首页> 美国卫生研究院文献>Plant Physiology >MUCILAGE-MODIFIED4 Encodes a Putative Pectin Biosynthetic Enzyme Developmentally Regulated by APETALA2 TRANSPARENT TESTA GLABRA1 and GLABRA2 in the Arabidopsis Seed Coat
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MUCILAGE-MODIFIED4 Encodes a Putative Pectin Biosynthetic Enzyme Developmentally Regulated by APETALA2 TRANSPARENT TESTA GLABRA1 and GLABRA2 in the Arabidopsis Seed Coat

机译:MUCILAGE-MODIFIED4编码拟南芥种皮中由APETALA2透明TESTA GLABRA1和GLABRA2发育调节的假定果胶生物合成酶。

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摘要

The Arabidopsis seed coat epidermis undergoes a complex process of differentiation that includes the biosynthesis and secretion of large quantities of pectinaceous mucilage, cytoplasmic rearrangement, and secondary cell wall biosynthesis. Mutations in MUM4 (MUCILAGE-MODIFIED4) lead to a decrease in seed coat mucilage and incomplete cytoplasmic rearrangement. We show that MUM4 encodes a putative NDP-l-rhamnose synthase, an enzyme required for the synthesis of the pectin rhamnogalacturonan I, the major component of Arabidopsis mucilage. This result suggests that the synthesis of monosaccharide substrates is a limiting factor in the biosynthesis of pectinaceous seed coat mucilage. In addition, the reduced cytoplasmic rearrangement observed in the absence of a key enzyme in pectin biosynthesis in mum4 mutants establishes a causal link between mucilage production and cellular morphogenesis. The cellular phenotype seen in mum4 mutants is similar to that of several transcription factors (AP2 [APETALA2], TTG1 [TRANSPARENT TESTA GLABRA1], TTG2 MYB61, and GL2 [GLABRA2]). Expression studies suggest that MUM4 is developmentally regulated in the seed coat by AP2, TTG1, and GL2, whereas TTG2 and MYB61 appear to be regulating mucilage production through alternate pathway(s). Our results provide a framework for the regulation of mucilage production and secretory cell differentiation.
机译:拟南芥种皮表皮经历了复杂的分化过程,包括生物合成和分泌大量果胶粘液,细胞质重排和次级细胞壁生物合成。 MUM4中的突变(MUCILAGE-MODIFIED4)导致种皮粘液减少和不完整的细胞质重排。我们表明,MUM4编码一个假定的NDP-1-鼠李糖合酶,一种合成果胶鼠李糖半乳糖醛酸聚糖I(拟南芥黏液的主要成分)所需的酶。该结果表明,单糖底物的合成是果胶种皮粘液生物合成中的限制因素。另外,在mum4突变体的果胶生物合成中不存在关键酶的情况下观察到的胞质重排减少,在粘液产生和细胞形态发生之间建立了因果关系。在mum4突变体中看到的细胞表型与几种转录因子(AP2 [APETALA2],TTG1 [透明TESTA GLABRA1],TTG2 MYB61和GL2 [GLABRA2])相似。表达研究表明,AP2,TTG1和GL2在种皮中对MUM4的发育有调控作用,而TTG2和 MYB61 似乎是通过其他途径调控粘液产生。我们的结果为调节粘液产生和分泌细胞分化提供了框架。

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