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首页> 外文期刊>BMC Genomics >Microarray analysis and scale-free gene networks identify candidate regulators in drought-stressed roots of loblolly pine (P. taeda L.)
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Microarray analysis and scale-free gene networks identify candidate regulators in drought-stressed roots of loblolly pine (P. taeda L.)

机译:基因芯片分析和无标度基因网络可确定干旱胁迫下火炬松(P. taeda L.)的候选调控因子

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Background Global transcriptional analysis of loblolly pine (Pinus taeda L.) is challenging due to limited molecular tools. PtGen2, a 26,496 feature cDNA microarray, was fabricated and used to assess drought-induced gene expression in loblolly pine propagule roots. Statistical analysis of differential expression and weighted gene correlation network analysis were used to identify drought-responsive genes and further characterize the molecular basis of drought tolerance in loblolly pine. Results Microarrays were used to interrogate root cDNA populations obtained from 12 genotype × treatment combinations (four genotypes, three watering regimes). Comparison of drought-stressed roots with roots from the control treatment identified 2445 genes displaying at least a 1.5-fold expression difference (false discovery rate = 0.01). Genes commonly associated with drought response in pine and other plant species, as well as a number of abiotic and biotic stress-related genes, were up-regulated in drought-stressed roots. Only 76 genes were identified as differentially expressed in drought-recovered roots, indicating that the transcript population can return to the pre-drought state within 48 hours. Gene correlation analysis predicts a scale-free network topology and identifies eleven co-expression modules that ranged in size from 34 to 938 members. Network topological parameters identified a number of central nodes (hubs) including those with significant homology (E-values ≤ 2 × 10-30) to 9-cis-epoxycarotenoid dioxygenase, zeatin O-glucosyltransferase, and ABA-responsive protein. Identified hubs also include genes that have been associated previously with osmotic stress, phytohormones, enzymes that detoxify reactive oxygen species, and several genes of unknown function. Conclusion PtGen2 was used to evaluate transcriptome responses in loblolly pine and was leveraged to identify 2445 differentially expressed genes responding to severe drought stress in roots. Many of the genes identified are known to be up-regulated in response to osmotic stress in pine and other plant species and encode proteins involved in both signal transduction and stress tolerance. Gene expression levels returned to control values within a 48-hour recovery period in all but 76 transcripts. Correlation network analysis indicates a scale-free network topology for the pine root transcriptome and identifies central nodes that may serve as drivers of drought-responsive transcriptome dynamics in the roots of loblolly pine.
机译:背景技术由于有限的分子工具,对火炬松(Pinus taeda L.)的全球转录分析具有挑战性。 PtGen2,一个26,496个特征cDNA微阵列,被制造并用于评估干旱诱导的火炬松繁殖体根中的基因表达。利用差异表达的统计分析和加权基因相关网络分析来鉴定干旱响应基因,并进一步表征火炬松耐旱性的分子基础。结果微阵列被用于询问从12种基因型×处理组合(四种基因型,三种浇水方案)获得的根cDNA群体。将干旱胁迫的根与对照处理的根进行比较,鉴定出2445个基因表现出至少1.5倍的表达差异(假发现率= 0.01)。在干旱胁迫的根中,通常与松树和其他植物物种的干旱反应相关的基因以及许多与非生物和生物胁迫相关的基因被上调。在干旱恢复的根中只有76个基因被差异表达,这表明转录本种群可以在48小时内恢复到干旱前的状态。基因相关性分析可预测无标度的网络拓扑,并识别11个共表达模块,其大小范围从34到938个成员。网络拓扑参数确定了许多中心节点(集线器),包括与9-顺式-环氧类胡萝卜素双加氧酶,玉米素O-葡萄糖基转移酶和ABA具有显着同源性(E值≤2×10 -30 )的中心节点反应蛋白。识别出的集线器还包括以前与渗透压有关的基因,植物激素,使活性氧分子解毒的酶以及一些功能未知的基因。结论PtGen2被用于评估火炬松的转录组反应,并被用于鉴定根中严重干旱胁迫的2445个差异表达基因。已知许多鉴定出的基因响应于松树和其他植物物种中的渗透胁迫而被上调,并且编码参与信号转导和胁迫耐受性的蛋白质。除76个转录本外,所有基因转录水平在48小时的恢复期内均恢复到对照值。相关网络分析表明了松树根转录组的无标度网络拓扑,并确定了可以作为火炬松根部干旱响应转录组动力学驱动因素的中心节点。

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