The microtubule nucleating factor MACERATOR tethers AUGMIN7 to microtubules and governs phragmoplast architecture

Sharol Schmidt-Marcec, Alyssa Parish, Tetyana Smertenko, Matthew Hickey, Bernard M A G Piette, Andrei Smertenko
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Abstract

The plant cytokinetic microtubule array, called the phragmoplast, exhibits higher microtubule dynamics in its center (midzone) than at the periphery (distal zone). This behavior is known as the axial asymmetry. Despite being a major characteristic of the phragmoplast, little is known about regulators of this phenomenon. Here we address the role of microtubule nucleation in axial asymmetry by characterizing MACERATOR (MACET) proteins in Arabidopsis thaliana and Nicotiana benthamiana with a combination of genetic, biochemical, and live-cell imaging assays, using photo-convertible microtubule probes, and modeling. MACET paralogs accumulate at the shrinking microtubule ends and decrease the tubulin OFF rate. Loss of MACET4 and MACET5 function abrogates axial asymmetry by suppressing microtubule dynamicity in the midzone. MACET4 also narrows the microtubule nucleation angle at the phragmoplast leading edge and functions as a microtubule tethering factor for AUGMIN COMPLEX SUBUNIT 7 (AUG7). The macet4 macet5 double mutant shows diminished clustering of AUG7 in the phragmoplast distal zone. Knockout of AUG7 does not affect MACET4 localization, axial asymmetry, or microtubule nucleation angle, but increases phragmoplast length and slows down phragmoplast expansion. The mce4-1 mce5 aug7-1 triple knockout is not viable. Experimental data and modeling demonstrate that microtubule nucleation factors regulate phragmoplast architecture and axial asymmetry directly by generating new microtubules and indirectly by modulating the abundance of free tubulin.
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微管成核因子MACERATOR将AUGMIN7与微管拴在一起,并控制噬菌体结构
植物细胞运动微管阵列被称为噬菌体,其中心(中区)的微管动态高于外围(远区)。这种行为被称为轴向不对称。尽管这是膈膜的一个主要特征,但人们对这一现象的调节因素知之甚少。在这里,我们通过结合遗传、生化和活细胞成像测定,使用可光电转换的微管探针和建模,研究了拟南芥和烟草根中的 MACERATOR(MACET)蛋白,从而探讨了微管成核在轴向不对称中的作用。MACET paralogs 在收缩的微管末端聚集,并降低了微管蛋白的关闭速率。MACET4 和 MACET5 的功能缺失会抑制中区微管的动态性,从而消除轴向不对称。MACET4 还能缩小噬菌体前缘的微管成核角度,并作为 AUGMIN COMPLEX SUBUNIT 7(AUG7)的微管系链因子发挥作用。macet4 macet5 双突变体显示出 AUG7 在噬菌体远端区的集群减少。敲除 AUG7 不会影响 MACET4 的定位、轴向不对称性或微管成核角度,但会增加噬菌体的长度并减缓噬菌体的扩张。mce4-1 mce5 aug7-1 三重基因敲除不可行。实验数据和建模表明,微管成核因子直接通过产生新的微管和间接通过调节游离微管蛋白的丰度来调节噬菌体的结构和轴不对称。
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