Lu J L, Ertl J R, Chen C M
Department of Biological Sciences, University of Wisconsin-Parkside, Kenosha 53141.
Plant Mol Biol. 1990 Apr;14(4):585-94. doi: 10.1007/BF00027504.
To investigate the molecular mechanism of cytokinin regulation of nitrate reductase (NR) activity, the influence of benzyladenine (BA) on the level of NR transcript was studied in etiolated barley leaves using a barley NR cDNA as a probe. Northern blot analyses of the levels of NR poly (A)+ RNA indicate that the amount present is proportional to the concentration of BA (2 x 10(-8) to 2 x 10(-4) M) applied to the leaves. Enhancement of NR mRNA by 2 x 10(-5) M BA was clearly detected after 15 minutes of exposure of the leaves to light. The enhancement is cytokinin-specific and adenine is ineffective. Brief treatment with the protein synthesis inhibitor, cycloheximide, inhibited BA-enhanced NR activity but did not inhibit BA-enhanced NR transcript level, thus the enhancement was independent of concurrent protein synthesis. Nuclear runoff transcription studies showed that the enhancement of NR mRNA was at least partially due to increased transcription rates.
为了研究细胞分裂素调节硝酸还原酶(NR)活性的分子机制,以大麦NR cDNA为探针,研究了苄基腺嘌呤(BA)对黄化大麦叶片中NR转录水平的影响。对NR多聚腺苷酸(poly (A)+)RNA水平的Northern印迹分析表明,其含量与施加到叶片上的BA浓度(2×10⁻⁸至2×10⁻⁴M)成正比。在叶片光照15分钟后,明显检测到2×10⁻⁵M BA增强了NR mRNA。这种增强是细胞分裂素特异性的,腺嘌呤无效。用蛋白质合成抑制剂环己酰亚胺短暂处理,抑制了BA增强的NR活性,但没有抑制BA增强的NR转录水平,因此这种增强与同时进行的蛋白质合成无关。核转录延伸实验表明,NR mRNA的增强至少部分是由于转录速率增加。