Centre for Plant Sciences, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.
Sainsbury Laboratory, University of Cambridge, Cambridge, CB2 1LR, United Kingdom.
Plant Physiol. 2018 Feb;176(2):1547-1558. doi: 10.1104/pp.17.01568. Epub 2017 Nov 17.
A major question in plant biology concerns the specification and functional differentiation of cell types. This is in the context of constraints imposed by networks of cell walls that both adhere cells and contribute to the form and function of developing organs. Here, we report the identification of a glycan epitope that is specific to phloem sieve element cell walls in several systems. A monoclonal antibody, designated LM26, binds to the cell wall of phloem sieve elements in stems of Arabidopsis (), x , and notably sugar beet () roots where phloem identification is an important factor for the study of phloem unloading of Suc. Using microarrays of synthetic oligosaccharides, the LM26 epitope has been identified as a β-1,6-galactosyl substitution of β-1,4-galactan requiring more than three backbone residues for optimized recognition. This branched galactan structure has previously been identified in garlic () bulbs in which the LM26 epitope is widespread throughout most cell walls including those of phloem cells. Garlic bulb cell wall material has been used to confirm the association of the LM26 epitope with cell wall pectic rhamnogalacturonan-I polysaccharides. In the phloem tissues of grass stems, the LM26 epitope has a complementary pattern to that of the LM5 linear β-1,4-galactan epitope, which is detected only in companion cell walls. Mechanical probing of transverse sections of x stems and leaves by atomic force microscopy indicates that phloem sieve element cell walls have a lower indentation modulus (indicative of higher elasticity) than companion cell walls.
植物生物学中的一个主要问题涉及细胞类型的特化和功能分化。这是在细胞壁网络施加的限制背景下进行的,细胞壁不仅黏附细胞,还为发育器官的形态和功能做出贡献。在这里,我们报告了在几个系统中鉴定到一种专门存在于韧皮部筛分子细胞壁中的糖基表位。一种名为 LM26 的单克隆抗体特异性结合拟南芥(Arabidopsis)茎()、豌豆()和显著的甜菜()根中的韧皮部筛分子细胞壁,其中韧皮部鉴定是研究蔗糖从韧皮部卸载的重要因素。使用合成寡糖的微阵列,确定了 LM26 表位是β-1,6-半乳糖基取代β-1,4-半乳糖聚糖,需要三个以上的骨架残基才能实现最佳识别。这种支化半乳糖聚糖结构以前在大蒜()鳞茎中被鉴定出来,其中 LM26 表位广泛存在于包括韧皮部细胞在内的大多数细胞壁中。大蒜鳞茎细胞壁材料已被用于证实 LM26 表位与细胞壁果胶鼠李半乳糖醛酸聚糖-I 多糖的关联。在草茎的韧皮部组织中,LM26 表位与 LM5 线性β-1,4-半乳糖聚糖表位的模式互补,后者仅存在于伴胞细胞壁中。原子力显微镜对 x 茎和叶的横向切片进行机械探测表明,韧皮部筛分子细胞壁的压痕模量(表示更高的弹性)低于伴胞细胞壁。