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韧皮部中结构P蛋白的转运。

Translocation of structural P proteins in the phloem.

作者信息

Golecki B, Schulz A, Thompson G A

机构信息

Botanisches Institut, Universität Kiel, Olshausenstrasse 40, D-24098 Kiel, Germany.

出版信息

Plant Cell. 1999 Jan;11(1):127-40. doi: 10.1105/tpc.11.1.127.

Abstract

Phloem-specific proteins (P proteins) are particularly useful markers to investigate long-distance trafficking of macromolecules in plants. In this study, genus-specific molecular probes were used in combination with intergeneric grafts to reveal the presence of a pool of translocatable P protein subunits. Immunoblot analyses demonstrated that Cucurbita spp P proteins PP1 and PP2 are translocated from Cucurbita maxima stocks and accumulate in Cucumis sativus scions. Cucurbita maxima or Cucurbita ficifolia PP1 and PP2 mRNAs were not detected in Cucumis sativus scions by either RNA gel blot analysis or reverse transcription-polymerase chain reaction, indicating that the proteins, rather than transcripts, are translocated. Tissue prints of the Cucumis sativus scion, using antibodies raised against Cucurbita maxima PP1 or PP2, detected both proteins in the fascicular phloem of the stem at points distal to the graft union and in the petiole of a developing leaf, suggesting that the proteins move within the assimilate stream toward sink tissues. Cucurbita maxima PP1 was immunolocalized by light microscopy in sieve elements of the extrafascicular phloem of Cucumis sativus scions, whereas Cucurbita maxima PP2 was detected in both sieve elements and companion cells.

摘要

韧皮部特异性蛋白(P蛋白)是研究植物中大分子长距离运输的特别有用的标记物。在本研究中,属特异性分子探针与属间嫁接相结合,以揭示可转运的P蛋白亚基库的存在。免疫印迹分析表明,南瓜属P蛋白PP1和PP2从笋瓜砧木转运并积累在黄瓜接穗中。通过RNA凝胶印迹分析或逆转录-聚合酶链反应在黄瓜接穗中均未检测到笋瓜或黑籽南瓜的PP1和PP2 mRNA,这表明转运的是蛋白质而非转录本。使用针对笋瓜PP1或PP2产生的抗体对黄瓜接穗进行组织印记,在嫁接点远端的茎束状韧皮部和发育中叶片的叶柄中均检测到这两种蛋白质,这表明这些蛋白质在同化物流中朝着库组织移动。通过光学显微镜在黄瓜接穗的束外韧皮部筛管分子中对笋瓜PP1进行了免疫定位,而在筛管分子和伴胞中均检测到了笋瓜PP2。

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Translocation of structural P proteins in the phloem.韧皮部中结构P蛋白的转运。
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