Pflanzenphysiologisches Institut der Universität, Altenbergrain 21, CH-3013, Bern, Switzerland.
Plant Mol Biol. 1989 Jun;12(6):643-54. doi: 10.1007/BF00044155.
Under normal growth conditions wheat shows 100% non-host resistance to the barley powdery mildew Erysiphe graminis f. sp. hordei (Egh.). Primary inoculation of 7-day-old wheat seedlings with this fungus induced partial (60-70%) local resistance to challenge inoculation 12 hours later with the compatible pathogen Erysiphe graminis f. sp. tritici (Egt). mRNA was isolated from induced resistant first leaves (13 hours after primary inoculation) and a cDNA library was established in lambda ZAP. Differential screening of the library with sDNA probes (from induced resistant versus non-inoculated plants) resulted in isolation of 6 cDNA clones corresponding to 6 different induced, plant-encoded mRNA species. Hybridization of in vitro transcripts derived from wheat nuclei to cDNA dot blots showed that the transcription of these genes was induced rapidly, 3 hours after inoculation with either Egt or Egh. At this time point neither fungus had formed appressorial germ tubes yet. When induced resistant first leaves were challenged with the compatible pathogen (Egt), transcription of the host genes was enhanced a second time. No difference in kinetics of induction of transcription could be observed between noninduced and induced resistant leaves. One of the cloned induced mRNAs codes for a peroxidase, as shown by cDNA derived partial peptide sequence analysis. Peroxidase activity increased in intercellular washing fluids of first leaves from 6 to 36 hours after inoculation.
在正常生长条件下,小麦对大麦白粉病菌(Egh.)表现出 100%的非寄主抗性。用这种真菌对 7 天大的小麦幼苗进行初次接种会诱导局部抗性(60-70%),12 小时后用相容病原体(Egt)进行挑战接种。从诱导抗性的第一片叶子(初次接种后 13 小时)中分离出 mRNA,并在 lambda ZAP 中建立 cDNA 文库。用 sDNA 探针(来自诱导抗性与未接种植物)对文库进行差异筛选,分离出 6 个 cDNA 克隆,对应 6 种不同的诱导、植物编码的 mRNA 种类。体外转录产物与 cDNA 点印迹杂交表明,这些基因的转录在接种 Egt 或 Egh 后 3 小时迅速诱导。此时,两种真菌都尚未形成附着胞芽管。当诱导抗性的第一片叶子受到相容病原体(Egt)的挑战时,宿主基因的转录再次增强。在非诱导和诱导抗性叶片之间,诱导转录的动力学没有差异。其中一个克隆的诱导 mRNA 编码一种过氧化物酶,如 cDNA 衍生的部分肽序列分析所示。接种后 6 至 36 小时,第一片叶子的细胞间洗涤液中的过氧化物酶活性增加。