Gao Wenwen, Lu Linghong, Qiu Wenmin, Wang Chuang, Shou Huixia
State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou, PR China.
Key Laboratory of Tree Breeding of Zhejiang Province, The Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Hangzhou, Zhejiang, PR China.
Plant Cell Physiol. 2017 May 1;58(5):885-892. doi: 10.1093/pcp/pcx041.
During phosphate (Pi) starvation or leaf senescence, the accumulation of intracellular and extracellular purple acid phosphatases (PAPs) increases in plants in order to scavenge organic phosphorus (P). In this study, we demonstrated that a PAP-encoding gene in rice, OsPAP26, is constitutively expressed in all tissues. While the abundance of OsPAP26 transcript is not affected by Pi supply, it is up-regulated during leaf senescence. Furthermore, Pi deprivation and leaf senescence greatly increased the abundance of OsPAP26 protein. Overexpression or RNA interference (RNAi) of OsPAP26 in transgenic rice significantly increased or reduced APase activities, respectively, in leaves, roots and growth medium. Compared with wild-type (WT) plants, Pi concentrations of OsPAP26-overexpressing plants increased in the non-senescing leaves and decreased in the senescing leaves. The increased remobilization of Pi from the senescing leaves to non-senescing leaves in the OsPAP26-overexpressing plants resulted in better growth performance when plants were grown in Pi-depleted condition. In contrast, OsPAP26-RNAi plants retained more Pi in the senescing leaves, and were more sensitive to Pi starvation stress. OsPAP26 was found to localize to the apoplast of rice cells. Western blot analysis of protein extracts from callus growth medium confirmed that OsPAP26 is a secreted PAP. OsPAP26-overexpressing plants were capable of converting more ATP into inorganic Pi in the growth medium, which further supported the potential role of OsPAP26 in utilizing organic P in the rhizosphere. In summary, we concluded that OsPAP26 performs dual functions in plants: Pi remobilization from senescing to non-senescing leaves; and organic P utilization.
在磷(Pi)饥饿或叶片衰老期间,植物细胞内和细胞外紫色酸性磷酸酶(PAPs)的积累会增加,以便清除有机磷(P)。在本研究中,我们证明水稻中一个编码PAP的基因OsPAP26在所有组织中组成型表达。虽然OsPAP26转录本的丰度不受Pi供应的影响,但在叶片衰老期间会上调。此外,Pi缺乏和叶片衰老极大地增加了OsPAP26蛋白的丰度。在转基因水稻中过表达或RNA干扰(RNAi)OsPAP26分别显著增加或降低了叶片、根和生长培养基中的酸性磷酸酶(APase)活性。与野生型(WT)植株相比,过表达OsPAP26的植株在未衰老叶片中的Pi浓度增加,而在衰老叶片中降低。在Pi缺乏条件下生长时,过表达OsPAP26的植株中Pi从衰老叶片向未衰老叶片的再转运增加,导致其生长性能更好。相反,OsPAP26-RNAi植株在衰老叶片中保留了更多的Pi,并且对Pi饥饿胁迫更敏感。发现OsPAP26定位于水稻细胞的质外体。对愈伤组织生长培养基中蛋白质提取物的蛋白质免疫印迹分析证实OsPAP26是一种分泌型PAP。过表达OsPAP26的植株能够在生长培养基中将更多的ATP转化为无机Pi,这进一步支持了OsPAP26在利用根际有机P方面的潜在作用。总之,我们得出结论,OsPAP26在植物中发挥双重功能:Pi从衰老叶片向未衰老叶片的再转运;以及有机P的利用。