Anand Ajith, Schmelz Eric A, Muthukrishnan Subbaratnam
Department of Biochemistry, Kansas State University, Manhattan, KS 66506, USA.
Mol Plant Microbe Interact. 2003 Oct;16(10):916-25. doi: 10.1094/MPMI.2003.16.10.916.
In the course of coexpressing genes for pathogenesis-related (PR) proteins for a class IV chitinase and an acidic glucanase in transgenic wheat plants, we regenerated a wheat line that developed necrotic lesions containing dead cells in the T2 and subsequent generations. Lesion spots were detected at the booting stage (5- to 6-week-old plants) in lines homozygous for the transgene loci. In contrast, lesions were not observed in hemizygous transgenic lines or lines silenced for transgene expression, indicating a requirement for high levels of transgene expression for the development of the lesioned phenotype. Lesion development was associated with the accumulation of host-encoded PR proteins, e.g., chitinases, beta-1,3-glucanases, thaumatin-like protein, and production of reactive oxygen intermediates. F1 progeny of a cross between the lesion-plus transgenic line and wild-type nontransgenic plants produced progeny with a normal phenotype, while the F2 progenies segregated for the lesion phenotype. Salicylic acid (SA) levels in plants with the lesion-plus phenotype were found to be several times higher than controls and nearly double the levels in hemizygous transgenic plants that lack lesions. SA application activated lesion development in excised leaf pieces of these hemizygous transgenic plants. Similar activation of lesion development in control plants occurred only when high concentrations of SA were applied for prolonged periods. Transcripts for phenylalanine-ammonia lyase, which provides precursors of SA, were elevated in homozygous transgenic plants. Our data suggest that transgene-induced lesion-mimic phenotype correlates with enhanced SA biosynthesis.
在转基因小麦植株中共表达病程相关(PR)蛋白(IV类几丁质酶和酸性葡聚糖酶)基因的过程中,我们培育出了一个小麦株系,该株系在T2代及后续世代中出现了含有死细胞的坏死病斑。在转基因位点纯合的株系中,孕穗期(5至6周龄植株)就能检测到病斑。相比之下,在半合子转基因株系或转基因表达沉默的株系中未观察到病斑,这表明病斑表型的出现需要高水平的转基因表达。病斑的发展与宿主编码的PR蛋白(如几丁质酶、β-1,3-葡聚糖酶、类甜蛋白)的积累以及活性氧中间体的产生有关。病斑阳性转基因株系与野生型非转基因植株杂交产生的F1代子代具有正常表型,而F2代子代出现病斑表型分离。发现有病斑阳性表型的植株中水杨酸(SA)水平比对照高出几倍,几乎是无病斑的半合子转基因植株中SA水平的两倍。SA处理激活了这些半合子转基因植株离体叶片的病斑发展。只有在长时间施加高浓度SA时,对照植株才会出现类似的病斑发展激活现象。为SA提供前体的苯丙氨酸解氨酶的转录本在纯合转基因植株中升高。我们的数据表明,转基因诱导的类病斑表型与SA生物合成增强相关。