Li Qian-Feng, Zhang Gui-Yun, Dong Zhi-Wei, Yu Heng-Xiu, Gu Ming-Hong, Sun Samuel S M, Liu Qiao-Quan
Yangzhou University, Jiangsu, China.
Plant Physiol Biochem. 2009 May;47(5):351-8. doi: 10.1016/j.plaphy.2009.02.001. Epub 2009 Feb 12.
Starch-debranching enzymes (DBEs) are key enzymes involved in starch metabolism in cereals, having a dual function, in both starch synthesis and degradation. However, their precise roles in this pathway, particularly their expression profiles, remain unclear. In the present study, we performed a quantitative real-time PCR (Q-PCR) analysis of the expression pattern of the OsPUL gene encoding a pullulanase-type DBE in different tissues as well as in seeds at different developmental stages. The results showed that this gene was expressed only in seeds. In addition, the 1177-bp OsPUL promoter sequence was cloned, and some endosperm-specific motifs such as the GCN4 and AACA motifs were observed to exist in this region. The promoter was then fused with the GUS reporter gene and its expression was carefully investigated in transgenic rice. The data from both histochemical and fluorometric analyses showed that the OsPUL promoter was capable of driving the target gene to have a high level of endosperm-specific expression. The OsPUL gene maintained a relatively high expression level during the entire period of seed development, and peaked in the middle and late stages. This observation was very consistent with that of the endogenous transcription analysis by Q-PCR. Furthermore, the seed germination experiment showed that the OsPUL promoter actively functions in the late stage of seed germination. The expression of the OsPUL gene was maintained at a significant level during the entire grain filling period and in the late stage of seed germination, which coincided with its involvement in starch anabolism and catabolism.
淀粉去分支酶(DBEs)是参与谷物淀粉代谢的关键酶,在淀粉合成和降解中具有双重功能。然而,它们在该途径中的精确作用,尤其是它们的表达谱,仍不清楚。在本研究中,我们对编码支链淀粉酶型DBE的OsPUL基因在不同组织以及不同发育阶段种子中的表达模式进行了定量实时PCR(Q-PCR)分析。结果表明,该基因仅在种子中表达。此外,克隆了1177bp的OsPUL启动子序列,并观察到该区域存在一些胚乳特异性基序,如GCN4和AACA基序。然后将该启动子与GUS报告基因融合,并在转基因水稻中仔细研究其表达。组织化学和荧光分析的数据均表明,OsPUL启动子能够驱动靶基因进行高水平的胚乳特异性表达。OsPUL基因在种子发育的整个时期保持相对较高的表达水平,并在中后期达到峰值。这一观察结果与Q-PCR的内源转录分析结果非常一致。此外,种子萌发实验表明,OsPUL启动子在种子萌发后期发挥积极作用。OsPUL基因的表达在整个灌浆期和种子萌发后期都维持在显著水平,这与其参与淀粉合成代谢和分解代谢相一致。