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热应激对热抗羊茅和热敏匍匐翦股颖的蛋白质组差异响应。

Differential proteomic response to heat stress in thermal Agrostis scabra and heat-sensitive Agrostis stolonifera.

机构信息

Department of Plant Biology and Pathology, Rutgers University, New Brunswick, NJ 08901, USA.

出版信息

Physiol Plant. 2010 Jun 1;139(2):192-204. doi: 10.1111/j.1399-3054.2010.01357.x. Epub 2010 Jan 25.

Abstract

Knowledge of heat-responsive proteins is critical for further understanding of the molecular mechanisms of heat tolerance. The objective of this study was to compare proteins differentially expressed in two C(3) grass species contrasting in heat tolerance, heat-tolerant thermal Agrostis scabra and heat-sensitive Agrostis stolonifera L., and to identify heat-responsive proteins for short- and long-term responses. Plants were exposed to 20/15 degrees C (day/night, control) or 40/35 degrees C (day/night, heat stress) in growth chambers. Leaves were harvested at 2 and 10 days after temperature treatment. Proteins were extracted and separated by fluorescence difference gel electrophoresis (DIGE). Thermal A. scabra had superior heat tolerance than A. stolonifera, as indicated by the maintenance of higher chlorophyll content and photochemical efficiency under heat stress. The two-dimensional difference electrophoresis detected 68 heat-responsive proteins in the two species. Thermal A. scabra had more protein spots either down- or up-regulated at 2 days of heat stress, but fewer protein spots were altered at 10 days of heat stress compared with A. stolonifera. Many protein spots exhibited transient down-regulation in thermal A. scabra (only at 2 days of heat treatment), whereas down-regulation of many proteins was also found at 10 days of heat treatment in A. stolonifera, which suggested that protein metabolism in thermal A. scabra might acclimate to heat stress more rapidly than those in A. stolonifera. The sequences of 56 differentially expressed protein spots were identified using mass spectrometry. The results suggest that the maintenance or less severe down-regulation of proteins during long-term (10 days) heat stress may contribute to the superior heat tolerance in thermal A. scabra, including those involved in photosynthesis [RuBisCo, RuBisCo activase, chloroplastic glyceraldehydes-3-phosphate dehydrogenase (GAPDH), chloroplastic aldolase, oxygen-evolving complex, photosystem I subunits], dark respiration (cytosolic GAPDH, cytoplasmic aldolase, malate dehydrogenase, hydroxypyruvate reductase, sedoheptulose-1,7-bisphosphatase), photorespiration [(hydroxypyruvate reductase, alanine aminotransferase (AlaAT), hydroxymethyltransferase (SHMT), glycine decarboxylase (GDC)], as well as heat and oxidative stress protection [heat shock cognate (HSC) 70 and FtsH-like protein].

摘要

对热响应蛋白的了解对于进一步理解耐热性的分子机制至关重要。本研究的目的是比较耐热性 C(3) 禾本科植物热 Agrostis scabra 和敏感性 Agrostis stolonifera L. 之间差异表达的蛋白质,并鉴定短期和长期响应的热响应蛋白。将植物在生长室中暴露于 20/15°C(白天/夜晚,对照)或 40/35°C(白天/夜晚,热应激)下。在温度处理后 2 和 10 天收获叶片。通过荧光差异凝胶电泳(DIGE)提取和分离蛋白质。热 A. scabra 比 A. stolonifera 具有更高的耐热性,这表现为在热应激下保持更高的叶绿素含量和光化学效率。二维差异电泳在两个物种中检测到 68 个热响应蛋白。热 A. scabra 在热应激 2 天时,无论是下调还是上调的蛋白质斑点都更多,但与 A. stolonifera 相比,热应激 10 天时改变的蛋白质斑点较少。许多蛋白质斑点在热 A. scabra 中表现出短暂的下调(仅在热处理 2 天时),而在 A. stolonifera 中,许多蛋白质的下调也发生在热处理 10 天时,这表明热 A. scabra 中的蛋白质代谢可能比 A. stolonifera 更快地适应热应激。使用质谱法鉴定了 56 个差异表达蛋白斑点的序列。结果表明,在长期(10 天)热应激期间维持或下调不太严重的蛋白质可能有助于热 A. scabra 的卓越耐热性,包括那些参与光合作用[RuBisCo、RuBisCo 激活酶、叶绿体甘油醛-3-磷酸脱氢酶(GAPDH)、叶绿体醛缩酶、氧释放复合物、光系统 I 亚基]、暗呼吸(细胞质 GAPDH、细胞质醛缩酶、苹果酸脱氢酶、羟丙酮酸还原酶、景天庚酮糖-1,7-双磷酸酶)、光呼吸[羟丙酮酸还原酶、丙氨酸氨基转移酶(AlaAT)、羟甲基转移酶(SHMT)、甘氨酸脱羧酶(GDC)],以及热和氧化应激保护[热休克同源物(HSC)70 和 FtsH 样蛋白]。

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