Ohme-Takagi M, Shinshi H
Laboratory of Plant Molecular Biology, Fermentation Research Institute, Ibaraki, Japan.
Plant Mol Biol. 1990 Dec;15(6):941-6. doi: 10.1007/BF00039434.
We determined the primary structure of a tobacco beta-1,3-glucanase gene. The beta-1,3-glucanase gene has a single large intron, and the intron separates coding regions of the signal peptide and the mature enzyme. Analysis of the 5'-flanking region sequence revealed an 11 bp GC-rich element with perfect homology to the putative regulatory sequence of tobacco chitinase genes. RNA blot analysis showed that levels of mRNAs of beta-1,3-glucanase and chitinase are coordinately increased in response to ethylene and salicylic acid. Accumulation of beta-1,3-glucanase mRNA in suspension-cultured cells is rapidly induced at late logarithmic growth phase. Members of the tobacco beta-1,3-glucanase gene families are classified into two subfamilies. One of the subfamilies appeared to be transcriptionally inactive.
我们确定了烟草β-1,3-葡聚糖酶基因的一级结构。该β-1,3-葡聚糖酶基因有一个大的内含子,此内含子将信号肽和成熟酶的编码区域分隔开。对5'-侧翼区序列的分析揭示了一个11bp富含GC的元件,它与烟草几丁质酶基因的假定调控序列具有完全同源性。RNA印迹分析表明,β-1,3-葡聚糖酶和几丁质酶的mRNA水平在乙烯和水杨酸的作用下协同增加。悬浮培养细胞中β-1,3-葡聚糖酶mRNA的积累在对数生长后期被迅速诱导。烟草β-1,3-葡聚糖酶基因家族的成员被分为两个亚家族。其中一个亚家族似乎是转录无活性的。