Kaneko Yo-Hei, Inukai Tsuyoshi, Suehiro Noriko, Natsuaki Tomohide, Masuta Chikara
Graduate School of Agriculture, Hokkaido University, Sapporo 060-8589, Japan.
Theor Appl Genet. 2004 Dec;110(1):33-40. doi: 10.1007/s00122-004-1824-4. Epub 2004 Oct 29.
In the pathosystem of turnip mosaic virus (TuMV) and Arabidopsis thaliana, two distinct symptoms (mosaic symptom and veinal necrosis) were observed that were dependent upon the combination of the TuMV isolate and the Arabidopsis ecotype. The Col-0 ecotype developed mosaic symptoms after infection with the TuMV isolate Azu while the Ler ecotype developed veinal necrosis after infection with the same TuMV isolate. The Ler phenotype is controlled by a single dominant gene TuNI (TuMV necrosis inducer) which is located on chromosome 1. The TuNI gene was precisely mapped to the ~105 kb interval between the two markers of mXF41 and mRF28 by using several types of DNA polymorphism markers. Within this region, which included largely duplicated sequences, a total of 19 putative genes were predicted and 15 of these were classified into five gene families. The genes belonging to the gene families At1g58480 and At1g58602 may function in response to infection by pathogens. The gene family At1g58480 encodes lipase-like proteins, which might be involved in the induction of defence responses that are mediated by salicylic acid. The gene family At1g58602 encodes the CC-NBS-LRR (CNL) proteins, which are known to function as one of the plant resistance (R) proteins against pathogens. In the present study, the possibility that TuNI might function as an R gene was discussed.
在芜菁花叶病毒(TuMV)与拟南芥的病理系统中,观察到了两种不同的症状(花叶症状和叶脉坏死),这取决于TuMV分离株与拟南芥生态型的组合。Col-0生态型在被TuMV分离株Azu感染后出现花叶症状,而Ler生态型在被相同的TuMV分离株感染后出现叶脉坏死。Ler表型由位于1号染色体上的单个显性基因TuNI(TuMV坏死诱导因子)控制。通过使用几种类型的DNA多态性标记,TuNI基因被精确地定位到mXF41和mRF28这两个标记之间约105 kb的区间内。在这个主要包含重复序列的区域中,总共预测了19个推定基因,其中15个被归类为五个基因家族。属于基因家族At1g58480和At1g58602的基因可能在对病原体感染的反应中发挥作用。基因家族At1g58480编码类脂肪酶蛋白,其可能参与水杨酸介导的防御反应的诱导。基因家族At1g58602编码CC-NBS-LRR(CNL)蛋白,已知其作为植物抗病原体的抗性(R)蛋白之一发挥作用。在本研究中,讨论了TuNI可能作为R基因发挥作用 的可能性。