@phdthesis{8822,
  abstract     = {Self-organization is a hallmark of plant development manifested e.g. by intricate leaf vein patterns, flexible formation of vasculature during organogenesis or its regeneration following wounding. Spontaneously arising channels transporting the phytohormone auxin, created by coordinated polar localizations of PIN-FORMED 1 (PIN1) auxin exporter, provide positional cues for these as well as other plant patterning processes. To find regulators acting downstream of auxin and the TIR1/AFB auxin signaling pathway essential for PIN1 coordinated polarization during auxin canalization, we performed microarray experiments. Besides the known components of general PIN polarity maintenance, such as PID and PIP5K kinases, we identified and characterized a new regulator of auxin canalization, the transcription factor WRKY DNA-BINDING PROTEIN 23 (WRKY23).
Next, we designed a subsequent microarray experiment to further uncover other molecular players, downstream of auxin-TIR1/AFB-WRKY23 involved in the regulation of auxin-mediated PIN repolarization. We identified a novel and crucial part of the molecular machinery underlying auxin canalization. The auxin-regulated malectin-type receptor-like kinase CAMEL and the associated leucine-rich repeat receptor-like kinase CANAR target and directly phosphorylate PIN auxin transporters. camel and canar mutants are impaired in PIN1 subcellular trafficking and auxin-mediated repolarization leading to defects in auxin transport, ultimately to leaf venation and vasculature regeneration defects. Our results describe the CAMEL-CANAR receptor complex, which is required for auxin feed-back on its own transport and thus for coordinated tissue polarization during auxin canalization.},
  author       = {Hajny, Jakub},
  issn         = {2663-337X},
  pages        = {249},
  publisher    = {Institute of Science and Technology Austria},
  title        = {{Identification and characterization of the molecular machinery of auxin-dependent canalization during vasculature formation and regeneration}},
  doi          = {10.15479/AT:ISTA:8822},
  year         = {2020},
}

@article{8943,
  abstract     = {The widely used non-steroidal anti-inflammatory drugs (NSAIDs) are derivatives of the phytohormone salicylic acid (SA). SA is well known to regulate plant immunity and development, whereas there have been few reports focusing on the effects of NSAIDs in plants. Our studies here reveal that NSAIDs exhibit largely overlapping physiological activities to SA in the model plant Arabidopsis. NSAID treatments lead to shorter and agravitropic primary roots and inhibited lateral root organogenesis. Notably, in addition to the SA-like action, which in roots involves binding to the protein phosphatase 2A (PP2A), NSAIDs also exhibit PP2A-independent effects. Cell biological and biochemical analyses reveal that many NSAIDs bind directly to and inhibit the chaperone activity of TWISTED DWARF1, thereby regulating actin cytoskeleton dynamics and subsequent endosomal trafficking. Our findings uncover an unexpected bioactivity of human pharmaceuticals in plants and provide insights into the molecular mechanism underlying the cellular action of this class of anti-inflammatory compounds.},
  author       = {Tan, Shutang and Di Donato, Martin and Glanc, Matous and Zhang, Xixi and Klíma, Petr and Liu, Jie and Bailly, Aurélien and Ferro, Noel and Petrášek, Jan and Geisler, Markus and Friml, Jiří},
  issn         = {22111247},
  journal      = {Cell Reports},
  number       = {9},
  publisher    = {Elsevier},
  title        = {{Non-steroidal anti-inflammatory drugs target TWISTED DWARF1-regulated actin dynamics and auxin transport-mediated plant development}},
  doi          = {10.1016/j.celrep.2020.108463},
  volume       = {33},
  year         = {2020},
}

@article{8986,
  abstract     = {Flowering plants display the highest diversity among plant species and have notably shaped terrestrial landscapes. Nonetheless, the evolutionary origin of their unprecedented morphological complexity remains largely an enigma. Here, we show that the coevolution of cis-regulatory and coding regions of PIN-FORMED (PIN) auxin transporters confined their expression to certain cell types and directed their subcellular localization to particular cell sides, which together enabled dynamic auxin gradients across tissues critical to the complex architecture of flowering plants. Extensive intraspecies and interspecies genetic complementation experiments with PINs from green alga up to flowering plant lineages showed that PIN genes underwent three subsequent, critical evolutionary innovations and thus acquired a triple function to regulate the development of three essential components of the flowering plant Arabidopsis: shoot/root, inflorescence, and floral organ. Our work highlights the critical role of functional innovations within the PIN gene family as essential prerequisites for the origin of flowering plants.},
  author       = {Zhang, Yuzhou and Rodriguez Solovey, Lesia and Li, Lanxin and Zhang, Xixi and Friml, Jiří},
  issn         = {2375-2548},
  journal      = {Science Advances},
  number       = {50},
  publisher    = {AAAS},
  title        = {{Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants}},
  doi          = {10.1126/sciadv.abc8895},
  volume       = {6},
  year         = {2020},
}

@article{6997,
  author       = {Zhang, Yuzhou and Friml, Jiří},
  issn         = {1469-8137},
  journal      = {New Phytologist},
  number       = {3},
  pages        = {1049--1052},
  publisher    = {Wiley},
  title        = {{Auxin guides roots to avoid obstacles during gravitropic growth}},
  doi          = {10.1111/nph.16203},
  volume       = {225},
  year         = {2020},
}

@article{7142,
  abstract     = {The phytohormone auxin acts as an amazingly versatile coordinator of plant growth and development. With its morphogen-like properties, auxin controls sites and timing of differentiation and/or growth responses both, in quantitative and qualitative terms. Specificity in the auxin response depends largely on distinct modes of signal transmission, by which individual cells perceive and convert auxin signals into a remarkable diversity of responses. The best understood, or so-called canonical mechanism of auxin perception ultimately results in variable adjustments of the cellular transcriptome, via a short, nuclear signal transduction pathway. Additional findings that accumulated over decades implied that an additional, presumably, cell surface-based auxin perception mechanism mediates very rapid cellular responses and decisively contributes to the cell's overall hormonal response. Recent investigations into both, nuclear and cell surface auxin signalling challenged this assumed partition of roles for different auxin signalling pathways and revealed an unexpected complexity in transcriptional and non-transcriptional cellular responses mediated by auxin.},
  author       = {Gallei, Michelle C and Luschnig, Christian and Friml, Jiří},
  issn         = {1879-0356},
  journal      = {Current Opinion in Plant Biology},
  number       = {2},
  pages        = {43--49},
  publisher    = {Elsevier},
  title        = {{Auxin signalling in growth: Schrödinger's cat out of the bag}},
  doi          = {10.1016/j.pbi.2019.10.003},
  volume       = {53},
  year         = {2020},
}

@article{7204,
  abstract     = {Plant root architecture dynamically adapts to various environmental conditions, such as salt‐containing soil. The phytohormone abscisic acid (ABA) is involved among others also in these developmental adaptations, but the underlying molecular mechanism remains elusive. Here, a novel branch of the ABA signaling pathway in Arabidopsis involving PYR/PYL/RCAR (abbreviated as PYLs) receptor‐protein phosphatase 2A (PP2A) complex that acts in parallel to the canonical PYLs‐protein phosphatase 2C (PP2C) mechanism is identified. The PYLs‐PP2A signaling modulates root gravitropism and lateral root formation through regulating phytohormone auxin transport. In optimal conditions, PYLs ABA receptor interacts with the catalytic subunits of PP2A, increasing their phosphatase activity and thus counteracting PINOID (PID) kinase‐mediated phosphorylation of PIN‐FORMED (PIN) auxin transporters. By contrast, in salt and osmotic stress conditions, ABA binds to PYLs, inhibiting the PP2A activity, which leads to increased PIN phosphorylation and consequently modulated directional auxin transport leading to adapted root architecture. This work reveals an adaptive mechanism that may flexibly adjust plant root growth to withstand saline and osmotic stresses. It occurs via the cross‐talk between the stress hormone ABA and the versatile developmental regulator auxin.},
  author       = {Li, Yang and Wang, Yaping and Tan, Shutang and Li, Zhen and Yuan, Zhi and Glanc, Matous and Domjan, David and Wang, Kai and Xuan, Wei and Guo, Yan and Gong, Zhizhong and Friml, Jiří and Zhang, Jing},
  issn         = {2198-3844},
  journal      = {Advanced Science},
  number       = {3},
  publisher    = {Wiley},
  title        = {{Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex}},
  doi          = {10.1002/advs.201901455},
  volume       = {7},
  year         = {2020},
}

@article{7219,
  abstract     = {Root system architecture (RSA), governed by the phytohormone auxin, endows plants with an adaptive advantage in particular environments. Using geographically representative arabidopsis (Arabidopsis thaliana) accessions as a resource for GWA mapping, Waidmann et al. and Ogura et al. recently identified two novel components involved in modulating auxin-mediated RSA and conferring plant fitness in particular habitats.},
  author       = {Xiao, Guanghui and Zhang, Yuzhou},
  issn         = {13601385},
  journal      = {Trends in Plant Science},
  number       = {2},
  pages        = {P121--123},
  publisher    = {Elsevier},
  title        = {{Adaptive growth: Shaping auxin-mediated root system architecture}},
  doi          = {10.1016/j.tplants.2019.12.001},
  volume       = {25},
  year         = {2020},
}

@article{7416,
  abstract     = {Earlier, we demonstrated that transcript levels of METAL TOLERANCE PROTEIN2 (MTP2) and of HEAVY METAL ATPase2 (HMA2) increase strongly in roots of Arabidopsis upon prolonged zinc (Zn) deficiency and respond to shoot physiological Zn status, and not to the local Zn status in roots. This provided evidence for shoot-to-root communication in the acclimation of plants to Zn deficiency. Zn-deficient soils limit both the yield and quality of agricultural crops and can result in clinically relevant nutritional Zn deficiency in human populations. Implementing Zn deficiency during cultivation of the model plant Arabidopsis thaliana on agar-solidified media is difficult because trace element contaminations are present in almost all commercially available agars. Here, we demonstrate root morphological acclimations to Zn deficiency on agar-solidified medium following the effective removal of contaminants. These advancements allow reproducible phenotyping toward understanding fundamental plant responses to deficiencies of Zn and other essential trace elements.},
  author       = {Sinclair, Scott A and Krämer, U.},
  issn         = {1559-2324},
  journal      = {Plant Signaling & Behavior},
  number       = {1},
  publisher    = {Taylor & Francis},
  title        = {{Generation of effective zinc-deficient agar-solidified media allows identification of root morphology changes in response to zinc limitation}},
  doi          = {10.1080/15592324.2019.1687175},
  volume       = {15},
  year         = {2020},
}

@article{7417,
  abstract     = {Previously, we reported that the allelic de-etiolated by zinc (dez) and trichome birefringence (tbr) mutants exhibit photomorphogenic development in the dark, which is enhanced by high Zn. TRICHOME BIREFRINGENCE-LIKE proteins had been implicated in transferring acetyl groups to various hemicelluloses. Pectin O-acetylation levels were lower in dark-grown dez seedlings than in the wild type. We observed Zn-enhanced photomorphogenesis in the dark also in the reduced wall acetylation 2 (rwa2-3) mutant, which exhibits lowered O-acetylation levels of cell wall macromolecules including pectins and xyloglucans, supporting a role for cell wall macromolecule O-acetylation in the photomorphogenic phenotypes of rwa2-3 and dez. Application of very short oligogalacturonides (vsOGs) restored skotomorphogenesis in dark-grown dez and rwa2-3. Here we demonstrate that in dez, O-acetylation of non-pectin cell wall components, notably of xyloglucan, is enhanced. Our results highlight the complexity of cell wall homeostasis and indicate against an influence of xyloglucan O-acetylation on light-dependent seedling development.},
  author       = {Sinclair, Scott A and Gille, S. and Pauly, M. and Krämer, U.},
  issn         = {1559-2324},
  journal      = {Plant Signaling & Behavior},
  number       = {1},
  publisher    = {Informa UK Limited},
  title        = {{Regulation of acetylation of plant cell wall components is complex and responds to external stimuli}},
  doi          = {10.1080/15592324.2019.1687185},
  volume       = {15},
  year         = {2020},
}

@article{7427,
  abstract     = {Plants, like other multicellular organisms, survive through a delicate balance between growth and defense against pathogens. Salicylic acid (SA) is a major defense signal in plants, and the perception mechanism as well as downstream signaling activating the immune response are known. Here, we identify a parallel SA signaling that mediates growth attenuation. SA directly binds to A subunits of protein phosphatase 2A (PP2A), inhibiting activity of this complex. Among PP2A targets, the PIN2 auxin transporter is hyperphosphorylated in response to SA, leading to changed activity of this important growth regulator. Accordingly, auxin transport and auxin-mediated root development, including growth, gravitropic response, and lateral root organogenesis, are inhibited. This study reveals how SA, besides activating immunity, concomitantly attenuates growth through crosstalk with the auxin distribution network. Further analysis of this dual role of SA and characterization of additional SA-regulated PP2A targets will provide further insights into mechanisms maintaining a balance between growth and defense.},
  author       = {Tan, Shutang and Abas, Melinda F and Verstraeten, Inge and Glanc, Matous and Molnar, Gergely and Hajny, Jakub and Lasák, Pavel and Petřík, Ivan and Russinova, Eugenia and Petrášek, Jan and Novák, Ondřej and Pospíšil, Jiří and Friml, Jiří},
  issn         = {09609822},
  journal      = {Current Biology},
  number       = {3},
  pages        = {381--395.e8},
  publisher    = {Cell Press},
  title        = {{Salicylic acid targets protein phosphatase 2A to attenuate growth in plants}},
  doi          = {10.1016/j.cub.2019.11.058},
  volume       = {30},
  year         = {2020},
}

@article{7465,
  abstract     = {The flexible development of plants is characterized by a high capacity for post-embryonic organ formation and tissue regeneration, processes, which require tightly regulated intercellular communication and coordinated tissue (re-)polarization. The phytohormone auxin, the main driver for these processes, is able to establish polarized auxin transport channels, which are characterized by the expression and polar, subcellular localization of the PIN1 auxin transport proteins. These channels are demarcating the position of future vascular strands necessary for organ formation and tissue regeneration. Major progress has been made in the last years to understand how PINs can change their polarity in different contexts and thus guide auxin flow through the plant. However, it still remains elusive how auxin mediates the establishment of auxin conducting channels and the formation of vascular tissue and which cellular processes are involved. By the means of sophisticated regeneration experiments combined with local auxin applications in Arabidopsis thaliana inflorescence stems we show that (i) PIN subcellular dynamics, (ii) PIN internalization by clathrin-mediated trafficking and (iii) an intact actin cytoskeleton required for post-endocytic trafficking are indispensable for auxin channel formation, de novo vascular formation and vascular regeneration after wounding. These observations provide novel insights into cellular mechanism of coordinated tissue polarization during auxin canalization.},
  author       = {Mazur, Ewa and Gallei, Michelle C and Adamowski, Maciek and Han, Huibin and Robert, Hélène S. and Friml, Jiří},
  issn         = {18732259},
  journal      = {Plant Science},
  number       = {4},
  publisher    = {Elsevier},
  title        = {{Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization and vascular tissue formation in Arabidopsis}},
  doi          = {10.1016/j.plantsci.2020.110414},
  volume       = {293},
  year         = {2020},
}

@article{7490,
  abstract     = {In plants, clathrin mediated endocytosis (CME) represents the major route for cargo internalisation from the cell surface. It has been assumed to operate in an evolutionary conserved manner as in yeast and animals. Here we report characterisation of ultrastructure, dynamics and mechanisms of plant CME as allowed by our advancement in electron microscopy and quantitative live imaging techniques. Arabidopsis CME appears to follow the constant curvature model and the bona fide CME population generates vesicles of a predominantly hexagonal-basket type; larger and with faster kinetics than in other models. Contrary to the existing paradigm, actin is dispensable for CME events at the plasma membrane but plays a unique role in collecting endocytic vesicles, sorting of internalised cargos and directional endosome movement that itself actively promote CME events. Internalized vesicles display a strongly delayed and sequential uncoating. These unique features highlight the independent evolution of the plant CME mechanism during the autonomous rise of multicellularity in eukaryotes.},
  author       = {Narasimhan, Madhumitha and Johnson, Alexander J and Prizak, Roshan and Kaufmann, Walter and Tan, Shutang and Casillas Perez, Barbara E and Friml, Jiří},
  issn         = {2050-084X},
  journal      = {eLife},
  publisher    = {eLife Sciences Publications},
  title        = {{Evolutionarily unique mechanistic framework of clathrin-mediated endocytosis in plants}},
  doi          = {10.7554/eLife.52067},
  volume       = {9},
  year         = {2020},
}

@article{7497,
  abstract     = {Endophytic fungi can be beneficial to plant growth. However, the molecular mechanisms underlying colonization of Acremonium spp. remain unclear. In this study, a novel endophytic Acremonium strain was isolated from the buds of Panax notoginseng and named Acremonium sp. D212. The Acremonium sp. D212 could colonize the roots of P. notoginseng, enhance the resistance of P. notoginseng to root rot disease, and promote root growth and saponin biosynthesis in P. notoginseng. Acremonium sp. D212 could secrete indole‐3‐acetic acid (IAA) and jasmonic acid (JA), and inoculation with the fungus increased the endogenous levels of IAA and JA in P. notoginseng. Colonization of the Acremonium sp. D212 in the roots of the rice line Nipponbare was dependent on the concentration of methyl jasmonate (MeJA) (2 to 15 μM) and 1‐naphthalenacetic acid (NAA) (10 to 20 μM). Moreover, the roots of the JA signalling‐defective coi1‐18 mutant were colonized by Acremonium sp. D212 to a lesser degree than those of the wild‐type Nipponbare and miR393b‐overexpressing lines, and the colonization was rescued by MeJA but not by NAA. It suggests that the cross‐talk between JA signalling and the auxin biosynthetic pathway plays a crucial role in the colonization of Acremonium sp. D212 in host plants.},
  author       = {Han, L and Zhou, X and Zhao, Y and Zhu, S and Wu, L and He, Y and Ping, X and Lu, X and Huang, W and Qian, J and Zhang, L and Jiang, X and Zhu, D and Luo, C and Li, S and Dong, Q and Fu, Q and Deng, K and Wang, X and Wang, L and Peng, S and Wu, J and Li, W and Friml, Jiří and Zhu, Y and He, X and Du, Y},
  issn         = {1744-7909},
  journal      = {Journal of Integrative Plant Biology},
  number       = {9},
  pages        = {1433--1451},
  publisher    = {Wiley},
  title        = {{Colonization of endophyte Acremonium sp. D212 in Panax notoginseng and rice mediated by auxin and jasmonic acid}},
  doi          = {10.1111/jipb.12905},
  volume       = {62},
  year         = {2020},
}

@article{7500,
  abstract     = {Plant survival depends on vascular tissues, which originate in a self‐organizing manner as strands of cells co‐directionally transporting the plant hormone auxin. The latter phenomenon (also known as auxin canalization) is classically hypothesized to be regulated by auxin itself via the effect of this hormone on the polarity of its own intercellular transport. Correlative observations supported this concept, but molecular insights remain limited.
In the current study, we established an experimental system based on the model Arabidopsis thaliana, which exhibits auxin transport channels and formation of vasculature strands in response to local auxin application.
Our methodology permits the genetic analysis of auxin canalization under controllable experimental conditions. By utilizing this opportunity, we confirmed the dependence of auxin canalization on a PIN‐dependent auxin transport and nuclear, TIR1/AFB‐mediated auxin signaling. We also show that leaf venation and auxin‐mediated PIN repolarization in the root require TIR1/AFB signaling.
Further studies based on this experimental system are likely to yield better understanding of the mechanisms underlying auxin transport polarization in other developmental contexts.},
  author       = {Mazur, E and Kulik, Ivan and Hajny, Jakub and Friml, Jiří},
  issn         = {1469-8137},
  journal      = {New Phytologist},
  number       = {5},
  pages        = {1375--1383},
  publisher    = {Wiley},
  title        = {{Auxin canalization and vascular tissue formation by TIR1/AFB-mediated auxin signaling in arabidopsis}},
  doi          = {10.1111/nph.16446},
  volume       = {226},
  year         = {2020},
}

@article{7540,
  abstract     = { In vitro propagation of the ornamentally interesting species Wikstroemia gemmata is limited by the recalcitrance to form adventitious roots. In this article, two strategies to improve the rooting capacity of in vitro microcuttings are presented. Firstly, the effect of exogenous auxin was evaluated in both light and dark cultivated stem segments and also the sucrose-content of the medium was varied in order to determine better rooting conditions. Secondly, different spectral lights were evaluated and the effect on shoot growth and root induction demonstrated that the exact spectral composition of light is important for successful in vitro growth and development of Wikstroemia gemmata. We show that exogenous auxin cannot compensate for the poor rooting under unfavorable light conditions. Adapting the culture conditions is therefore paramount for successful industrial propagation of Wikstroemia gemmata. },
  author       = {Verstraeten, Inge and Buyle, H. and Werbrouck, S. and Van Labeke, M.C. and Geelen, D.},
  issn         = {2223-8980},
  journal      = {Israel Journal of Plant Sciences},
  number       = {1-2},
  pages        = {16--26},
  publisher    = {Brill},
  title        = {{In vitro shoot growth and adventitious rooting of Wikstroemia gemmata depends on light quality}},
  doi          = {10.1163/22238980-20191110},
  volume       = {67},
  year         = {2020},
}

@article{7582,
  abstract     = {Small RNAs (smRNA, 19–25 nucleotides long), which are transcribed by RNA polymerase II, regulate the expression of genes involved in a multitude of processes in eukaryotes. miRNA biogenesis and the proteins involved in the biogenesis pathway differ across plant and animal lineages. The major proteins constituting the biogenesis pathway, namely, the Dicers (DCL/DCR) and Argonautes (AGOs), have been extensively studied. However, the accessory proteins (DAWDLE (DDL), SERRATE (SE), and TOUGH (TGH)) of the pathway that differs across the two lineages remain largely uncharacterized. We present the first detailed report on the molecular evolution and divergence of these proteins across eukaryotes. Although DDL is present in eukaryotes and prokaryotes, SE and TGH appear to be specific to eukaryotes. The addition/deletion of specific domains and/or domain-specific sequence divergence in the three proteins points to the observed functional divergence of these proteins across the two lineages, which correlates with the differences in miRNA length across the two lineages. Our data enhance the current understanding of the structure–function relationship of these proteins and reveals previous unexplored crucial residues in the three proteins that can be used as a basis for further functional characterization. The data presented here on the number of miRNAs in crown eukaryotic lineages are consistent with the notion of the expansion of the number of miRNA-coding genes in animal and plant lineages correlating with organismal complexity. Whether this difference in functionally correlates with the diversification (or presence/absence) of the three proteins studied here or the miRNA signaling in the plant and animal lineages is unclear. Based on our results of the three proteins studied here and previously available data concerning the evolution of miRNA genes in the plant and animal lineages, we believe that miRNAs probably evolved once in the ancestor to crown eukaryotes and have diversified independently in the eukaryotes.},
  author       = {Moturu, Taraka Ramji and Sinha, Sansrity and Salava, Hymavathi and Thula, Sravankumar and Nodzyński, Tomasz and Vařeková, Radka Svobodová and Friml, Jiří and Simon, Sibu},
  issn         = {22237747},
  journal      = {Plants},
  number       = {3},
  publisher    = {MDPI},
  title        = {{Molecular evolution and diversification of proteins involved in miRNA maturation pathway}},
  doi          = {10.3390/plants9030299},
  volume       = {9},
  year         = {2020},
}

@article{7600,
  abstract     = {Directional intercellular transport of the phytohormone auxin mediated by PIN FORMED (PIN) efflux carriers plays essential roles in both coordinating patterning processes and integrating multiple external cues by rapidly redirecting auxin fluxes. Multilevel regulations of PIN activity under internal and external cues are complicated; however, the underlying molecular mechanism remains elusive. Here we demonstrate that 3’-Phosphoinositide-Dependent Protein Kinase1 (PDK1), which is conserved in plants and mammals, functions as a molecular hub integrating the upstream lipid signalling and the downstream substrate activity through phosphorylation. Genetic analysis uncovers that loss-of-function Arabidopsis mutant pdk1.1 pdk1.2 exhibits a plethora of abnormalities in organogenesis and growth, due to the defective PIN-dependent auxin transport. Further cellular and biochemical analyses reveal that PDK1 phosphorylates D6 Protein Kinase to facilitate its activity towards PIN proteins. Our studies establish a lipid-dependent phosphorylation cascade connecting membrane composition-based cellular signalling with plant growth and patterning by regulating morphogenetic auxin fluxes.},
  author       = {Tan, Shutang and Zhang, Xixi and Kong, Wei and Yang, Xiao-Li and Molnar, Gergely and Vondráková, Zuzana and Filepová, Roberta and Petrášek, Jan and Friml, Jiří and Xue, Hong-Wei},
  issn         = {20550278},
  journal      = {Nature Plants},
  pages        = {556--569},
  publisher    = {Springer Nature},
  title        = {{The lipid code-dependent phosphoswitch PDK1–D6PK activates PIN-mediated auxin efflux in Arabidopsis}},
  doi          = {10.1038/s41477-020-0648-9},
  volume       = {6},
  year         = {2020},
}

@unpublished{7601,
  abstract     = {Plasmodesmata (PD) are crucial structures for intercellular communication in multicellular plants with remorins being their crucial plant-specific structural and functional constituents. The PD biogenesis is an intriguing but poorly understood process. By expressing an Arabidopsis remorin protein in mammalian cells, we have reconstituted a PD-like filamentous structure, termed remorin filament (RF), connecting neighboring cells physically and physiologically. Notably, RFs are capable of transporting macromolecules intercellularly, in a way similar to plant PD. With further super-resolution microscopic analysis and biochemical characterization, we found that RFs are also composed of actin filaments, forming the core skeleton structure, aligned with the remorin protein. This unique heterologous filamentous structure might explain the molecular mechanism for remorin function as well as PD construction. Furthermore, remorin protein exhibits a specific distribution manner in the plasma membrane in mammalian cells, representing a lipid nanodomain, depending on its lipid modification status. Our studies not only provide crucial insights into the mechanism of PD biogenesis, but also uncovers unsuspected fundamental mechanistic and evolutionary links between intercellular communication systems of plants and animals.},
  author       = {Wei, Zhuang and Tan, Shutang and Liu, Tao and Wu, Yuan and Lei, Ji-Gang and Chen, ZhengJun and Friml, Jiří and Xue, Hong-Wei and Liao, Kan},
  booktitle    = {bioRxiv},
  pages        = {22},
  publisher    = {Cold Spring Harbor Laboratory},
  title        = {{Plasmodesmata-like intercellular connections by plant remorin in animal cells}},
  doi          = {10.1101/791137},
  year         = {2020},
}

@article{7619,
  abstract     = {Cell polarity is a fundamental feature of all multicellular organisms. In plants, prominent cell polarity markers are PIN auxin transporters crucial for plant development. To identify novel components involved in cell polarity establishment and maintenance, we carried out a forward genetic screening with PIN2:PIN1-HA;pin2 Arabidopsis plants, which ectopically express predominantly basally localized PIN1 in the root epidermal cells leading to agravitropic root growth. From the screen, we identified the regulator of PIN polarity 12 (repp12) mutation, which restored gravitropic root growth and caused PIN1-HA polarity switch from basal to apical side of root epidermal cells. Complementation experiments established the repp12 causative mutation as an amino acid substitution in Aminophospholipid ATPase3 (ALA3), a phospholipid flippase with predicted function in vesicle formation. ala3 T-DNA mutants show defects in many auxin-regulated processes, in asymmetric auxin distribution and in PIN trafficking. Analysis of quintuple and sextuple mutants confirmed a crucial role of ALA proteins in regulating plant development and in PIN trafficking and polarity. Genetic and physical interaction studies revealed that ALA3 functions together with GNOM and BIG3 ARF GEFs. Taken together, our results identified ALA3 flippase as an important interactor and regulator of ARF GEF functioning in PIN polarity, trafficking and auxin-mediated development.},
  author       = {Zhang, Xixi and Adamowski, Maciek and Marhavá, Petra and Tan, Shutang and Zhang, Yuzhou and Rodriguez Solovey, Lesia and Zwiewka, Marta and Pukyšová, Vendula and Sánchez, Adrià Sans and Raxwal, Vivek Kumar and Hardtke, Christian S. and Nodzynski, Tomasz and Friml, Jiří},
  issn         = {1532-298X},
  journal      = {The Plant Cell},
  number       = {5},
  pages        = {1644--1664},
  publisher    = {American Society of Plant Biologists},
  title        = {{Arabidopsis flippases cooperate with ARF GTPase exchange factors to regulate the trafficking and polarity of PIN auxin transporters}},
  doi          = {10.1105/tpc.19.00869},
  volume       = {32},
  year         = {2020},
}

@article{7643,
  author       = {Han, Huibin and Rakusova, Hana and Verstraeten, Inge and Zhang, Yuzhou and Friml, Jiří},
  issn         = {1532-2548},
  journal      = {Plant Physiology},
  number       = {5},
  pages        = {37--40},
  publisher    = {American Society of Plant Biologists},
  title        = {{SCF TIR1/AFB auxin signaling for bending termination during shoot gravitropism}},
  doi          = {10.1104/pp.20.00212},
  volume       = {183},
  year         = {2020},
}

