Deguchi Yuichi, Banba Mari, Shimoda Yoshikazu, Chechetka Svetlana A, Suzuri Ryota, Okusako Yasuhiro, Ooki Yasuhiro, Toyokura Koichi, Suzuki Akihiro, Uchiumi Toshiki, Higashi Shiro, Abe Mikiko, Kouchi Hiroshi, Izui Katsura, Hata Shingo
Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
DNA Res. 2007 Jun 30;14(3):117-33. doi: 10.1093/dnares/dsm014.
To better understand the molecular responses of plants to arbuscular mycorrhizal (AM) fungi, we analyzed the differential gene expression patterns of Lotus japonicus, a model legume, with the aid of a large-scale cDNA macroarray. Experiments were carried out considering the effects of contaminating microorganisms in the soil inoculants. When the colonization by AM fungi, i.e. Glomus mosseae and Gigaspora margarita, was well established, four cysteine protease genes were induced. In situ hybridization revealed that these cysteine protease genes were specifically expressed in arbuscule-containing inner cortical cells of AM roots. On the other hand, phenylpropanoid biosynthesis-related genes for phenylalanine ammonia-lyase (PAL), chalcone synthase, etc. were repressed in the later stage, although they were moderately up-regulated on the initial association with the AM fungus. Real-time RT-PCR experiments supported the array experiments. To further confirm the characteristic expression, a PAL promoter was fused with a reporter gene and introduced into L. japonicus, and then the transformants were grown with a commercial inoculum of G. mosseae. The reporter activity was augmented throughout the roots due to the presence of contaminating microorganisms in the inoculum. Interestingly, G. mosseae only colonized where the reporter activity was low. Comparison of the transcriptome profiles of AM roots and nitrogen-fixing root nodules formed with Mesorhizobium loti indicated that the PAL genes and other phenylpropanoid biosynthesis-related genes were similarly repressed in the two organs.
为了更好地理解植物对丛枝菌根(AM)真菌的分子响应,我们借助大规模cDNA宏阵列分析了模式豆科植物百脉根的差异基因表达模式。实验考虑了土壤接种剂中污染微生物的影响。当AM真菌(即摩西球囊霉和珠状巨孢囊霉)的定殖良好建立时,四个半胱氨酸蛋白酶基因被诱导。原位杂交显示这些半胱氨酸蛋白酶基因在AM根含丛枝的内皮层细胞中特异性表达。另一方面,苯丙氨酸解氨酶(PAL)、查尔酮合酶等苯丙烷生物合成相关基因在后期被抑制,尽管它们在与AM真菌最初关联时适度上调。实时RT-PCR实验支持了阵列实验。为了进一步证实特征性表达,将一个PAL启动子与一个报告基因融合并导入百脉根,然后用摩西球囊霉的商业接种剂培养转化体。由于接种剂中存在污染微生物,整个根系的报告基因活性增强。有趣的是,摩西球囊霉仅在报告基因活性低的地方定殖。对AM根和与中慢生根瘤菌形成的固氮根瘤的转录组图谱比较表明,PAL基因和其他苯丙烷生物合成相关基因在这两个器官中同样被抑制。