Division of Biological Sciences and Interdisciplinary Plant Group; Missouri Maize Center; University of Missouri; Columbia, MO USA.
Plant Signal Behav. 2013 Jun;8(6):e24540. doi: 10.4161/psb.24540. Epub 2013 Apr 11.
The tie-dyed1 (tdy1) and tdy2 mutants of maize exhibit leaf regions with starch hyperaccumulation and display unusual genetic interactions, suggesting they function in the same physiological process. Tdy2 encodes a putative callose synthase and is expressed in developing vascular tissues of immature leaves. Radiolabelling experiments and transmission electron microscopy (TEM) revealed symplastic trafficking within the phloem was perturbed at the companion cell/sieve element interface. Here, we show that as reported for tdy2 mutants, tdy1 yellow leaf regions display an excessive oil-droplet phenotype in the companion cells. Based on the proposed function of Tdy2 as a callose synthase, our previous work characterizing Tdy1 as a novel, transmembrane-localized protein, and the present findings, we speculate how TDY1 and TDY2 might interact to promote symplastic transport of both solutes and developmentally instructive macromolecules during vascular development at the companion cell/sieve element interface.
玉米的双色体 1(tdy1)和 tdy2 突变体表现出淀粉过度积累的叶片区域,并显示出异常的遗传相互作用,表明它们在同一生理过程中发挥作用。Tdy2 编码一个假定的胼胝质合酶,并在未成熟叶片的发育血管组织中表达。放射性标记实验和透射电子显微镜(TEM)显示,在伴细胞/筛分子界面处,韧皮部的胞质内运输受到干扰。在这里,我们表明,正如 tdy2 突变体所报道的那样,tdy1 黄化叶片区域在伴细胞中表现出过多的油滴表型。基于 Tdy2 作为胼胝质合酶的功能,我们之前的工作将 Tdy1 表征为一种新型的跨膜定位蛋白,以及目前的发现,我们推测 TDY1 和 TDY2 如何相互作用,以促进在伴细胞/筛分子界面处的血管发育过程中溶质和发育指导大分子的胞质内运输。