Yamamoto-Katou Ayako, Katou Shinpei, Yoshioka Hirofumi, Doke Noriyuki, Kawakita Kazuhito
Plant Pathology Laboratory, Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa-ku, Nagoya, 464-8601 Japan.
Plant Cell Physiol. 2006 Jun;47(6):726-35. doi: 10.1093/pcp/pcj044. Epub 2006 Apr 11.
Recent works have established a key role for nitric oxide (NO) in activating disease resistance in plants. Nitrate reductase (NR) is one of the enzymes that are capable of producing NO in plants. In a previous study, we reported that pathogen signals induce expression of NR genes in potato, suggesting the involvement of NR in NO production induced by pathogen signals. In this study, we cloned NR genes from Nicotiana benthamiana and investigated their involvement in NO production induced by INF1, a major elicitin secreted by Phytophthora infestans. Treatment of protoplasts prepared from N. benthamiana leaves with INF1 elevated NO production to a maximum level 1-3 h after treatment. INF1-induced NO generation was suppressed completely by an NO-specific scavenger, but partially by a nitric oxide synthase inhibitor. To investigate the involvement of NR in INF1-induced NO production, NR genes were silenced by virus-induced gene silencing. The NR-silenced plants showed yellowish leaves which resemble the characteristic of Arabidopsis NR double mutants. Silencing of NR genes significantly decreased both NO(2) (-)-producing activity and INF1-induced NO production, indicating that NR is involved in INF1-induced NO production. In contrast, overexpression of NbNR1 encoding N. benthamiana NR by Agrobacterium-mediated transient expression elevated NO(2) (-)-producing activity nine times over the control; however, INF1-induced NO production in protoplasts overexpressing NbNR1 was comparable with that in control protoplasts. These results suggest that NR is involved in INF1-induced NO production, and post-translational modification of NR or availability of substrate NO(2) (-) may be a rate-limiting step of NO production by NR.
近期研究表明,一氧化氮(NO)在激活植物抗病性方面发挥着关键作用。硝酸还原酶(NR)是植物中能够产生NO的酶之一。在之前的一项研究中,我们报道病原体信号可诱导马铃薯中NR基因的表达,这表明NR参与了病原体信号诱导的NO产生过程。在本研究中,我们从本氏烟草中克隆了NR基因,并研究了它们在由致病疫霉分泌的主要激发子INF1诱导的NO产生过程中的作用。用INF1处理本氏烟草叶片制备的原生质体后,NO产量在处理后1 - 3小时达到最高水平。INF1诱导的NO生成被NO特异性清除剂完全抑制,但被一氧化氮合酶抑制剂部分抑制。为了研究NR在INF1诱导的NO产生中的作用,通过病毒诱导的基因沉默使NR基因沉默。NR基因沉默的植株叶片发黄,类似于拟南芥NR双突变体的特征。NR基因的沉默显著降低了NO₂⁻产生活性以及INF1诱导的NO产生,表明NR参与了INF1诱导的NO产生。相比之下,通过农杆菌介导的瞬时表达过表达编码本氏烟草NR的NbNR1,使NO₂⁻产生活性比对照提高了九倍;然而,在过表达NbNR1的原生质体中,INF1诱导的NO产生与对照原生质体相当。这些结果表明,NR参与了INF1诱导的NO产生,并且NR的翻译后修饰或底物NO₂⁻的可用性可能是NR产生NO的限速步骤。