Yin Guangkun, Xin Xia, Song Chao, Chen Xiaoling, Zhang Jinmei, Wu Shuhua, Li Ruifang, Liu Xu, Lu Xinxiong
National Genebank, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
National Genebank, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Plant Physiol Biochem. 2014 Jul;80:1-9. doi: 10.1016/j.plaphy.2014.03.006. Epub 2014 Mar 20.
Reactive oxygen species are the main contributors to seed deterioration. In order to study scavenging systems for reactive oxygen species in aged seed, we performed analyses using western blotting, real-time quantitative reverse-transcription polymerase chain reaction, high-performance liquid chromatography, and antioxidant enzyme activity analyses in artificially aged rice seeds (Oryza sativa L. cv. wanhua no.11). Aging seeds by storing them at 50 °C for 1, 9, or 17 months increased the superoxide radical and hydrogen peroxide levels and reduced the germination percentage from 99% to 92%, 55%, and 2%, respectively. The activity levels of superoxide dismutase (SOD), glutathione reductase (GR), and dehydroascorbate reductase (DHAR) did not change in aged seeds. In contrast, the activity levels of catalase (CAT), ascorbate peroxidase (APX), and monodehydroascorbate reductase (MDHAR) were significantly decreased in aged seeds, as were the expression of catalase and cytosolic ascorbate peroxidase protein. Transcript accumulation analysis showed that specific expression patterns were complex for each of the antioxidant enzyme types in the rice embryos. Overall, the expression of most genes was down-regulated, along with their protein expression. In addition, the reduction in the amount of ascorbate and glutathione was associated with the reduction in scavenging enzymes activity in aged rice embryos. Our data suggest that the depression of the antioxidant system, especially the reduction in the expression of CAT1, APX1 and MDHAR1, may be responsible for the accumulation of reactive oxygen species in artificially aged seed embryos, leading to a loss of seed vigor.
活性氧是种子劣变的主要促成因素。为了研究老化种子中活性氧的清除系统,我们利用蛋白质免疫印迹法、实时定量逆转录聚合酶链反应、高效液相色谱法以及抗氧化酶活性分析,对人工老化的水稻种子(Oryza sativa L. cv. wanhua no.11)进行了分析。将种子在50°C下储存1、9或17个月进行老化处理,结果显示超氧自由基和过氧化氢水平升高,发芽率分别从99%降至92%、55%和2%。老化种子中超氧化物歧化酶(SOD)、谷胱甘肽还原酶(GR)和脱氢抗坏血酸还原酶(DHAR)的活性水平没有变化。相反,老化种子中过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)和单脱氢抗坏血酸还原酶(MDHAR)的活性水平显著降低,过氧化氢酶和胞质抗坏血酸过氧化物酶蛋白的表达也显著降低。转录本积累分析表明,水稻胚中每种抗氧化酶类型的特定表达模式都很复杂。总体而言,大多数基因的表达以及它们的蛋白质表达均下调。此外,抗坏血酸和谷胱甘肽含量的降低与老化水稻胚中清除酶活性的降低有关。我们的数据表明,抗氧化系统的抑制,尤其是CAT1、APX1和MDHAR1表达的降低,可能是人工老化种子胚中活性氧积累的原因,导致种子活力丧失。