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一种用于分析水稻叶鞘中盐响应蛋白的蛋白质组学方法。

A proteomic approach to analyze salt-responsive proteins in rice leaf sheath.

作者信息

Abbasi Fida Mohammad, Komatsu Setsuko

机构信息

National Institute of Agrobiological Sciences, Kannondai 2-1-2, Tsukuba, Ibaraki 305-8602, Japan.

出版信息

Proteomics. 2004 Jul;4(7):2072-81. doi: 10.1002/pmic.200300741.

Abstract

To examine the response of rice to salt stress, changes in protein expression were analyzed using a proteomic approach. To investigate dose- and time-dependent responses, rice seedlings were exposed to 50, 100 and 150 mM NaCl for 6 to 48 h. Proteins were extracted from leaf sheath and separated by two-dimensional polyacrylamide gel electrophoresis. Eight proteins showed 1- to 3-fold up-regulation in leaf sheath, in response to 50 mM NaCl for 24 h. Among these, three proteins were unidentified (LSY081, LSY262 and LSY363) while five proteins were identified as fructose bisphosphate aldolases, photosystem II (PSII) oxygen evolving complex protein, oxygen evolving enhancer protein 2 (OEE2) and superoxide dismutase (SOD). The maximum expression levels of seven proteins were at 24 h. Their expression declined after 48 h of 50 mM NaCl treatment. In contrast, SOD maintained its elevated expression throughout these conditions. The increased expression of proteins seen in the 50 mM NaCl treatment group was less pronounced in the groups receiving 100 or 150 mM NaCl for 24 h. The expression of SOD was a common response to cold, drought, salt and abscisic acid (ABA) stresses while the expression of LSY081, LSY363 and OEE2 was enhanced by salt and ABA stresses. LSY262 was expressed in leaf sheath and root, while fructose bisphosphate aldolases, PSII oxygen evolving complex protein and OEE2 were expressed in leaf sheath and leaf blade. LSY363 was expressed in leaf sheath but was below the level of detection in leaf blade and root. These results indicate that specific proteins expressed in specific regions of rice show a coordinated response to salt stress.

摘要

为了研究水稻对盐胁迫的响应,采用蛋白质组学方法分析了蛋白质表达的变化。为了研究剂量和时间依赖性响应,将水稻幼苗暴露于50、100和150 mM NaCl中6至48小时。从叶鞘中提取蛋白质,并通过二维聚丙烯酰胺凝胶电泳进行分离。8种蛋白质在叶鞘中表现出1至3倍的上调,这是对50 mM NaCl处理24小时的响应。其中,3种蛋白质未被鉴定(LSY081、LSY262和LSY363),而5种蛋白质被鉴定为果糖二磷酸醛缩酶、光系统II(PSII)放氧复合体蛋白、放氧增强蛋白2(OEE2)和超氧化物歧化酶(SOD)。7种蛋白质的最大表达水平出现在24小时。在50 mM NaCl处理48小时后,它们的表达下降。相比之下,SOD在这些条件下始终保持其升高的表达。在50 mM NaCl处理组中观察到的蛋白质表达增加在接受100或150 mM NaCl处理24小时的组中不太明显。SOD的表达是对冷、干旱、盐和脱落酸(ABA)胁迫的共同响应,而LSY081, LSY363和OEE2的表达则受到盐和ABA胁迫的增强。LSY262在叶鞘和根中表达,而果糖二磷酸醛缩酶、PSII放氧复合体蛋白和OEE2在叶鞘和叶片中表达。LSY363在叶鞘中表达,但在叶片和根中的表达低于检测水平。这些结果表明,水稻特定区域表达的特定蛋白质对盐胁迫表现出协同响应。

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