Rice Research Institute, Sichuan Agricultural University, Chengdu, Sichuan 611130, People's Republic of China.
State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China, Sichuan Agricultural University, Chengdu, Sichuan 611130, People's Republic of China.
Plant Physiol. 2020 Jul;183(3):1073-1087. doi: 10.1104/pp.20.00279. Epub 2020 May 6.
Grain filling is a complex agronomic trait that directly determines grain weight and quality in rice (). Nevertheless, key factors affecting grain filling remain poorly understood. Here, we identified a grain filling gene, , encoding a pyruvate kinase (PK). The loss of function of caused reduced PK activity and Suc translocation defects from source to sink in rice, which led to compromised grain filling. was constitutively expressed but had relatively higher expression levels in leaf and developing caryopsis and specific expression signals in tissues involved in Suc transport and unloading, supporting its biological function in regulation of grain filling by affecting Suc translocation. Subcellular localization analysis of OsPK3 revealed its association with mitochondria, and OsPK3 physically interacted and formed heterodimers in vivo with two other PK isozymes, OsPK1 and OsPK4. Both OsPK1 and OsPK4 localized to the mitochondria and cytosol and were recruited to the mitochondria by OsPK3. Despite their high sequence similarity, OsPK1 and OsPK4 had distinct expression patterns. As observed for , disruption of caused pleiotropic defects, while loss of function led to severely chalky grains without other obvious defects. Collectively, we revealed that two mitochondria-associated pyruvate kinase complexes, OsPK3-OsPK1/OsPK4, are involved in regulation of grain filling by stage-specific fine-tuning of Suc translocation.
灌浆是一个复杂的农艺性状,直接决定了水稻的粒重和品质。然而,影响灌浆的关键因素仍知之甚少。在这里,我们鉴定了一个灌浆基因,编码一个丙酮酸激酶(PK)。的功能丧失导致 PK 活性降低,蔗糖从源到库的转运缺陷,从而导致灌浆受损。在叶片和发育的颖果中组成型表达,但表达水平相对较高,在参与蔗糖运输和卸载的组织中具有特异性表达信号,支持其通过影响蔗糖转运来调节灌浆的生物学功能。OsPK3 的亚细胞定位分析表明其与线粒体相关,OsPK3 与另外两种 PK 同工酶 OsPK1 和 OsPK4 在体内相互作用并形成异二聚体。OsPK1 和 OsPK4 均定位于线粒体和细胞质,并被 OsPK3 募集到线粒体。尽管它们具有很高的序列相似性,但 OsPK1 和 OsPK4 的表达模式不同。与一样,的破坏导致了多种表型缺陷,而功能丧失导致严重的垩白粒,没有其他明显的缺陷。总之,我们揭示了两个与线粒体相关的丙酮酸激酶复合物 OsPK3-OsPK1/OsPK4 通过蔗糖转运的阶段性精细调控参与调节灌浆。