Gao Hui, Zhang Yinghui, Wang Wanlei, Zhao Keke, Liu Chunmei, Bai Lin, Li Rui, Guo Yi
Hebei Key Laboratory of Molecular and Cellular Biology and Key Laboratory of Molecular and Cellular Biology of the Ministry of Education, College of Life Science, Hebei Normal University, Shijia Zhuang, Hebei 050024, People's Republic of China (H.G., Y.Z., W.W., K.Z., C.L., L.B., R.L., Y.G.); and.
Hebei Collaboration Innovation Center for Cell Signaling, Shijia Zhuang, Hebei 050024, People's Republic of China (H.G., Y.Z., W.W., K.Z., C.L., L.B., R.L., Y.G.).
Plant Physiol. 2017 Jan;173(1):219-239. doi: 10.1104/pp.16.01719. Epub 2016 Nov 21.
Aspartic proteases are a class of proteolytic enzymes with conserved aspartate residues, which are implicated in protein processing, maturation, and degradation. Compared with yeast and animals, plants possess a larger aspartic protease family. However, little is known about most of these enzymes. Here, we characterized two Arabidopsis (Arabidopsis thaliana) putative glycosylphosphatidylinositol (GPI)-anchored aspartic protease genes, A36 and A39, which are highly expressed in pollen and pollen tubes. a36 and a36 a39 mutants display significantly reduced pollen activity. Transmission electron microscopy and terminal-deoxynucleotidyl transferase-mediated nick end labeling assays further revealed that the unviable pollen in a36 a39 may undergo unanticipated apoptosis-like programmed cell death. The degeneration of female gametes also occurred in a36 a39 Aniline Blue staining, scanning electron microscopy, and semi in vitro guidance assays indicated that the micropylar guidance of pollen tubes is significantly compromised in a36 a39 A36 and A39 that were fused with green fluorescent protein are localized to the plasma membrane and display punctate cytosolic localization and colocalize with the GPI-anchored protein COBRA-LIKE10. Furthermore, in a36 a39, the abundance of highly methylesterified homogalacturonans and xyloglucans was increased significantly in the apical pollen tube wall. These results indicate that A36 and A39, two putative GPI-anchored aspartic proteases, play important roles in plant reproduction in Arabidopsis.
天冬氨酸蛋白酶是一类具有保守天冬氨酸残基的蛋白水解酶,参与蛋白质加工、成熟和降解过程。与酵母和动物相比,植物拥有更大的天冬氨酸蛋白酶家族。然而,对于这些酶中的大多数,人们了解甚少。在此,我们对两个拟南芥(Arabidopsis thaliana)假定的糖基磷脂酰肌醇(GPI)锚定天冬氨酸蛋白酶基因A36和A39进行了表征,它们在花粉和花粉管中高度表达。a36和a36 a39突变体的花粉活性显著降低。透射电子显微镜和末端脱氧核苷酸转移酶介导的缺口末端标记分析进一步表明,a36 a39中无法存活的花粉可能会经历意外的凋亡样程序性细胞死亡。雌配子的退化在a36 a39中也会发生。苯胺蓝染色、扫描电子显微镜和半体外引导分析表明,a36 a39中花粉管的珠孔引导显著受损。与绿色荧光蛋白融合的A36和A39定位于质膜,呈现点状胞质定位,并与GPI锚定蛋白COBRA-LIKE10共定位。此外,在a36 a39中,顶端花粉管壁中高度甲基酯化的同型半乳糖醛酸和木葡聚糖的丰度显著增加。这些结果表明,两个假定的GPI锚定天冬氨酸蛋白酶A36和A39在拟南芥的植物繁殖中发挥重要作用。