Department of Plant Biology, University of Georgia, Athens, GA, 30602, USA.
Department of Chemistry, University of Georgia, Athens, GA, 30602, USA.
Planta. 2023 Jan 23;257(2):43. doi: 10.1007/s00425-023-04077-4.
We have demonstrated that the Arabidopsis FRA9 (fragile fiber 9) gene is specifically expressed in secondary wall-forming cells and essential for the synthesis of the unique xylan reducing end sequence. Xylan is made of a linear chain of β-1,4-linked xylosyl (Xyl) residues that are often substituted with (methyl)glucuronic acid [(Me)GlcA] side chains and may be acetylated at O-2 and/or O-3. The reducing end of xylan from gymnosperms and dicots contains a unique tetrasaccharide sequence consisting of β-D-Xylp-(1 → 3)-α-L-Rhap-(1 → 2)-α-D-GalpA-(1 → 4)-D-Xylp, the synthesis of which requires four different glycosyltransferase activities. Genetic analysis in Arabidopsis thaliana has so far implicated three glycosyltransferase genes, FRA8 (fragile fiber 8), IRX8 (irregular xylem 8) and PARVUS, in the synthesis of this unique xylan reducing end sequence. Here, we report the essential role of FRA9, a member of glycosyltransferase family 106 (GT106), in the synthesis of this sequence. The expression of the FRA9 gene was shown to be induced by secondary wall master transcriptional regulators and specifically associated with secondary wall-forming cells, including xylem and fiber cells. T-DNA knockout mutation of the FRA9 gene caused impaired secondary cell wall thickening in leaf veins and a severe arrest of plant growth. RNA interference (RNAi) downregulation of FRA9 led to a significant reduction in secondary wall thickening of fibers, a deformation of xylem vessels and a decrease in xylan content. Structural analysis of xylanase-released xylooligomers revealed that RNAi downregulation of FRA9 resulted in a diminishment of the unique xylan reducing end sequence and complete methylation of xylan GlcA side chains, chemotypes reminiscent of those of the fra8, irx8 and parvus mutants. Furthermore, two FRA9 close homologs from Populus trichocarpa were found to be wood-associated functional orthologs of FRA9. Together, our findings uncover a member of the GT106 family as a new player involved in the synthesis of the unique reducing end sequence of xylan.
我们已经证明,拟南芥 Fra9(脆弱纤维 9)基因特异性表达于次生壁形成细胞,对独特的木聚糖还原端序列的合成至关重要。木聚糖由β-1,4-连接的木糖(Xyl)残基组成的线性链组成,这些残基通常被(甲基)葡萄糖醛酸[(Me)GlcA]侧链取代,并且可能在 O-2 和/或 O-3 位乙酰化。裸子植物和双子叶植物的木聚糖还原端含有一个独特的四糖序列,由β-D-Xylp-(1 → 3)-α-L-Rhap-(1 → 2)-α-D-GalpA-(1 → 4)-D-Xylp 组成,其合成需要四种不同的糖基转移酶活性。拟南芥中的遗传分析迄今为止已经确定了三个糖基转移酶基因 Fra8(脆弱纤维 8)、IRX8(不规则木质部 8)和 PARVUS,它们参与了该独特木聚糖还原端序列的合成。在这里,我们报告了糖基转移酶家族 106(GT106)成员 Fra9 在该序列合成中的重要作用。Fra9 基因的表达受次生壁主转录调控因子诱导,并与次生壁形成细胞(包括木质部和纤维细胞)特异性相关。Fra9 基因的 T-DNA 敲除突变导致叶片叶脉次生细胞壁加厚受损和植物生长严重停滞。Fra9 的 RNAi 下调导致纤维次生壁增厚显著减少、木质部导管变形和木聚糖含量降低。木聚糖酶释放的低聚木糖的结构分析表明,Fra9 的 RNAi 下调导致独特的木聚糖还原端序列减少,木聚糖 GlcA 侧链完全甲基化,化学型类似于 fra8、irx8 和 parvus 突变体。此外,还发现毛白杨中的两个 Fra9 近同源物是 Fra9 的木质部相关功能直系同源物。总之,我们的研究结果揭示了 GT106 家族的一个新成员,它是参与木聚糖独特还原端序列合成的新成员。