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This article is a Plant Cell Advance Online Publication. The date of its first appearance online is the official date of publication. The article has been edited and the authors have corrected proofs, but minor changes could be made before the final version is published. Posting this version online reduces the time to publication by several weeks. IN BRIEF Plant Cortical Microtubule Arrays: Recruitment Mechanisms in Common with Centrosomes Plant microtubules dynamically change configurations during growth and development, acting in cell division, polarity, and expansion (reviewed in Ehrhardt, 2008). In interphase cells, microtubules form parallel arrays in the plant cortex, the area just beneath the plasma membrane; the orientation of these arrays changes in different cell types, depending on cell growth and function. For example, in the rapidly expanding cells of the root tip, microtubule cortical arrays form bands transverse to the axis of elongation and assist in cell elongation. In mitotic cells, microtubule arrays change dramatically, forming a preprophase band that anticipates the plane of cell division, and then a spindle that segregates the chromosomes. In animal cells, radial microtubule arrays, such as the spindle, are organized from the centrosome, which contains microtubulenucleating proteins, including g-tubulin. The early finding that higher plants do not contain centrosomes established a longstanding mystery of how plant cells nucleate and organize microtubules independent of centrosomes. The microtubule-nucleating g-tubulin and a number of microtubuleassociated proteins are known to act in plant microtubule organization, but more factors remain to be identified. Drevensek et al. (2012) use the Arabidopsis thaliana TONNEAU1 (TON1) protein, a homolog of the human centrosome-associated protein FOP (FGFR1OP), to further probe the microtubule-organizing apparatus of plants. The authors identified TON1interacting proteins by yeast two-hybrid analysis and found a common sequence motif, the TON1 recruiting motif (TRM), which defines a protein family that has 34 members in Arabidopsis. The TRM proteins share specific sequence motifs but otherwise show substantial structural diversity. Indeed, TRM1 is a microtubule-associated protein (see figure), as are many other TRM proteins, but some TRM family members do not appear to associate with microtubules, suggesting a functional diversity that derives from the observed structural diversity. Further characterizing TRM1, the authors found that it binds directly to microtubules and mapped the TRM1 microtubule binding domain. Although TON1 colocalizes with microtubules, the authors found that it presumably does not directly bind microtubules but instead is recruited by its interaction with TRM1. Indeed, this interaction appears to be conserved in human centrosomes, where the CAP350 protein, which contains the same conserved interaction motifs as the TRM proteins, recruits FOP to the centrosome. Moreover, the authors found that Arabidopsis TON1 interacted with the conserved motifs from human CAP350 in a yeast two-hybrid assay. Thus, this work has identified an intriguing superfamily of proteins with diverse functions that remain to be explored and found a commonality in mechanisms of protein recruitment between the plant cortical microtubule arrays and the centrosome. Jennifer Mach Science Editor [email protected] REFERENCES TRM1 colocalizes with microtubules. Green fluorescent protein (GFP)-TRM1 (left) localizes to cortical microtubule arrays in petal epidermal cells. The GFP-TRM1 signal (red) colocalizes with the microtubule marker mCherry-B-tubulin 6 (green) in the overlaid image (right). Bars ¼ 10 mm. (Reprinted from Figures 4E and 4F of Drevensek et al. [2012].) Drevensek, S., Goussot, M., Duroc, Y., Christodoulidou, A., Steyaert, S., Schaefer, E., Duvernois, E., Grandjean, O., Vantard, M., Bouchez, D., and Pastuglia, M. (2012). The Arabidopsis TRM1–TON1 interaction reveals a recruitment network common to plant cortical microtubule arrays and eucaryotic centrosomes. Plant Cell 10.1105/ tpc.111.089748. Ehrhardt, D.W. (2008). Straighten up and fly right: Microtubule dynamics and organization of non-centrosomal arrays in higher plants. Curr. Opin. Cell Biol. 20: 107-116. www.plantcell.org/cgi/doi/10.1105/tpc.112.240111 The Plant Cell Preview, www.aspb.org ã 2012 American Society of Plant Biologists. All rights reserved. 1 of 1 Plant Cortical Microtubule Arrays: Recruitment Mechanisms in Common with Centrosomes Jennifer Mach Plant Cell; originally published online January 27, 2012; DOI 10.1105/tpc.112.240111 This information is current as of June 16, 2017 Permissions https://www.copyright.com/ccc/openurl.do?sid=pd_hw1532298X&issn=1532298X&WT.mc_id=pd_hw1532298X eTOCs Sign up for eTOCs at: http://www.plantcell.org/cgi/alerts/ctmain CiteTrack Alerts Sign up for CiteTrack Alerts at: http://www.plantcell.org/cgi/alerts/ctmain Subscription Information Subscription Information for The Plant Cell and Plant Physiology is available at: http://www.aspb.org/publications/subscriptions.cfm © American Society of Plant Biologists ADVANCING THE SCIENCE OF PLANT BIOLOGY