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Pathways associated with lignin biosynthesis in lignomaniac jute fibres

机译:木质素黄麻纤维中木质素生物合成的相关途径

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We generated the bast transcriptomes of a deficient lignified phloem fibre mutant and its wild-type jute (Corchorus capsularis) using Illumina paired-end sequencing. A total of 34,163 wild-type and 29,463 mutant unigenes, with average lengths of 1442 and 1136 bp, respectively, were assembled de novo, similar to 77-79 % of which were functionally annotated. These annotated unigenes were assigned to COG (similar to 37-40 %) and GO (similar to 22-28 %) classifications and mapped to 189 KEGG pathways (similar to 19-21 %). We discovered 38 and 43 isoforms of 16 and 10 genes of the upstream shikimate-aromatic amino acid and downstream monolignol biosynthetic pathways, respectively, rendered their sequence similarities, confirmed the identities of 22 of these candidate gene families by phylogenetic analyses and reconstructed the pathway leading to lignin biosynthesis in jute fibres. We also identified major genes and bast-related transcription factors involved in secondary cell wall (SCW) formation. The quantitative RT-PCRs revealed that phenylalanine ammonia-lyase 1 (CcPAL1) was co-down-regulated with several genes of the upstream shikimate pathway in mutant bast tissues at an early growth stage, although its expression relapsed to the normal level at the later growth stage. However, cinnamyl alcohol dehydrogenase 7 (CcCAD7) was strongly down-regulated in mutant bast tissues irrespective of growth stages. CcCAD7 disruption at an early growth stage was accompanied by co-up-regulation of SCW-specific genes cellulose synthase A7 (CcCesA7) and fasciclin-like arabinogalactan 6 (CcFLA6), which was predicted to be involved in coordinating the S-layers' deposition in the xylan-type jute fibres. Our results identified CAD as a promising target for developing low-lignin jute fibres using genomics-assisted molecular approaches.
机译:我们使用Illumina的配对末端测序技术生成了一个不足的木质化韧皮部纤维突变体及其野生型黄麻(Corchorus荚膜猴)的韧皮转录组。从头开始组装了总共34163个野生型单基因和29463个突变单基因,平均长度分别为1442和1136 bp,与其中77-79%的功能注释相似。这些带注释的单基因被分配到COG(约占37-40%)和GO(约占22-28%)分类,并定位到189 KEGG途径(约19-21%)。我们发现上游sh草酸-芳族氨基酸和下游单木质素生物合成途径的16和10个基因的38和43个同工型,使其具有序列相似性,通过系统进化分析确认了这些候选基因家族中22个的同一性,并重建了该途径。合成黄麻纤维中的木质素。我们还确定了与次级细胞壁(SCW)形成有关的主要基因和与韧皮相关的转录因子。定量RT-PCR显示,苯丙氨酸解氨酶1(CcPAL1)在突变的韧皮组织中,与早期sh草酸途径的几个基因在生长的早期共下调,尽管其表达在后期恢复到正常水平。成长阶段。但是,肉桂醇脱氢酶7(CcCAD7)在突变韧皮组织中被强烈下调,而与生长阶段无关。 CcCAD7在早期生长阶段受到破坏,同时伴随着SCW特异基因纤维素合酶A7(CcCesA7)和fasciclin样阿拉伯半乳聚糖6(CcFLA6)的共同上调,预计这与协调S层的沉积有关在木聚糖类黄麻纤维中。我们的结果确定了CAD是使用基因组学辅助的分子方法开发低木质素黄麻纤维的有希望的目标。

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