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首页> 外文期刊>Plant Omics >Identification of self-incompatibility related proteins in the pistil of Japanese pear [Pyrus pyrifolia (Burm.f.)] by proteome analysis
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Identification of self-incompatibility related proteins in the pistil of Japanese pear [Pyrus pyrifolia (Burm.f.)] by proteome analysis

机译:通过蛋白质组分析鉴定日本梨雌蕊中的自交不亲和相关蛋白

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The differences between stylar protein of the Japanese pear (Pyrus pyrifolia (Burm.f.)) cultivars ‘Kosui’ (S4S5) and ‘Kikusui’ (S2S4) were compared by two-dimensional difference gel electrophoresis (2-D DIGE), and were labelled and visualized with different fluorescent dyes (IC3-OSu, IC5-OSu) on a single 2-D gel. The individual different expressed proteins spots were subjected to identification. The proteins were analyzed by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF/MS) to identify proteins related to gametophytic self-incompatibility (GSI). S4-RNase and thaumatin-like protein 1 were successfully detected as expected in the pistils of ‘Kosui’ and ‘Kikusui’. S5-RNase was also detected in the pistils of ‘Kosui’. However, we could not detect S2-RNase in ‘Kikusui’ in this study, possibly because the level of expression of S2-RNase might be minuscule, or the estimated isoelectric point (pI) of S2-RNase (pI:9.26) was more basic than S4-RNase (pI: 9.17) and S5-RNase (pI: 9.01). These results indicate that proteomic studies are effective tools for detection of the expected proteins and might be helpful for finding the unknown key proteins related to the mechanism of self-incompatibility (SI) in many other SI plants.
机译:通过二维差异凝胶电泳(2-D DIGE)比较了日本梨(Pyrus pyrifolia(Burm.f.))品种'Kosui'(S4S5)和'Kikusui'(S2S4)的甾体蛋白之间的差异。标记并在单个2-D凝胶上用不同的荧光染料(IC3-OSu,IC5-OSu)可视化。对各个不同表达的蛋白质斑点进行鉴定。通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF / MS)分析蛋白质,以鉴定与配子体自我不相容性(GSI)相关的蛋白质。按预期在“ Kosui”和“ Kikusui”的雌蕊中成功检测到S4-RNase和thaumatin样蛋白1。在“ Kosui”的雌蕊中也发现了S5-RNase。然而,在这项研究中我们无法检测到“ Kikusui”中的S2-RNase,可能是因为S2-RNase的表达水平可能很小,或者S2-RNase的估计等电点(pI)(pI:9.26)更多比S4-RNase(pI:9.17)和S5-RNase(pI:9.01)碱性。这些结果表明,蛋白质组学研究是检测预期蛋白质的有效工具,并且可能有助于发现许多其他SI植物中与自身不相容性(SI)机制相关的未知关键蛋白质。

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