首页> 外文期刊>BMC Genomics >Characterization and transcript profiling of the pectin methylesterase (PME) and pectin methylesterase inhibitor (PMEI) gene families in flax ( Linum usitatissimum )
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Characterization and transcript profiling of the pectin methylesterase (PME) and pectin methylesterase inhibitor (PMEI) gene families in flax ( Linum usitatissimum )

机译:亚麻中的果胶甲酯酶(PME)和果胶甲酯酶抑制剂(PMEI)基因家族的特征和转录谱分析

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Background Pectin methylesterases (PMEs) catalyze the demethylesterification of homogalacturonans in the cell wall; their activity is regulated in part by pectin methylesterase inhibitors (PMEIs). PME activity may result in either rigidification or loosening of the cell wall, depending on the mode of demethylesterification. The activity of PMEs in the middle lamella is expected to affect intrusive elongation of phloem fibers, and their adhesion to adjacent cells. Length and extractability of phloem fibers are qualities important for their industrial uses in textiles and composites. As only three flax PMEs had been previously described, we were motivated to characterize the PME and PMEI gene families of flax. Results We identified 105 putative flax PMEs (LuPMEs) and 95 putative PMEIs (LuPMEIs) within the whole-genome assembly. We found experimental evidence for the transcription of 77/105 LuPMEs and 83/95 LuPMEIs, and surveyed the transcript abundance of these in 12 different tissues and stages of development. Six major monophyletic groups of LuPMEs could be defined based on the inferred relationships of flax genes and their presumed orthologs from other species. We searched the LuPMEs and LuPMEIs for conserved residues previously reported to be important for their tertiary structure and function. In the LuPMEs, the most highly conserved residues were catalytic residues while in the LuPMEIs, cysteines forming disulfude bridges between helices α2 and α3 were most highly conserved. In general, the conservation of critical residues was higher in the genes with evidence of transcript expression than in those for which no expression was detected. Conclusions The LuPMEs and LuPMEIs comprise large families with complex patterns of transcript expression and a wide range of physical characteristics. We observed that multiple PMEs and PMEIs are expressed in partially overlapping domains, indicative of several genes acting redundantly during most processes. The potential for functional redundancy was highlighted also by the phylogenetic analyses. We were able to identify a subset of PME and PMEIs that appeared particularly relevant to fiber development, which may provide a basis for the improvement of key traits in industrial feedstocks and a better understanding of the physiological roles of PMEs and PMEIs in general.
机译:背景果胶甲基酯酶(PMEs)催化高半乳糖醛酸在细胞壁中的脱甲基酯化;它们的活性部分受果胶甲基酯酶抑制剂(PMEIs)调节。 PME活性可能导致细胞壁硬化或松弛,具体取决于脱甲基酯化的方式。预期中层中PME的活性会影响韧皮部纤维的侵入性伸长及其与相邻细胞的粘附。韧皮部纤维的长度和可萃取性对于它们在纺织品和复合材料中的工业用途而言是重要的品质。由于先前仅描述了三种亚麻PME,因此我们有动机来表征亚麻的PME和PMEI基因家族。结果我们在全基因组大会中确定了105个推定的亚麻PME(LuPME)和95个推定的PMEI(LuPMEI)。我们找到了77/105 LuPME和83/95 LuPMEI转录的实验证据,并调查了它们在12个不同组织和发育阶段的转录本丰度。根据亚麻基因及其与其他物种的直系同源物的推断关系,可以定义LuPME的六个主要单系群。我们在LuPME和LuPMEI中进行了搜索,以寻找先前据报道对其三级结构和功能很重要的保守残基。在LuPME中,最保守的残基是催化残基,而在LuPMEI中,在螺旋α2和α3之间形成二硫桥的半胱氨酸最保守。通常,在有转录本表达证据的基因中,关键残基的保守性高于未检测到表达的基因。结论LuPME和LuPMEI包含大家族,具有复杂的转录表达模式和广泛的物理特征。我们观察到,多个PME和PMEI在部分重叠的域中表达,表明在大多数过程中多个基因冗余发挥作用。系统发育分析也突出了功能冗余的潜力。我们能够鉴定出与纤维发展特别相关的PME和PMEI的子集,这可能为改善工业原料的关键性状和更好地理解PME和PMEI的生理作用提供基础。

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