Department of Plant Science, University of Manitoba, 222 Agriculture Building, Winnipeg R3T2N2, Canada.
J Integr Plant Biol. 2010 May;52(5):453-67. doi: 10.1111/j.1744-7909.2010.00943.x.
Using a subtractive hybridization (SH)/cDNA-AFLP combinational approach, differentially expressed genes involved in the potato-Phytophthora infestans interaction were identified. These included genes potentially controlling pathogenesis or avr genes in P. infestans as well as those potentially involved in potato resistance or susceptibility to this pathogen. Forty-one differentially expressed transcript-derived fragments (TDFs), resulting from the interaction, were cloned and sequenced. Two TDFs, suggested as potential pathogenicity factors, have sequence similarity to N-succinyl diaminopimelate aminotransferase and a transcriptional regulator, TetR family gene, respectively. Two other TDFs, suggested as potential avr genes, have sequence similarity to an EST sequence from Avr4/Cf-4/Avr9/Cf-9 and a P. infestans avirulence-associated gene, respectively. Genes' expression and origin were confirmed using Southern blots, Northern blots and qRT-PCR. I.e., potential resistance gene DL81 was induced at 12 hpi in the moderately resistant cultivar, whereas it was down-regulated as early as 6 hpi in the susceptible cultivar. On the other hand, DL21 was induced at 6 hpi (3.38-fold) in response to the highly aggressive isolate (US8) and strongly up-regulated thereafter (25.13-fold at 120 hpi.), whereas it was only slightly up-regulated in response to the weakly aggressive isolate US11 (3.82-fold at 96 hpi), suggesting its potential involvement as a susceptibility gene.
利用消减杂交(SH)/cDNA-AFLP 组合方法,鉴定了参与马铃薯-致病疫霉互作的差异表达基因。这些基因包括可能控制致病疫霉的致病性或 avr 基因的基因,以及可能参与马铃薯对该病原体的抗性或敏感性的基因。从互作中克隆和测序了 41 个差异表达的转录衍生片段(TDFs)。两个 TDFs 分别与 N-琥珀酰二氨基庚二酸氨基转移酶和 TetR 家族基因的转录调节剂具有序列相似性,被认为是潜在的致病性因素。另外两个 TDFs 与来自 Avr4/Cf-4/Avr9/Cf-9 的 EST 序列和致病疫霉无毒相关基因具有序列相似性,被认为是潜在的 avr 基因。使用 Southern 印迹、Northern 印迹和 qRT-PCR 证实了基因的表达和来源。即,中度抗性品种中的潜在抗性基因 DL81 在 12 hpi 时被诱导,而在易感品种中早在 6 hpi 时就被下调。另一方面,DL21 在响应高度侵袭性分离株(US8)时在 6 hpi 时被诱导(3.38 倍),此后强烈上调(120 hpi 时上调 25.13 倍),而在响应弱侵袭性分离株 US11 时仅轻度上调(96 hpi 时上调 3.82 倍),表明其可能作为敏感性基因参与。