Jiang Qian-Tao, Liu Tao, Ma Jian, Wei Yu-Ming, Lu Zhen-Xiang, Lan Xiu-Jin, Dai Shou-Fen, Zheng You-Liang
Triticeae Research Institute, Sichuan Agricultural University, Chengdu 611130, Sichuan, China.
Genetica. 2011 Oct;139(10):1283-92. doi: 10.1007/s10709-012-9630-4.
The pre-mRNA processing (Prp1) gene encodes a spliceosomal protein. It was firstly identified in fission yeast and plays a regular role during spliceosome activation and cell cycle. Plant Prp1 genes have only been identified from rice, Sorghum and Arabidopsis thaliana. In this study, we reported the identification and isolation of a novel Prp1 gene from barley, and further explored its expressional pattern by using real-time quantitative RTPCR, promoter prediction and analysis of microarray data. The putative barley Prp1 protein has a similar primary structure features to those of other known Prp1 protein in this family. The results of amino acid comparison indicated that Prp1 protein of barley and other plant species has a highly conserved 30 termnal region while their 50 sequences greatly varied. The results of expressional analysis revealed that the expression level of barley Prp1 gene is always stable in different vegetative tissues, except it is up-regulated at the mid- and late stages of seed development or under the condition of cold stress. This kind of expressional pattern for barley Prp1 is also supported by our results of comparison of microarray data from barley, rice and Arabidopsis. For the molecular mechanism of its expressional pattern, we conclude that the expression of Prp1 gene may be up-regulated by the increase of pre-mRNAs and not be constitutive or ubiquitous.
前体mRNA加工(Prp1)基因编码一种剪接体蛋白。它最初在裂殖酵母中被鉴定出来,在剪接体激活和细胞周期中发挥常规作用。植物Prp1基因仅在水稻、高粱和拟南芥中被鉴定出来。在本研究中,我们报道了从大麦中鉴定和分离出一个新的Prp1基因,并通过实时定量RT-PCR、启动子预测和微阵列数据分析进一步探索了其表达模式。推测的大麦Prp1蛋白与该家族中其他已知的Prp1蛋白具有相似的一级结构特征。氨基酸比较结果表明,大麦和其他植物物种的Prp1蛋白在30端区域具有高度保守性,而其50序列差异很大。表达分析结果显示,大麦Prp1基因在不同营养组织中的表达水平始终稳定,除了在种子发育的中后期或冷胁迫条件下上调。我们对大麦、水稻和拟南芥微阵列数据的比较结果也支持了大麦Prp1的这种表达模式。对于其表达模式的分子机制,我们得出结论,Prp1基因的表达可能因前体mRNA的增加而上调,并非组成型或普遍存在。