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A barley cellulose synthase-like CSLH gene mediates (1,3;1,4)-beta-D-glucan synthesis in transgenic Arabidopsis

机译:大麦纤维素合成酶样CsLH基因介导转基因拟南芥中的(1,3; 1,4)-β-D-葡聚糖合成

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摘要

The walls of grasses and related members of the Poales are characterized by the presence of the polysaccharide (1,3, 1,4)-β-D-glucan (β-glucan). To date, only members of the grass-specific cellulose synthase-like F (CSLF) gene family have been implicated in its synthesis. Assuming that other grass-specific CSL genes also might encode synthases for this polysaccharide, we cloned HvCSLH1, a CSLH gene from barley (Hordeum vulgare L.), and expressed an epitope-tagged version of the cDNA in Arabidopsis, a species with no CSLH genes and no β-glucan in its walls. Transgenic Arabidopsis lines that had detectable amounts of the epitope-tagged HvCSLH1 protein accumulated β-glucan in their walls. The presence of β-glucan was confirmed by immunoelectron microscopy (immuno-EM) of sectioned tissues and chemical analysis of wall extracts. In the chemical analysis, characteristic tri- and tetra-saccharides were identified by high-performance anion-exchange chromatography and MALDI-TOF MS following their release from transgenic Arabidopsis walls by a specific β-glucan hydrolase. Immuno-EM also was used to show that the epitope-tagged HvCSLH1 protein was in the endoplasmic reticulum and Golgi-associated vesicles, but not in the plasma membrane. In barley, HvCSLH1 was expressed at very low levels in leaf, floral tissues, and the developing grain. In leaf, expression was highest in xylem and interfascicular fiber cells that have walls with secondary thickenings containing β-glucan. Thus both the CSLH and CSLF families contribute to β-glucan synthesis in grasses and probably do so independently of each other, because there is no significant transcriptional correlation between these genes in the barley tissues surveyed.
机译:草壁和Poales的相关成员的特征是多糖(1,3,1,4)-β-D-葡聚糖(β-葡聚糖)的存在。迄今为止,仅草特异性纤维素合酶样F(CSLF)基因家族的成员参与了其合成。假设其他草特异性CSL基因也可能编码该多糖的合酶,我们从大麦(Hordeum vulgare L.)克隆了HvCSLH1(一种CSLH基因),并在拟南芥中表达了cDNA的表位标签版本,该物种没有CSLH基因中没有β-葡聚糖。具有可检测量的带表位标签的HvCSLH1蛋白的转基因拟南芥品系在其壁中积累了β-葡聚糖。通过切片组织的免疫电子显微镜(immuno-EM)和壁提取物的化学分析证实了β-葡聚糖的存在。在化学分析中,通过高效的阴离子交换色谱和MALDI-TOF MS鉴定了特有的三糖和四糖,然后通过特定的β-葡聚糖水解酶将其从转基因拟南芥壁中释放出来。 Immuno-EM还可用于显示被表位标记的HvCSLH1蛋白位于内质网和高尔基体相关的囊泡中,而不位于质膜中。在大麦中,HvCSLH1在叶,花组织和发育中的谷粒中以非常低的水平表达。在叶片中,在木质部和束间纤维细胞中的表达最高,其壁具有包含β-葡聚糖的二次增厚的壁。因此,CSLH和CSLF家族都有助于草中的β-葡聚糖合成,并且可能彼此独立地起作用,因为在所调查的大麦组织中这些基因之间没有明显的转录相关性。

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