Panthee D R, Yuan J S, Wright D L, Marois J J, Mailhot D, Stewart C N
Department of Plant Sciences, University of Tennessee, Rm 252, Ellington Plant Sciences, 2431 Joe Johnson Dr., Knoxville, TN 37996, USA.
Funct Integr Genomics. 2007 Oct;7(4):291-301. doi: 10.1007/s10142-007-0045-8. Epub 2007 Feb 22.
Asian soybean rust (ASR) caused by Phakopsora pachyrhizi Sydow is a potentially devastating disease posing a serious threat to the soybean industry. Understanding plant host response at the molecular level is certainly important for control of the disease. The main objective of this study was to perform a transcriptome profiling of P. pachyrhizi-exposed young soybean plants (V2 growth stage) using whole genome Affymetrix microarrays of soybean. Three-week-old soybean cv. 5601 T plants at the V2 growth stage were inoculated with P. pachyrhizi, and leaf samples were collected 72 h post inoculation with subsequent microarray analysis performed. A total of 112 genes were found to be differentially expressed from P. pachyrhizi exposure, of which 46 were upregulated, and 66 were downregulated. Most of the differentially expressed genes were general defense and stress-related genes, and 34 of these were unknown. Confirmational real-time reverse transcription-polymerase chain reaction was performed on a subset of 5 out of 112 differentially expressed genes. These results were congruent with the microarray analysis. Our results indicated that low and nonspecific innate response to the pathogen may account for the failure to develop rust resistance in the soybean variety studied. To our knowledge, this is the first microarray analysis of soybean in response to ASR.
由大豆锈菌(Phakopsora pachyrhizi Sydow)引起的亚洲大豆锈病(ASR)是一种潜在的毁灭性病害,对大豆产业构成严重威胁。在分子水平上了解植物宿主的反应对于控制该病害无疑至关重要。本研究的主要目的是利用大豆全基因组Affymetrix微阵列对暴露于大豆锈菌的年轻大豆植株(V2生长阶段)进行转录组分析。将处于V2生长阶段的三周龄大豆品种5601 T植株接种大豆锈菌,接种后72小时采集叶片样本并进行后续的微阵列分析。共发现112个基因在暴露于大豆锈菌后差异表达,其中46个上调,66个下调。大多数差异表达基因是一般防御和胁迫相关基因,其中34个未知。对112个差异表达基因中的5个进行了验证性实时逆转录聚合酶链反应。这些结果与微阵列分析一致。我们的结果表明所研究的大豆品种对病原体的低水平和非特异性先天反应可能是其未能产生锈病抗性的原因。据我们所知,这是首次对大豆响应亚洲大豆锈病进行的微阵列分析。