Commonwealth Centre for Protein and Enzyme Technology, Bundoora, Victoria, 3083 Australia.
Plant Physiol. 1992 Jul;99(3):1226-31. doi: 10.1104/pp.99.3.1226.
Two genes encode (1-->3,1-->4)-beta-d-glucan 4-glucanohydrolase (EC 3.2.1.73) isoenzymes EI and EII in barley (Hordeum vulgare L.). Specific DNA probes have been used in Northern analyses to examine the developmental regulation of individual (1-->3,1-->4)-beta-glucanase genes in the aleurone and scutellum of germinated grain and in young leaves and young roots. In aleurone and scutella excised from germinated grain, mRNAs encoding both isoenzymes are present but developmental patterns differ between the two tissues. Thus, levels of both isoenzyme EI and EII mRNA increase significantly in the aleurone between 1 and 3 days after the initiation of germination. In the scutellum, isoenzyme EI mRNA predominates and decreases as germination proceeds. Isoenzyme EI mRNA appears in young leaves approximately 8 days after the initiation of germination and levels rise until about 20 days. Enzyme activity in leaf extracts parallels the development of isoenzyme EI mRNA. No isoenzyme EII mRNA is detected in the leaves in this period. Analysis of RNA from different leaf segments indicates that the isoenzyme EI mRNA is distributed relatively evenly along the length of the leaf. In young roots, mRNA encoding (1-->3,1-->4)-beta-glucanase isoenzyme EI is detected at high levels 3 to 6 days after the initiation of germination; again, little or no isoenzyme EII mRNA is found. Overall, transcription of the (1-->3,1-->4)-beta-glucanase isoenzyme EII gene appears to be restricted to the germinating grain, whereas isoenzyme EI is expressed in a wider range of tissues during seedling development.
两个基因编码(1-->3,1-->4)-β-d-葡聚糖 4-葡聚糖水解酶(EC 3.2.1.73)同工酶 EI 和 EII 在大麦(Hordeum vulgare L.)中。在Northern 分析中,已使用特定的 DNA 探针来研究萌发谷物的糊粉层和盾片中以及幼叶和幼根中单个(1-->3,1-->4)-β-葡聚糖酶基因的发育调控。在从萌发谷物中切除的糊粉层和盾片中,存在编码两种同工酶的 mRNA,但两种组织之间的发育模式不同。因此,在萌发开始后 1 至 3 天,两种同工酶 EI 和 EII 的 mRNA 水平均显著增加。在盾片中,同工酶 EI mRNA 占主导地位,并随着萌发的进行而减少。同工酶 EI mRNA 大约在萌发开始后 8 天出现在幼叶中,并且水平升高直到大约 20 天。叶片提取物中的酶活性与同工酶 EI mRNA 的发育相平行。在该时期,叶片中未检测到同工酶 EII mRNA。对来自不同叶片段的 RNA 的分析表明,同工酶 EI mRNA 沿叶片的长度相对均匀分布。在幼根中,在萌发开始后 3 至 6 天检测到编码(1-->3,1-->4)-β-葡聚糖酶同工酶 EI 的 mRNA 高水平;同样,发现很少或没有同工酶 EII mRNA。总体而言,(1-->3,1-->4)-β-葡聚糖酶同工酶 EII 基因的转录似乎仅限于萌发的谷物,而同工酶 EI 在幼苗发育过程中在更广泛的组织中表达。