Hulzink Raymond J M, de Groot Peter F M, Croes Anton F, Quaedvlieg William, Twell Dave, Wullems George J, Van Herpen Marinus M A
Department of Experimental Botany, Plant Genetics, Catholic University Nijmegen, Toernooiveld 1, 6525 ED, Nijmegen, The Netherlands.
Plant Physiol. 2002 May;129(1):342-53. doi: 10.1104/pp.001701.
Transcripts of the ntp303 gene accumulate abundantly throughout pollen development, whereas the protein only accumulates to detectable levels after pollen germination. In an attempt to explain the divergence in the accumulation profiles of the mRNA and the protein, we investigated the role of the untranslated regions (UTRs) in enhancing ntp303 translation during the transition from developing to germinating pollen. Luciferase reporter gene fusion constructs containing the ntp303 5'-UTR gave rise to luciferase activity that was up to 60-fold higher during pollen tube growth than that of constructs containing different 5'-UTRs. No apparent differences in the luciferase activity of these constructs were observed during pollen development. The ntp303 5'-UTR-mediated increase in luciferase activity was not significantly influenced by coding region or 3'-UTR sequences. Furthermore, enhanced luciferase activity directed by the ntp303 5'-UTR occurred predominantly at the post-transcriptional level. A series of 5'-UTR deletion constructs was created to identify putative regulatory sequences required for the high level of translation during pollen tube growth. Two predicted stem loop structures (H-I and H-II) caused a complete inhibition of the enhanced translation after their total or partial deletion. A (GAA)(8) repeat within the H-I stem loop structure was demonstrated to be important for the modulation of translation efficiency. The H-II stem loop structure was found to be essential for the determination of mRNA stability.
ntp303基因的转录本在整个花粉发育过程中大量积累,而该蛋白仅在花粉萌发后才积累到可检测水平。为了解释mRNA和蛋白质积累模式的差异,我们研究了非翻译区(UTR)在花粉从发育到萌发的转变过程中增强ntp303翻译的作用。含有ntp303 5'-UTR的荧光素酶报告基因融合构建体在花粉管生长期间产生的荧光素酶活性比含有不同5'-UTR的构建体高60倍。在花粉发育过程中,未观察到这些构建体的荧光素酶活性有明显差异。ntp303 5'-UTR介导的荧光素酶活性增加不受编码区或3'-UTR序列的显著影响。此外,ntp303 5'-UTR指导的荧光素酶活性增强主要发生在转录后水平。构建了一系列5'-UTR缺失构建体,以鉴定花粉管生长期间高水平翻译所需的假定调控序列。两个预测的茎环结构(H-I和H-II)在完全或部分缺失后导致增强翻译的完全抑制。H-I茎环结构内的一个(GAA)(8)重复序列被证明对翻译效率的调节很重要。发现H-II茎环结构对于mRNA稳定性的确定至关重要。