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Pinoresinol reductase 1 impacts lignin distribution during secondary cell wall biosynthesis in Arabidopsis

机译:松脂醇还原酶1影响拟南芥次生细胞壁生物合成过程中木质素的分布

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摘要

Pinoresinol reductase (PrR) catalyzes the conversion of the lignan (-)-pinoresinol to (-)-lariciresinol in Arabidopsis thaliana, where it is encoded by two genes, PrR1 and PrR2, that appear to act redundantly. PrR1 is highly expressed in lignified inflorescence stem tissue, whereas PrR2 expression is barely detectable in stems. Co-expression analysis has indicated that PrR1 is co-expressed with many characterized genes involved in secondary cell wall biosynthesis, whereas PrR2 expression clusters with a different set of genes. The promoter of the PrR1 gene is regulated by the secondary cell wall related transcription factors SND1 and MYB46. The loss-of-function mutant of PrR1 shows, in addition to elevated levels of pinoresinol, significantly decreased lignin content and a slightly altered lignin structure with lower abundance of cinnamyl alcohol end groups. Stimulated Raman scattering (SRS) microscopy analysis indicated that the lignin content of the prrl-1 loss-of-function mutant is similar to that of wild-type plants in xylem cells, which exhibit a normal phenotype, but is reduced in the fiber cells. Together, these data suggest an association of the lignan biosynthetic enzyme encoded by PrR1 with secondary cell wall biosynthesis in fiber cells. (C) 2014 Elsevier Ltd. All rights reserved.
机译:拟南芥中的松脂醇还原酶(PrR)催化木脂素(-)-松脂醇转化为(-)-lariciresinol,在该处它由两个基因PrR1和PrR2编码,它们似乎起着多余的作用。 PrR1在木质化的花序茎组织中高表达,而在茎中几乎检测不到PrR2表达。共表达分析表明,PrR1与次级细胞壁生物合成中涉及的许多特征基因共表达,而PrR2表达则与一组不同的基因成簇。 PrR1基因的启动子受二次细胞壁相关转录因子SND1和MYB46的调节。 PrR1的功能丧失突变体显示,除了松果醇水平升高外,木质素含量显着下降,木质素结构略有变化,肉桂醇端基的丰度较低。刺激拉曼散射(SRS)显微镜分析表明,prrl-1功能丧失突变体的木质素含量与木质部细胞中的野生型植物相似,表现出正常的表型,但在纤维细胞中却减少了。在一起,这些数据表明由PrR1编码的木脂素生物合成酶与纤维细胞中次级细胞壁生物合成的关联。 (C)2014 Elsevier Ltd.保留所有权利。

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