首页> 美国卫生研究院文献>Plant Physiology >Expression of ADP-glucose pyrophosphorylase in maize (Zea mays L.) grain and source leaf during grain filling.
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Expression of ADP-glucose pyrophosphorylase in maize (Zea mays L.) grain and source leaf during grain filling.

机译:灌浆过程中ADP-葡萄糖焦磷酸化酶在玉米(Zea mays L.)籽粒和源叶中的表达。

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摘要

The time course of ADP-glucose pyrophosphorylase activity and of starch accumulation rate measured in grain, from pollination to maturity, in Zea mays L. plants grown outdoors, was coincident for 2 years. No such correlation was observed in the adjacent leaf, which, furthermore, presented large year-to-year differences in starch accumulation pattern. Analysis of the expression of ADP-glucose synthase at the protein levels, using antibodies directed against the Bt2 or Sh2 subunits, established that the variation of activity in the grain was explained by parallel changes in the content of both subunits. The cDNA for Bt2 and Sh2 subunits were used as probes to quantify the corresponding messenger. In grain, the time course of Bt2 and Sh2 mRNA accumulation anticipated, with a similar pattern, the specific peptide variations, which suggests a transcriptional control of expression. By contrast, the control of leaf activity by protein content was less obvious than in the grain, and changes in leaf enzyme specific activity were suggested during the first 20 d after pollination. A clone homologous to the grain Bt2 subunit cDNA was isolated from a maize leaf cDNA library, and a sequence comparison showed that the leaf clone (L2) was a partial cDNA representing one-third of the mature peptide. A 97% homology was observed between Bt2 and L2 in their coding region, but homology was poor in the 3' noncoding border. This result demonstrates that Bt2 and L2 arise from different genes presenting a tissue-specific expression pattern and provides an explanation for the earlier reported differences between leaf and grain in the size of peptide and mRNA for the Bt2-homologous subunit.
机译:在室外种植的玉蜀plants植物中,从授粉到成熟,谷物中ADP-葡萄糖焦磷酸化酶活性的时间过程和淀粉积累速率的时间一致,为两年。在相邻叶片中未观察到这种相关性,此外,淀粉积累模式的年际差异也很大。使用针对Bt2或Sh2亚基的抗体在蛋白质水平上分析ADP-葡萄糖合酶的表达,可以确定谷物中活性的变化可以通过两个亚基含量的平行变化来解释。 Bt2和Sh2亚基的cDNA被用作探针来量化相应的信使。在谷物中,Bt2和Sh2 mRNA积累的时间过程以相似的模式预测了特定的肽变异,这暗示了表达的转录控制。相比之下,通过蛋白质含量控制叶片活性的作用不如在谷物中明显,建议在授粉后20 d内改变叶片酶的比活性。从玉米叶片cDNA文库中分离出与谷物Bt2亚基cDNA同源的克隆,序列比较表明,叶片克隆(L2)是部分cDNA,代表了成熟肽的三分之一。在Bt2和L2的编码区域中观察到97%的同源性,但在3'非编码边界中同源性很差。该结果证明Bt2和L2来自呈现组织特异性表达模式的不同基因,并为较早报道的叶和谷之间在Bt2同源亚基的肽和mRNA的大小上的差异提供了解释。

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