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应用生态学报 ›› 2010, Vol. 21 ›› Issue (12): 3231-3238.

• 研究报告 • 上一篇    下一篇

磷高效水稻根系对低磷胁迫响应的差异蛋白分析

郭玉春1,徐惠龙2,陈芳育1,郭陞垚3,梁义元1,梁康迳1,林文雄1**   

  1. 1福建农林大学作物遗传育种与综合利用教育部重点试验室, 福州 350002;2福建中医药大学药学院, 福州 350002;3福建省泉州市农业科学研究所, 福建泉州 362212
  • 出版日期:2010-12-18 发布日期:2010-12-18

Differential protein analysis on the root response of rice with high phosphorous uptake efficiency to low phosphorous stress.

GUO Yu-chun1, XU Hui-long2, CHEN Fang-yu1, GUO Sheng-yao3, LIANG Yi-yuan1, LIANG Kang-jing1, LIN Wen-xiong1   

  1. 1Ministry of Education Key Laboratory for Genetics, Breeding and Multiple Utilization of Crops, Fujian Agriculture and Forestry University, Fuzhou 350002, China|2College of Pharmacy, Fujian University of Traditional Chineses Medicine, Fuzhou 350002, China;3Quanzhou Institute of Agricultural Science, Quanzhou 362212, Fujian, China
  • Online:2010-12-18 Published:2010-12-18

摘要: 以IR71331为材料,通过水培试验,采用双向电泳分离不同磷浓度下(低磷浓度为0.5 mg·L-1,对照为10 mg·L-1)水稻生长3 d和6 d根系差异蛋白.结果表明:与对照相比,低磷胁迫下共有29个蛋白,其中3 d时间点有17个蛋白上调、11个下调、1个新增,6 d时间点有8个上调、19个下调、1个抑制表达、1个无明显变化
.经鉴定,其中的10个差异表达蛋白可归为信号转导相关蛋白、基因表达相关蛋白、代谢相关蛋白离子转运相关蛋白4个功能类群.信号转导相关蛋白分别为富含甘氨酸RNA结合蛋白和类似参与磷酸盐饥饿反应调控子;基因表达相关蛋白分别为推定的mRNA前体剪接因子SF2和推定的AAA蛋白酶家族FtsH;代谢相关蛋白分别为腺苷酸琥珀酸裂解酶、丝氨酸蛋白酶抑制剂(serpin)、S-腺苷蛋氨酸合成酶(SAM)和类似MYB类转录因子;离子转运相关蛋白分别为阳离子转运ATP酶和肌浆网膜蛋白.这些蛋白分别参与了信号识别、信号调控、mRNA 的剪接、信号传递、蛋白质降解、细胞体内离子转运和平衡等生理过程.其中serpin、SAM和MYB类转录因子是水稻响应低磷胁迫的关键蛋白.水稻根系对低磷胁迫存在着一个复杂的抗逆信号应答和代谢调控网络,其作用机理可以通过差异表达的蛋白质得以体现.

关键词: 水稻, 低磷胁迫, 磷高效, 蛋白质组学, 访花昆虫, 采集蜂, 时间格局, 园林植物

Abstract: A comparative proteomics analysis was performed to identify the molecular response of a rice cultivar (Oryza sative cv. ‘IRRI71331’) with high phosphorous (P) uptake efficiency to low P stress. The hydroponically grown rice plants were provided with two levels of P (0.5 mg·L-1 and 10 mg·L-1) supplied in quarter strength Kimura solution, and the root total proteins extracted on the 3rd and 6th day of treatments were separated by two-dimensional gel electrophoresis (2-DE). Comparing with the control (10 mg·L-1 of P), a total of 29 protein spots under low P stress (0.5 mg·L-1) showed differences in their relative abundance, among which, 17 were higher, 11 were lower, and 1 was novel on the 3rd day, and 8 were induced, 19 were suppressed, 1 was disappeared, and 1 had no obvious change on the 6th day. Ten differentially expressed protein spots were identified by MALDI-TOF/MS, and searched in protein databases. According to the putative functions, the identified proteins were classified into four groups, i.e., signal transduction (glycine-rich RNA-binding protein, phosphate starvation response regulator-like), gene expression (putative pre-mRNA splicing factor, putative AAA-metalloprotease), metabolism (adenylosuccinate lyase, serpin, S-adenosylmethionine synthetase, MYB transcription factor-like protein), and ion transport (cation-transporting ATPase, sarcoplasmic reticulum protein). The identified proteins were involved in various physiological responses to enhance stress resistance, such as signal recognition and transduction, RNA cleavage, degradation of denatured protein, and ion transportation and cellular ion balance. The serine protease inhibitor and S-adenosylmethionine synthetase and the MYB transcription factor-like protein, which were the key proteins associated with P deficiency- tolerance of other species, were affected by the same stress for rice. The results indicated that the tolerance to low P stress was controlled by a complex signal transduction and metabolism regulation network in rice root system.

Key words: rice, low phosphorous stress, high phosphorous efficiency, proteomics, flower-visiting insect, forager, temporal pattern, landscape plant.