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Exploring Microtubule-Dependent Cellulose-Synthase-Complex Movement with High Precision Particle Tracking

机译:探索具有微细颗粒依赖性的纤维素合成酶复杂运动的高精度粒子跟踪。

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摘要

Cellulose synthesis at the plasma membrane is a critical process in plant growth and development. The displacement of cellulose synthase complexes (CSCs) by the rigid cellulose polymers they produce is a measure of enzyme activity. Connections between cortical microtubules and CSCs have been identified but it remains unclear how these affect CSC displacement speed. In this study, we applied a high throughput automated particle tracking method using near-total internal reflection fluorescence microscopy to measure the speed of CSCs. We found CSC speeds did not vary according to their proximity to microtubules, and that inhibiting microtubule polymerization could have opposite effects on CSC speed, depending on the nature of inhibition. While CSC speed increased in the temperature-sensitive mor1-1 mutant, it decreased after treatment with the drug oryzalin. Moreover, introducing the mor1-1 mutation into the CesA1 mutant any1 increased CSC speed, suggesting that microtubule dynamics affect CSC speed by a mechanism other than Cellulose Synthase A (CesA) catalytic activity. CSC speed varied widely in a range of mutants with reduced growth anisotropy, indicating that the relationship between CSC speed and anisotropy is complex. We conclude that microtubules affect CSC speed by finely tuned mechanisms that are independent of their physical association with CSCs.
机译:在质膜上的纤维素合成是植物生长和发育的关键过程。纤维素合酶复合物(CSC)产生的刚性纤维素聚合物取代纤维素合酶复合物(CSC)是酶活性的量度。皮层微管和CSC之间的连接已经确定,但仍不清楚它们如何影响CSC置换速度。在这项研究中,我们应用了近全内反射荧光显微镜技术的高通量自动粒子跟踪方法来测量CSC的速度。我们发现CSC速度不会因其与微管的接近程度而变化,并且抑制微管聚合可能会对CSC速度产生相反的影响,具体取决于抑制的性质。虽然温度敏感的mor1-1突变体的CSC速度增加,但在用药物米扎林治疗后速度降低。此外,将mor1-1突变引入CesA1突变体any1可以提高CSC速度,这表明微管动力学通过纤维素合成酶A(CesA)催化活性以外的机制影响CSC速度。 CSC速度在一系列具有降低的生长各向异性的突变体中变化很大,这表明CSC速度与各向异性之间的关系很复杂。我们得出的结论是,微管通过微调的机制影响CSC的速度,这种机制与其与CSC的物理关联无关。

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