of rubber tree (Hevea brasiliensis Muell. Arg.)
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Identification of expression profiles of tapping panel dryness (TPD) associated genes from the latex of rubber tree (Hevea brasiliensis Muell. Arg.)

机译:从橡胶树的乳胶(Hevea brasiliensis Muell。Arg。)的出胶板干燥(TPD)相关基因的表达谱的鉴定。

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Tapping panel dryness (TPD) occurrence in high latex yielding rubber tree (Hevea brasiliensis) is characterized by the partial or complete cessation of latex flow upon tapping leading to severe loss in natural rubber production around the world. The goal of this study was to identify genes whose mRNA transcript levels are differentially regulated in rubber tree during the onset of TPD. To isolate TPD responsive genes, two cDNA libraries (forward and reverse) from total RNA isolated from latex of healthy and TPD trees were constructed using suppression subtractive hybridization (SSH) method. In total, 1,079 EST clones were obtained from two cDNA libraries and screened by reverse Northern blot analysis. Screening results revealed that about 352 clones were differentially regulated and they were selected for sequencing. Based on the nucleotide sequence data, the putative functions of cDNA clones were predicted by BLASTX/BLASTN analysis. Among these, 64 were genes whose function had been previously identified while the remaining clones were genes with either unknown protein function or insignificant similarity to other protein/DNA/EST sequences in existing databases. RT-PCR analysis was carried out to validate the up-regulated genes from both the libraries. Among them, two genes were strongly down-regulated in TPD trees. The level of mRNA transcripts of these two genes was further examined by conventional Northern and RT-PCR analysis. Results indicated that the expression level of two genes was significantly lower in TPD trees compared to healthy trees. Many TPD associated genes were also up-regulated in TPD trees suggesting that they may be involved in triggering programmed cell death (PCD) during the onset of TPD syndrome. The results presented here demonstrate that SSH technique provides a powerful complementary approach for the identification of TPD related genes from rubber tree.
机译:高产胶乳橡胶树(巴西橡胶树)的丝板干燥(TPD)发生的特征是,出胶时胶乳流动部分或完全停止,导致全世界天然橡胶生产的严重损失。这项研究的目的是鉴定在TPD发病期间橡胶树中mRNA转录水平受到差异调节的基因。为了分离TPD响应基因,使用抑制消减杂交(SSH)方法从健康和TPD树的乳胶中分离的总RNA中构建了两个cDNA文库(正向和反向)。从两个cDNA文库中总共获得了1,079个EST克隆,并通过反向Northern印迹分析进行了筛选。筛选结果表明,约有352个克隆受到差异调节,并选择它们进行测序。基于核苷酸序列数据,通过BLASTX / BLASTN分析预测了cDNA克隆的假定功能。在这些基因中,有64个基因的功能先前已被鉴定,而其余的克隆是具有未知蛋白质功能或与现有数据库中其他蛋白质/ DNA / EST序列相似性不显着的基因。进行RT-PCR分析以验证来自两个文库的上调基因。其中,两个基因在TPD树中被强烈下调。通过常规Northern和RT-PCR分析进一步检查了这两个基因的mRNA转录物水平。结果表明,与健康树相比,TPD树中两个基因的表达水平显着降低。 TPD树中许多与TPD相关的基因也上调,表明它们可能与TPD综合征发作期间触发程序性细胞死亡(PCD)有关。此处显示的结果表明SSH技术为从橡胶树中鉴定TPD相关基因提供了强大的补充方法。

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