Arp2/3 Complex Is Required for Auxin-Driven Cell Expansion Through Regulation of Auxin Transporter Homeostasis
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
32425966
PubMed Central
PMC7212389
DOI
10.3389/fpls.2020.00486
Knihovny.cz E-zdroje
- Klíčová slova
- Arp2/3 complex, actin, auxin, cell expansion, cytoskeleton,
- Publikační typ
- časopisecké články MeSH
The Arp2/3 complex is an actin nucleator shown to be required throughout plant morphogenesis, contributing to processes such as cell expansion, tissue differentiation or cell wall assembly. A recent publication demonstrated that plants lacking functional Arp2/3 complex also present defects in auxin distribution and transport. This work shows that Arp2/3 complex subunits are predominantly expressed in the provasculature, although other plant tissues also show promoter activity (e.g., cotyledons, apical meristems, or root tip). Moreover, auxin can trigger subunit expression, indicating a role of this phytohormone in mediating the complex activity. Further investigation of the functional interaction between Arp2/3 complex and auxin signaling also reveals their cooperation in determining pavement cell shape, presumably through the role of Arp2/3 complex in the correct auxin carrier trafficking. Young seedlings of arpc5 mutants show increased auxin-triggered proteasomal degradation of DII-VENUS and altered PIN3 distribution, with higher levels of the protein in the vacuole. Closer observation of vacuolar morphology revealed the presence of a more fragmented vacuolar compartment when Arp2/3 function is abolished, hinting a generalized role of Arp2/3 complex in endomembrane function and protein trafficking.
Department of Experimental Plant Biology Faculty of Science Charles University Prague Czechia
Institute of Experimental Botany Czech Academy of Sciences Prague Czechia
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Abas L., Benjamins R., Malenica N., Paciorek T., Wiśniewska J., Wirniewska J., et al. (2006). Intracellular trafficking and proteolysis of the Arabidopsis auxin-efflux facilitator PIN2 are involved in root gravitropism. PubMed DOI
Aloni R., Schwalm K., Langhans M., Ullrich C. I. (2003). Gradual shifts in sites of free-auxin production during leaf-primordium development and their role in vascular differentiation and leaf morphogenesis in PubMed DOI
Armour W. J., Barton D. A., Law A. M. K., Overall R. L. (2015). Differential growth in periclinal and anticlinal walls during lobe formation in Arabidopsis cotyledon pavement cells. PubMed DOI PMC
Bachmair A., Zazimalova E., Petrasek J., Luschnig C., Korbei B., Leitner J., et al. (2012). Lysine PubMed DOI PMC
Bao C., Wang J., Zhang R., Zhang B., Zhang H., Zhou Y., et al. (2012). Arabidopsis VILLIN2 and VILLIN3 act redundantly in sclerenchyma development via bundling of actin filaments. PubMed DOI
Baster P., Robert S., Kleine-Vehn J., Vanneste S., Kania U., Grunewald W., et al. (2013). SCFTIR1/AFB-auxin signalling regulates PIN vacuolar trafficking and auxin fluxes during root gravitropism. PubMed DOI PMC
Belteton S. A., Sawchuk M. G., Donohoe B. S., Scarpella E., Szymanski D. B. (2018). Reassessing the roles of PIN proteins and anticlinal microtubules during pavement cell morphogenesis. PubMed DOI PMC
Braybrook S. A., Peaucelle A. (2013). Mechano-chemical aspects of organ formation in PubMed DOI PMC
Brembu T., Winge P., Seem M., Bones A. M. (2004). NAPP and PIRP encode subunits of a putative wave regulatory protein complex involved in plant cell morphogenesis. PubMed DOI PMC
Brunoud G., Wells D. M., Oliva M., Larrieu A., Mirabet V., Burrow A. H., et al. (2012). A novel sensor to map auxin response and distribution at high spatio-temporal resolution. PubMed DOI
Cheng Y., Dai X., Zhao Y. (2007). Auxin synthesized by the YUCCA Flavin Monooxygenases is essential for embryogenesis and leaf formation in PubMed DOI PMC
Datia R. S. S., Hammerlindl J. K., Panchuk B., Pelcher L. E., Keller W. (1992). Modified binary plant transformation vectors with the wild-type gene encoding NPTII. PubMed DOI
Deeks M. J., Hussey P. J. (2003). Arp2/3 and ‘the shape of things to come’. PubMed DOI
Deeks M. J., Kaloriti D., Davies B., Malhó R., Hussey P. J. (2004). Arabidopsis NAP1 is essential for Arp2/3-dependent trichome morphogenesis. PubMed DOI
Djakovic S., Dyachok J., Burke M., Frank M. J., Smith L. G. (2006). BRICK1/HSPC300 functions with SCAR and the ARP2/3 complex to regulate epidermal cell shape in PubMed DOI
Dobrev P. I., Vankova R. (2012). Quantification of abscisic Acid, cytokinin, and auxin content in salt-stressed plant tissues. PubMed DOI
Dyachok J., Shao M. R., Vaughn K., Bowling A., Facette M., Djakovic S., et al. (2008). Plasma membrane-associated SCAR complex subunits promote cortical F-actin accumulation and normal growth characteristics in PubMed DOI
Dyachok J., Zhu L., Liao F., He J., Huq E., Blancaflor E. B. (2011). SCAR mediates light-induced root elongation in PubMed DOI PMC
El-Assal S. E. D., Le J., Basu D., Mallery E. L., Szymanski D. B. (2004). Distorted2 encodes an ARPC2 subunit of the putative PubMed DOI
Falconer M. M., Seagull R. W. (1985). Xylogenesis in tissue culture: Taxol effects on microtubule reorientation and lateral association in differentiating cells. DOI
Feraru E., Feraru M. I., Kleine-Vehn J., Martiničre A., Mouille G., Vanneste S., et al. (2011). PIN polarity maintenance by the cell wall in Arabidopsis. PubMed DOI
Friml J., Wiśniewska J., Benková E., Mendgen K., Palme K. (2002). Lateral relocation of auxin efflux regulator PIN3 mediates tropism in PubMed DOI
Gallavotti A. (2013). The role of auxin in shaping shoot architecture. PubMed DOI
Gälweiler L., Guan C., Müller A., Wisman E., Mendgen K., Yephremov A., et al. (1998). Regulation of polar auxin transport by AtPIN1 in Arabidopsis vascular tissue. PubMed DOI
Ganguly A., Park M., Kesawat M. S., Cho H.-T. (2014). Functional analysis of the hydrophilic loop in intracellular trafficking of Arabidopsis PIN-FORMED proteins. PubMed DOI PMC
Gao Y., Zhang Y., Zhang D., Dai X., Estelle M., Zhao Y. (2015). Auxin binding protein 1 (ABP1) is not required for either auxin signaling or Arabidopsis development. PubMed DOI PMC
Gardiner J. C., Taylor N. G., Turner S. R. (2003). Control of cellulose synthase complex localization in developing xylem. PubMed DOI PMC
Geldner N., Friml J., Stierhof Y. D., Jürgens G., Palme K. (2001). Auxin transport inhibitors block PIN1 cycling and vesicle trafficking. PubMed DOI
Hepler P. K., Fosket D. E. (1971). The role of microtubules in vessel member differentiation inColeus. DOI
Hou G., Mohamalawari D. R., Blancaflor E. B. (2003). Enhanced gravitropism of roots with a disrupted cap. PubMed DOI PMC
Jiang K., Sorefan K., Deeks M. J., Bevan M. W., Hussey P. J., Hetherington A. M. (2012). The ARP2/3 complex mediates guard cell actin reorganization and stomatal movement in PubMed DOI PMC
Klahre U., Chua N. H. (1999). The Arabidopsis ACTIN-RELATED PROTEIN 2 (AtARP2) promoter directs expression in xylem precursor cells and pollen. PubMed DOI
Kleine-Vehn J., Leitner J., Zwiewka M., Sauer M., Abas L., Luschnig C., et al. (2008a). Differential degradation of PIN2 auxin efflux carrier by retromer-dependent vacuolar targeting. PubMed DOI PMC
Kleine-Vehn J., Wabnik K., Martiničre A., Łangowski Ł., Willig K., Naramoto S., et al. (2011). Recycling, clustering, and endocytosis jointly maintain PIN auxin carrier polarity at the plasma membrane. PubMed DOI PMC
Kleine-Vehn J., Wiśniewska J., Brewer P. B., Friml J., Dhonukshe P., Łangowski Ł. (2008b). Cellular and molecular requirements for polar PIN targeting and transcytosis in plants. PubMed DOI
Koltzscher M., Neumann C., Kö S., Gerke V. (2003). Ca PubMed DOI PMC
Kramer E. M., Ackelsberg E. M. (2016). Do vacuoles obscure the evidence for auxin homeostasis? PubMed DOI
Kremers G.-J., Davidson M. W., Sell B. R., Baird M. A., Lavagnino Z., Ustione A., et al. (2016). Quantitative assessment of fluorescent proteins. PubMed DOI PMC
Krüger F., Schumacher K. (2018). Pumping up the volume - vacuole biogenesis in PubMed DOI
Lacek J., Retzer K., Luschnig C., Zažímalová E. (2017). “Polar auxin transport,” in DOI
Lanza M., Garcia-Ponce B., Castrillo G., Catarecha P., Sauer M., Rodriguez-Serrano M., et al. (2012). Role of actin cytoskeleton in brassinosteroid signaling and in its integration with the auxin response in plants. PubMed DOI
Laxmi A., Pan J., Morsy M., Chen R. (2008). Light plays an essential role in intracellular distribution of auxin efflux carrier PIN2 in PubMed DOI PMC
Le J., El-Assal S. E.-D., Basu D., Saad M. E., Szymanski D. B. (2003). Requirements for PubMed DOI
Le J., Liu X.-G., Yang K.-Z., Chen X.-L., Zou J.-J., Wang H.-Z., et al. (2014). Auxin transport and activity regulate stomatal patterning and development. PubMed DOI
Le J., Mallery E. L., Zhang C., Brankle S., Szymanski D. B. (2006). PubMed DOI
Li H., Lin D., Dhonukshe P., Nagawa S., Chen D., Friml J., et al. (2011). Phosphorylation switch modulates the interdigitated pattern of PIN1 localization and cell expansion in PubMed DOI PMC
Li L.-J., Ren F., Gao X.-Q., Wei P.-C., Wang X.-C. (2013). The reorganization of actin filaments is required for vacuolar fusion of guard cells during stomatal opening in PubMed DOI
Li S., Blanchoin L., Yang Z., Lord E. M. (2003). The putative Arabidopsis arp2/3 complex controls leaf cell morphogenesis. PubMed DOI PMC
Löfke C., Dünser K., Scheuring D., Kleine-Vehn J. (2015). Auxin regulates SNARE-dependent vacuolar morphology restricting cell size. PubMed DOI PMC
Mao G., Buschmann H., Doonan J. H., Lloyd C. W. (2006). The role of MAP65-1 in microtubule bundling during Zinnia tracheary element formation. PubMed DOI
Mathur J., Mathur N., Kernebeck B., Hülskamp M. (2003a). Mutations in actin-related proteins 2 and 3 affect cell shape development in Arabidopsis. PubMed DOI PMC
Mathur J., Mathur N., Kirik V., Kernebeck B., Srinivas B. P., Hülskamp M. (2003b). Arabidopsis CROOKED encodes for the smallest subunit of the ARP2/3 complex and controls cell shape by region specific fine F-actin formation. PubMed DOI
Mathur J., Spielhofer P., Kost B., Chua N. (1999). The actin cytoskeleton is required to elaborate and maintain spatial patterning during trichome cell morphogenesis in PubMed
Nagawa S., Xu T., Lin D., Dhonukshe P., Zhang X., Friml J., et al. (2012). ROP GTPase-dependent actin microfilaments promote PIN1 polarization by localized inhibition of clathrin-dependent endocytosis. PubMed DOI PMC
Nakayama N., Smith R. S., Mandel T., Robinson S., Kimura S., Boudaoud A., et al. (2012). Mechanical regulation of auxin-mediated growth. PubMed DOI
Narusaka M., Shiraishi T., Iwabuchi M., Narusaka Y. (2010). The floral inoculating protocol: a simplified DOI
Nelson B. K., Cai X., Nebenführ A. (2007). A multicolored set of PubMed DOI
Oda Y., Fukuda H. (2012). Initiation of cell wall pattern by a Rho- and microtubule-driven symmetry breaking. PubMed DOI
Oda Y., Fukuda H. (2013). Rho of Plant GTPase signaling regulates the behavior of PubMed DOI PMC
Oda Y., Iida Y., Kondo Y., Fukuda H. (2010). Wood cell-wall structure requires local 2D-microtubule disassembly by a novel plasma membrane-anchored protein. PubMed DOI
Pénčík A., Simonovik B., Petersson S. V., Henyková E., Simon S., Greenham K., et al. (2013). Regulation of auxin homeostasis and gradients in PubMed DOI PMC
Pesquet E., Korolev A. V., Calder G., Lloyd C. W. (2010). The microtubule-associated protein AtMAP70-5 regulates secondary wall patterning in PubMed DOI
Rahman A., Bannigan A., Sulaman W., Pechter P., Blancaflor E. B., Baskin T. I. (2007). Auxin, actin and growth of the PubMed DOI
Ramakers C., Ruijter J. M., Lekanne Deprez R. H., Moorman A. F. M. (2003). Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data. PubMed DOI
Saedler R., Zimmermann I., Mutondo M., Hülskamp M. (2004). The PubMed DOI
Sahi V. P., Cifrová P., Garciá-González J., Kotannal Baby I., Mouillé G., Gineau E., et al. (2018). PubMed DOI PMC
Saini S., Sharma I., Kaur N., Pati P. K. (2013). Auxin: a master regulator in plant root development. PubMed DOI
Salanenka Y., Verstraeten I., Löfke C., Tabata K., Naramoto S., Glanc M., et al. (2018). Gibberellin DELLA signaling targets the retromer complex to redirect protein trafficking to the plasma membrane. PubMed DOI PMC
Sasaki T., Fukuda H., Oda Y. (2017). CORTICAL MICROTUBULE DISORDERING1 is required for secondary cell wall patterning in xylem vessels. PubMed DOI PMC
Schindelin J., Arganda-Carreras I., Frise E., Kaynig V., Longair M., Pietzsch T., et al. (2012). Fiji: an open-source platform for biological-image analysis. PubMed DOI PMC
Schwab B., Mathur J., Saedler R., Schwarz H., Frey B., Scheidegger C., et al. (2003). Regulation of cell expansion by the DISTORTED genes in PubMed DOI
Shimada T., Takagi J., Ichino T., Shirakawa M., Hara-Nishimura I. (2018). Plant vacuoles. PubMed DOI
Shinoda H., Shannon M., Nagai T. (2018). Fluorescent proteins for investigating biological events in acidic environments. PubMed DOI PMC
Shirakawa M., Ueda H., Shimada T., Nishiyama C., Hara-Nishimura I. (2009). Vacuolar SNAREs function in the formation of the leaf vascular network by regulating auxin distribution. PubMed DOI
Sugiyama Y., Nagashima Y., Wakazaki M., Sato M., Toyooka K., Fukuda H., et al. (2019). A Rho-actin signaling pathway shapes cell wall boundaries in Arabidopsis xylem vessels. PubMed DOI PMC
Teale W. D., Paponov I. A., Palme K. (2006). Auxin in action: signalling, transport and the control of plant growth and development. PubMed DOI
Viotti C., Krüger F., Krebs M., Neubert C., Fink F., Lupanga U., et al. (2013). The endoplasmic reticulum is the main membrane source for biogenesis of the lytic vacuole in PubMed DOI PMC
Vukašinović N., Oda Y., Pejchar P., Synek L., Pečenková T., Rawat A., et al. (2017). Microtubule-dependent targeting of the exocyst complex is necessary for xylem development in Arabidopsis. PubMed DOI
Wang P., Richardson C., Hawes C., Hussey P. J. (2016). PubMed DOI
Welch M. D., DePace A. H., Verma S., Iwamatsu A., Mitchison T. J. (1997). The human Arp2/3 complex is composed of evolutionarily conserved subunits and is localized to cellular regions of dynamic actin filament assembly. PubMed DOI PMC
Wu T.-C., Belteton S. A., Pack J., Szymanski D. B., Umulis D. M. (2016). LobeFinder: a convex hull-based method for quantitative boundary analyses of lobed plant cells. PubMed DOI PMC
Xu T., Dai N., Chen J., Nagawa S., Cao M., Li H., et al. (2014). Cell surface ABP1-TMK auxin-sensing complex activates ROP GTPase signaling. PubMed DOI PMC
Xu T., Wen M., Nagawa S., Fu Y., Chen J.-G., Wu M.-J., et al. (2010). Cell surface- and rho GTPase-based auxin signaling controls cellular interdigitation in PubMed DOI PMC
Yamamoto K., Kiss J. Z. (2002). Disruption of the actin cytoskeleton results in the promotion of gravitropism in inflorescence stems and hypocotyls of Arabidopsis. PubMed DOI PMC
Yanagisawa M., Desyatova A. S., Belteton S. A., Mallery E. L., Turner J. A., Szymanski D. B. (2015). Patterning mechanisms of cytoskeletal and cell wall systems during leaf trichome morphogenesis. PubMed DOI
Žádníková P., Petrasek J., Marhavy P., Raz V., Vandenbussche F., Ding Z., et al. (2010). Role of PIN-mediated auxin efflux in apical hook development of PubMed DOI
Zhang C., Halsey L. E., Szymanski D. B. (2011). The development and geometry of shape change in PubMed DOI PMC
Zhang C., Hicks G. R., Raikhel N. V. (2014). Plant vacuole morphology and vacuolar trafficking. PubMed DOI PMC
Zhang C., Mallery E. L., Szymanski D. B. (2013). ARP2/3 localization in Arabidopsis leaf pavement cells: a diversity of intracellular pools and cytoskeletal interactions. PubMed DOI PMC
Zhao Y., Christensen S. K., Fankhauser C., Cashman J. R., Cohen J. D., Weigel D., et al. (2001). A role for flavin monooxygenase-like enzymes in auxin biosynthesis. PubMed DOI
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