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The GMD1 and GMD2 Genes of Arabidopsis Encode Isoforms of GDP-D-Mannose 4,6-Dehydratase with Cell Type-Specific Expression Patterns1

机译:拟南芥的GMD1和GMD2基因编码具有细胞类型特异性表达模式的GDP-D-甘露糖4,6-脱水酶同工型1

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摘要

l-Fucose (l-Fuc) is a monosaccharide constituent of plant cell wall polysaccharides and glycoproteins. The committing step in the de novo synthesis of l-Fuc is catalyzed by GDP-d-mannose 4,6-dehydratase, which, in Arabidopsis, is encoded by the GMD1 and GMD2 (MUR1) genes. To determine the functional significance of this genetic redundancy, the expression patterns of both genes were investigated via promoter-β-glucuronidase fusions and immunolocalization of a Fuc-containing epitope. GMD2 is expressed in most cell types of the root, with the notable exception of the root tip where strong expression of GMD1 is observed. Within shoot organs, GMD1::GUS expression is confined to stipules and pollen grains leading to fucosylation of the walls of these cell types in the mur1 mutant. These results suggest that GMD2 represents the major housekeeping gene for the de novo synthesis of GDP-l-Fuc, whereas GMD1 expression is limited to a number of specialized cell types. We conclude that the synthesis of GDP-l-Fuc is controlled in a cell-autonomous manner by differential expression of two isoforms of the same enzyme.
机译:1-岩藻糖(1-Fuc)是植物细胞壁多糖和糖蛋白的单糖成分。 I-Fuc从头合成的关键步骤是由GDP-d-甘露糖4,6-脱水酶催化,该酶在拟南芥中由GMD1和GMD2(MUR1)基因编码。为了确定这种遗传冗余的功能重要性,通过启动子-β-葡糖醛酸糖苷酶融合体和含Fuc的抗原决定簇的免疫定位研究了这两个基因的表达模式。 GMD2在根的大多数细胞类型中都有表达,但根尖明显例外,其中观察到GMD1的强烈表达。在芽器官中,GMD1 :: GUS表达仅限于托叶和花粉粒,从而导致mur1突变体中这些细胞类型壁的岩藻糖基化。这些结果表明,GMD2代表GDP 1-Fuc的从头合成的主要管家基因,而GMD1的表达限于许多专门的细胞类型。我们得出结论,GDP-1-Fuc的合成以细胞自主方式通过同一酶的两个同工型的差异表达来控制。

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