拟南芥气孔极性蛋白BASL介导细胞分裂前后不同的过程,协调细胞大小和命运的不对称

Yan Gong, Julien Alassimone, A. Muroyama, Gabriel O. Amador, Rachel Varnau, Ao Liu, D. Bergmann
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引用次数: 11

摘要

在许多陆地植物中,不对称细胞分裂(ACDs)在叶片表面产生分化的细胞类型。在拟南芥(Arabidopsis)气孔谱系中,气孔谱系中不对称断裂(BREAKING OF asymmetric In stomatal lineage, BASL)调控着ACD的多个方面,包括分裂面定位和细胞命运执行。BASL的极化亚细胞定位在ACD之前开始,并在两个子细胞中的一个分裂后持续数小时。解开分裂前后极化BASL各自的贡献对于更好地理解其在调节气孔谱系ACDs中的作用以及揭示指导叶片模式的规则至关重要。在这里,我们将定量成像和谱系追踪与提供暂时限制BASL表达的遗传工具结合起来。我们发现分裂前的BASL是分裂方向所必需的,而分裂后的BASL极性确保了适当的细胞命运承诺。这些基因操作使我们能够从极性新月遗传中分离出女儿细胞大小的不对称,揭示了这两种不对称对随后细胞行为的独立影响。最后,我们发现ACDs产生的姐妹细胞的分裂频率之间存在协调,这种耦合需要BASL作为肽信号的效应物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Arabidopsis stomatal polarity protein BASL mediates distinct processes before and after cell division to coordinate cell size and fate asymmetries
In many land plants, asymmetric cell divisions (ACDs) create and pattern differentiated cell types on the leaf surface. In the Arabidopsis stomatal lineage, BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) regulates multiple aspects of ACD including division plane placement and cell fate enforcement. Polarized subcellular localization of BASL is initiated before the ACD and persists for many hours after the division in one of the two daughters. Untangling the respective contributions of polarized BASL before and after division is essential to gain a better understanding of its roles in regulating stomatal lineage ACDs and to uncover the rules that guide leaf pattern. Here we combine quantitative imaging and lineage tracking with genetic tools that provide temporally-restricted BASL expression. We find that pre-division BASL is required for division orientation, whereas BASL polarity post-division ensures proper cell fate commitment. These genetic manipulations allowed us to uncouple daughter-cell size asymmetry from polarity crescent inheritance, revealing independent effects of these two asymmetries on subsequent cell behavior. Finally, we show that there is coordination between the division frequencies of sister cells produced by ACDs, and this coupling requires BASL as an effector of peptide signaling.
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