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A New Calmodulin-Binding Protein Expresses in the Context of Secondary Cell Wall Biosynthesis and Impacts Biomass Properties in Populus

机译:一种新的钙调蛋白结合蛋白在次生细胞壁生物合成的背景下表达并影响胡杨的生物量特性

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摘要

A greater understanding of biosynthesis, signaling and regulatory pathways involved in determining stem growth and secondary cell wall chemistry is important for enabling pathway engineering and genetic optimization of biomass properties. The present study describes a new functional role of PdIQD10, a Populus gene belonging to the IQ67-Domain1 family of IQD genes, in impacting biomass formation and chemistry. Expression studies showed that PdIQD10 has enhanced expression in developing xylem and tension-stressed tissues in Populus deltoides. Molecular dynamics simulation and yeast two-hybrid interaction experiments suggest interactions with two calmodulin proteins, CaM247 and CaM014, supporting the sequence-predicted functional role of the PdIQD10 as a calmodulin-binding protein. PdIQD10 was found to interact with specific Populus isoforms of the Kinesin Light Chain protein family, shown previously to function as microtubule-guided, cargo binding and delivery proteins in Arabidopsis. Subcellular localization studies showed that PdIQD10 localizes in the nucleus and plasma membrane regions. Promoter-binding assays suggest that a known master transcriptional regulator of secondary cell wall biosynthesis (PdWND1B) may be upstream of an HD-ZIP III gene that is in turn upstream of PdIQD10 gene in the transcriptional network. RNAi-mediated downregulation of PdIQD10 expression resulted in plants with altered biomass properties including higher cellulose, wall glucose content and greater biomass quantity. These results present evidence in support of a new functional role for an IQD gene family member, PdIQD10, in secondary cell wall biosynthesis and biomass formation in Populus.
机译:对确定茎的生长和次级细胞壁化学过程所涉及的生物合成,信号传导和调控途径的深入了解对于实现途径工程和生物质特性的遗传优化至关重要。本研究描述了PdIQD10(属于IQD基因的IQ67-Domain1家族的胡杨基因)在影响生物量形成和化学过程中的新功能。表达研究表明,PdIQD10在发育中的胡杨中木质部和张力胁迫的组织中具有增强的表达。分子动力学模拟和酵母两杂交相互作用实验表明与两种钙调蛋白蛋白CaM247和CaM014的相互作用,支持了PdIQD10作为钙调蛋白结合蛋白的序列预测功能。发现PdIQD10与Kinesin轻链蛋白家族的特定胡杨同工型相互作用,先前显示其在拟南芥中起微管引导,货物结合和转运蛋白的作用。亚细胞定位研究表明PdIQD10定位在细胞核和质膜区域。启动子结合测定表明,次级细胞壁生物合成(PdWND1B)的已知主转录调节因子可能位于HD-ZIP III基因的上游,而后者又位于转录网络中的PdIQD10基因的上游。 RNAi介导的PdIQD10表达下调导致植物生物量特性发生变化,包括更高的纤维素,壁葡萄糖含量和更大的生物量。这些结果提供了证据支持IQD基因家族成员PdIQD10在杨的次生细胞壁生物合成和生物量形成中的新功能。

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