Vögeli-Lange R, Fründt C, Hart C M, Nagy F, Meins F
Friedrich Miescher-Institute, Basel, Switzerland.
Plant Mol Biol. 1994 May;25(2):299-311. doi: 10.1007/BF00023245.
The class I beta-1,3-glucanases are antifungal vacuolar proteins implicated in plant defense that show developmental, hormonal, and pathogenesis-related regulation. The tobacco enzymes are encoded by a small gene family with members derived from ancestors related to the present-day species Nicotiana sylvestris and N. tomentosiformis. We studied the expression in transgenic tobacco plants of a chimeric beta-glucuronidase (GUS) reporter gene fused to 1.6 kb of upstream sequence of the tobacco class I beta-1,3-glucanase B (GLB) gene, which is of N. tomentosiformis origin. Expression of the GUS reporter gene and the accumulation of class I beta-1,3-glucanase and its mRNA showed very similar patterns of regulation. In young seedlings the reporter gene was expressed in the roots. In mature tobacco plants it was preferentially expressed in lower leaves and roots and was induced in leaves by ethylene treatment and by infection with tobacco mosaic virus (TMV). Furthermore, it was down-regulated in cultured leaf discs by combinations of the hormones auxin and cytokinin. Histological studies of GUS activity showed that the GLB promoter shows highly localized expression in roots of seedlings. It is also expressed in a ring of cells around necrotic lesions induced by TMV infection, but not in cells immediately adjacent to the lesions or in the lesions themselves. The results of deletion analyses suggest that multiple positive and negative elements in the GLB promoter regulate its activity. The region from -1452 to -1193 containing two copies of the heptanucleotide AGCCGCC, which is highly conserved in plant-stress and defense-related genes, is necessary for high level expression in leaves. Additional regions important for organ-specific and regulated expression were: -568 to -402 for ethylene induction of leaves; -402 to -211 for expression in lower leaves and cultured leaf discs and for TMV induction of leaves; and -211 to -60 for expression in roots.
I类β-1,3-葡聚糖酶是参与植物防御的抗真菌液泡蛋白,表现出发育、激素和病程相关调控。烟草中的这些酶由一个小基因家族编码,其成员来源于与现今物种野生烟草和绒毛状烟草相关的祖先。我们研究了与烟草I类β-1,3-葡聚糖酶B(GLB)基因1.6 kb上游序列融合的嵌合β-葡萄糖醛酸酶(GUS)报告基因在转基因烟草植株中的表达,该GLB基因来源于绒毛状烟草。GUS报告基因的表达以及I类β-1,3-葡聚糖酶及其mRNA的积累显示出非常相似的调控模式。在幼苗中,报告基因在根中表达。在成熟烟草植株中,它优先在下部叶片和根中表达,并通过乙烯处理和烟草花叶病毒(TMV)感染在叶片中诱导表达。此外,在培养的叶盘中,生长素和细胞分裂素的组合会使其表达下调。对GUS活性的组织学研究表明,GLB启动子在幼苗根中表现出高度局部化的表达。它也在TMV感染诱导的坏死病斑周围的一圈细胞中表达,但不在紧邻病斑的细胞或病斑本身中表达。缺失分析的结果表明,GLB启动子中的多个正负调控元件调节其活性。从-1452到-1193的区域包含七核苷酸AGCCGCC的两个拷贝,该序列在植物应激和防御相关基因中高度保守,是叶片中高水平表达所必需的。对器官特异性和调控表达重要的其他区域包括:-568至-402用于叶片的乙烯诱导;-402至-211用于下部叶片和培养叶盘的表达以及叶片的TMV诱导;以及-211至-60用于根中的表达。