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Timecourse microarray analyses reveal global changes in gene expression of susceptible Glycine max (soybean) roots during infection by Heterodera glycines (soybean cyst nematode)

机译:时程微阵列分析揭示了异型甘氨酸(大豆孢囊线虫)感染过程中易感大豆最大(大豆)根基因表达的总体变化

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Changes in gene expression within roots of Glycine max (soybean), cv. Kent, susceptible to infection by Heterodera glycines (the soybean cyst nematode [SCN]), at 6, 12, and 24 h, and 2, 4, 6, and 8 days post-inoculation were monitored using microarrays containing more than 6,000 cDNA inserts. Replicate, independent biological samples were examined at each time point. Gene expression was analyzed statistically using T-tests, ANOVA, clustering algorithms, and online analytical processing (OLAP). These analyses allow the user to query the data in several ways without importing the data into third-party software. RT-PCR confirmed that WRKY6 transcription factor, trehalose phosphate synthase, EIF4a, Skp1, and CLB1 were differentially induced across most time-points. Other genes induced across most timepoints included lipoxygenase, calmodulin, phospholipase C, metallothionein-like protein, and chalcone reductase. RT-PCR demonstrated enhanced expression during the first 12 h of infection for Kunitz trypsin inhibitor and sucrose synthase. The stress-related gene, SAM-22, phospholipase D and 12-oxophytodienoate reductase were also induced at the early time-points. At 6 and 8 dpi there was an abundance of transcripts expressed that encoded genes involved in transcription and protein synthesis. Some of those genes included ribosomal proteins, and initiation and elongation factors. Several genes involved in carbon metabolism and transport were also more abundant. Those genes included glyceraldehyde 3-phosphate dehydrogenase, fructose-bisphosphate aldolase and sucrose synthase. These results identified specific changes in gene transcript levels triggered by infection of susceptible soybean roots by SCN.
机译:Glycine max(大豆)根内基因表达的变化。使用含有6,000多个cDNA插入片段的微阵列,在接种后6、12和24小时以及2、4、6和8天监测肯特氏菌(Kent)易受Heterodera甘氨酸(大豆孢囊线虫[SCN])感染。在每个时间点检查复制的独立生物样品。使用T检验,ANOVA,聚类算法和在线分析处理(OLAP)对基因表达进行统计分析。这些分析允许用户以多种方式查询数据,而无需将数据导入第三方软件。逆转录-聚合酶链反应证实WRKY6转录因子,海藻糖磷酸合酶,EIF4a,Skp1和CLB1在大多数时间点被诱导分化。在大多数时间点诱导的其他基因包括脂氧合酶,钙调蛋白,磷脂酶C,类金属硫蛋白和查尔酮还原酶。 RT-PCR证明Kunitz胰蛋白酶抑制剂和蔗糖合酶在感染的前12 h表达增强。在早期时间点也诱导了与压力有关的基因SAM-22,磷脂酶D和12-氧代乙二酸酯还原酶。在6和8 dpi时,有大量的转录物表达出来,这些转录物编码参与转录和蛋白质合成的基因。这些基因中的一些包括核糖体蛋白,起始和延伸因子。参与碳代谢和运输的几个基因也更加丰富。这些基因包括甘油醛3-磷酸脱氢酶,果糖-双磷酸醛缩酶和蔗糖合酶。这些结果确定了由SCN感染易感大豆根引发的基因转录水平的特定变化。

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