Abstract Cell polarity is a fundamental feature underlying cell morphogenesis and organismal development. In theArabidopsisstomatal lineage, the polarity protein BASL controls stomatal asymmetric cell division. However, the cellular machinery by which this intrinsic polarity site is established remains unknown. Here, we identify the PRAF/RLD proteins as BASL physical partners and mutating fourPRAFmembers leads to defects in BASL polarization. Members of PRAF proteins are polarized in stomatal lineage cells in a BASL-dependent manner. Developmental defects of theprafmutants phenocopy those of thegnommutants. GNOM is an activator of the conserved Arf GTPases and plays important roles in membrane trafficking. We further find PRAF physically interacts with GNOM in vitro and in vivo. Thus, we propose that the positive feedback of BASL and PRAF at the plasma membrane and the connected function of PRAF and GNOM in endosomal trafficking establish intrinsic cell polarity in theArabidopsisstomatal lineage. 
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                            Quantitative and dynamic cell polarity tracking in plant cells
                        
                    
    
            Summary Quantitative information on the spatiotemporal distribution of polarised proteins is central for understanding cell‐fate determination, yet collecting sufficient data for statistical analysis is difficult to accomplish with manual measurements.Here we present Polarity Measurement (Pome), a semi‐automated pipeline for the quantification of cell polarity and demonstrate its application to a variety of developmental contexts.Pomeanalysis reveals that, during asymmetric cell divisions in theArabidopsis thalianastomatal lineage, polarity proteins BASL and BRXL2 are more asynchronous and less mutually dependent than previously thought. A similar analysis of the linearly arrayed stomatal lineage ofBrachypodium distachyonrevealed that the MAPKKK BdYDA1 is segregated and polarised following asymmetrical divisions.Our results demonstrate that Pomeis a versatile tool, which by itself or combined with tissue‐level studies and advanced microscopy techniques can help to uncover new mechanisms of cell polarity. 
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                            - Award ID(s):
- 1942722
- PAR ID:
- 10372496
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- New Phytologist
- Volume:
- 230
- Issue:
- 2
- ISSN:
- 0028-646X
- Page Range / eLocation ID:
- p. 867-877
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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