The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Armadillo is required for adherens junction assembly, cell polarity, and morphogenesis during Drosophila embryogenesis.
Open accessAbstract
Morphological and biochemical analyses have identified a set of proteins which together form a structure known as the adherens junction. Elegant experiments in tissue culture support the idea that adherens junctions play a key role in cell-cell adhesion and in organizing cells into epithelia. During normal embryonic development, cells quickly organize epithelia; these epithelial cells participate in many of the key morphogenetic movements of gastrulation. This prompted the hypothesis that adherens junctions ought to be critical for normal embryonic development. Drosophila Armadillo, the homologue of vertebrate beta-catenin, is a core component of the adherens junction protein complex and has been hypothesized to be essential for adherens junction function in vivo. We have used an intermediate mutant allele of armadillo, armadilloXP33, to test these hypotheses in Drosophila embryos. Adherens junctions cannot assemble in the absence of Armadillo, leading to dramatic defects in cell-cell adhesion. The epithelial cells of the embryo lose adhesion to each other, round up, and apparently become mesenchymal. Mutant cells also lose their normal cell polarity. These disruptions in the integrity of epithelia block the appropriate morphogenetic movements of gastrulation. These results provide the first demonstration of the effect of loss of adherens junctions on Drosophila embryonic development.
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“Indeed, experiments in Drosophila have shown that mutations in junctional proteins not only affect junction formation but also disturb epithelial polarity, whereas polarity mutants have a profound effect on junction formation as well (Cox et al, 1996;Muller and Wieschaus, 1996;Tanentzapf et al, 2000).”
From E‐cadherin is essential for in vivo epidermal barrier function by regulating tight junctions (2005) · cites this paper as Cox et al, 1996
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Citations
Cites
Müller, H. A., & Wieschaus, E. (1996) · The Journal of cell biology · doi:10.1083/jcb.134.1.149 · Cited by 384
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Items 201–271 of 271
Actomyosin contractility modulates Wnt signaling through adherens junction stability
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BackgroundSomorjai, I., & Martínez-Arias, A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002893 · Cited by 13
“Few data exist in animal models on the subcellular distribution of Armadillo/b-catenin and E-Cadherin in the context of their function, with notable exceptions [28,35,44–48].”
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“This is probably due to the requirement of Arm in cell adhesion or viability in addition to Wg signaling (Peifer et al., 1993; Cox et al., 1996; Wehrli and Tomlinson, 1998).”
BackgroundTwo Themes on the Assembly of the Drosophila Eye
Bao, S. (2010) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385044-7.00004-7 · Cited by 11
“Loss of Armadillo, the fly ortholog of b-catenin, leads to disruption of polarity of the actin cytoskeleton (Cox et al., 1996).”
BackgroundDeltex interacts with Eiger and consequently influences the cell death in Drosophila melanogaster.
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“As in mammalian epithelia [15,16], the main functional components of this complex in Drosophila are the transmembrane protein Ecadherin, a calcium-dependent trans-membrane adhesion molecule, and the catenins (Armadillo and α-catenin) that link E-cadherin to the actin cytoskeleton at the cytoplasmic side [17-22].”
BackgroundDally-like protein sequesters multiple Wnt ligands in the Drosophila germarium
Waghmare, I., Wang, X., & Page-McCaw, A. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.05.004 · Cited by 11
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Johnson, T. K., Moore, K. A., Whisstock, J., & Warr, C. G. (2017) · Genetics · doi:10.1534/genetics.117.200576 · Cited by 10
“Therefore, we assessed constriction at the onset of ventral furrow formation by staining embryos for b-catenin, an integral intracellular component of the AJ (Cox et al. 1996).”
MethodFan, S.-S. (2004) · Journal of Biomedical Sciences · doi:10.1007/bf02254441 · Cited by 10
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“For example, cadherins negatively regulate β-catenin by competing for interaction with Lef/Tcf factors and perhaps, by tethering β-catenin to the cell plasma membrane away from the nucleus (Cox et al., 1996; Fagotto et al., 1996; Heasman et al., 1994; Orsulic et al., 1999; Sanson et al., 1996).”
BackgroundNaturale, V. F., Pickett, M., & Feldman, J. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.07.008 · Cited by 8
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“The initial analysis of Ecad, Arm, and α -catenin fit this simple model: loss of each totally disrupted cell adhesion, and thus completely halted morphogenesis (Cox et al. , 1996; Müller and Wieschaus, 1996; Tepass et al. , 1996; Sarpal et al. , 2012).”
Self-citationPlanar Cell Polarity and E-Cadherin in Tissue-Scale Shape Changes in Drosophila Embryos
Kong, D., & Grosshans, J. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.619958 · Cited by 8
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Ammeri, R. W., Hidri, Y., & Hassen, A. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.93714 · Cited by 12
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Drosophila renal stem cells enhance fitness by delayed remodeling of adult Malpighian tubules
Wang, C., & Spradling, A. C. (2022) · Science Advances · doi:10.1126/sciadv.abn7436 · Cited by 3
“…septate junctions (SJs) and adherens junction (AJ) are crucial for epithelial barrier function and cell adhesion in invertebrates, we examined the expression and localization of the conserved SJ protein Coracle and the AJ core component Armadillo in lower tubules following regeneration ( 10 , 11 ).”
Dynamic Expression Profiles of β-Catenin during Murine Cardiac Valve Development
Guo, L., Glover, J. S., Risner, A., Wang, C. E., Fulmer, D. B., Moore, K. S., Gensemer, C., Rumph, M. K., Moore, R. A., Beck, T. C., et al. (2020) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd7030031 · Cited by 6
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Nuclear β-catenin: molecular regulation, challenges and therapeutic opportunities
Xie, B., Cao, Y., Li, W., Chen, R., Zhou, Q., & Xie, X. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02600-6 · Cited by 4
“Consistent with this view, low concentrations drive Drosophila β-catenin to adherens junctions, implying a stronger binding affinity for cadherin [178].”
β-Catenin immunocytochemical reactivity in cervicovaginal smears during regular menstrual cycles
Donmez, H. (2020) · Asian Biomedicine · doi:10.1515/abm-2020-0027 · Cited by 5
ESSAYS ON SCIENCE AND SOCIETY: Making a Bigger Brain by Regulating Cell Cycle Exit
Chenn, A. (2002) · Science · doi:10.1126/science.1079328 · Cited by 5
A Simple Method to Assess Abundance of the β-Catenin Signaling Pool in Cells
Flozak, A. S., Lam, A. P., & Gottardi, C. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6393-5_6 · Cited by 5
Apical transport of Crumbs maintains epithelial cell polarityPreprint
Aguilar-Aragon, M., Fletcher, G., & Thompson, B. (2019) · bioRxiv · doi:10.1101/592311 · Cited by 4
“5 The actin cytoskeleton is organized by the Rho GTPase and adherens junctions (Cox et al., 1996; Fox et al., 2005; Homem and Peifer, 2008; Muller and Wieschaus, 1996; Peifer et al., 1993) which are ultimately positioned between the core apical and basolateral polarity determinants.”
BackgroundStructural Aspects of Adherens Junctions and Desmosomes
Choi, H., & Weis, W. I. (2004) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-68170-0_2 · Cited by 4
“Similarly, the C-terminal region does not appear to be required for adhesive interactions, and there are no known adherens junction proteins that bind in this region: Drosophila embryos containing a C-terminally deleted b-catenin show normal adherens junctions but are defective in Wnt signaling ( Cox et al. 1996 ).”
BackgroundAkarsu, G., MacCharles, K. R., Wong, K. K., Richman, J. M., & Verheyen, E. (2024) · bioRxiv · doi:10.1002/dvdy.70056 · Cited by 3
Ru, H., Finet, C., & Monteiro, A. (2024) · bioRxiv · doi:10.1101/2024.09.12.612608 · Cited by 3
E-cadherin/HMR-1 and PAR-3 break symmetry at stable cell contacts in a developing epitheliumPreprint
Naturale, V. F., Pickett, M., & Feldman, J. (2022) · bioRxiv · doi:10.1101/2022.08.10.503536 · Cited by 3
“However, specific symmetry breaking functions for E-cadherin have often been obscured by its essential role in cell/cell adhesion (Cox et al., 1996; Johnson et al., 1986; Peifer et al., 1993; Shirayoshi et al., 1983; Stephenson et al., 2010).”
BackgroundArm-Gal4 inheritance influences development and lifespan in Drosophila melanogaster.
Slade, F. A., & Staveley, B. E. (2015) · Genetics and Molecular Research · doi:10.4238/2015.october.19.22 · Cited by 3
“Arm is multifunctional and is involved in intracellular signaling, cytoskeletal regulation, and cell adhesion during embryogenesis (Peifer et al., 1993; Cox et al., 1996; Sanson et al., 1996).”
BackgroundCell Adhesion in the Assembly of the Drosophila Eye
Bao, S.-J. (2014) · Journal of neurogenetics · doi:10.3109/01677063.2014.907799 · Cited by 3
“Armadillo, the fly b-catenin, leads to disruption of polarity of the actin cytoskeleton (Cox et al., 1996).”
BackgroundWhen domestiques rebel: kinesins, cadherins and neuronal proliferation
Gottardi, C. J., den Elzen, N. R., & Yap, A. S. (2005) · Nature Cell Biology · doi:10.1038/ncb0505-445 · Cited by 3
Alteration of Cytoskeletal Proteins Leads to Retinal Degeneration in Drosophila
Sahu, S., & Mishra, M. (2024) · Cytoskeleton · doi:10.1002/cm.21955 · Cited by 2
“During morphogenesis, retinal cells are interconnected by AJs, which consist of core components such as N-cadherin (N-cad), actin, and armadillo (Arm) (Cox, Kirkpatrick, and Peifer 1996; Tepass and Harris 2007).”
Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
Camuglia, J., Chanet, S., & Martin, A. C. (2022) · bioRxiv · doi:10.1101/2022.01.07.475359 · Cited by 2
“Epithelia are tissues composed of cells that are organized in a sheet and held 44 together by junctions, which maintain the integrity of the tissue as well as the apical-basal polarity 45 of cells (Choi et al., 2013; Classen et al., 2005; Cox et al., 1996; Gumbiner, 2005; Harris and 46 Peifer 2005; Tepass, 1997; Wang…”
The function of α-Catenin mechanosensing in tissue morphogenesis
Sheppard, L., & Tepass, U. (2021) · bioRxiv · doi:10.1101/2021.09.08.459511 · Cited by 2
“During cellularization, Cno recruitment is unaffected by the loss of Arm, and instead requires the small GTPase Rap1 (Sawyer et al., 2009).”
BackgroundInfluentialBonello, T. T., & Peifer, M. (2019) · bioRxiv · doi:10.1101/654509 · Cited by 2
“AJ proteins are not essential for syncytial divisions (Grevengoed et al., 2003), but in their absence cell adhesion and polarity are lost when gastrulation begins (Cox et al., 1996; Müller and Wieschaus, 1996; Sarpal et al., 2012; Tepass et al., 1996).”
BackgroundSelf-citationDenis, H. (1997) · médecine/sciences · doi:10.4267/10608/591 · Cited by 2
“Chez la drosophile, c’est apparemment une constriction apicale qui contraint les cellules à s’invaginer (figure 6) [32, 33].”
BackgroundBogdanova, E., Beresneva, O., Zubina, I., Ivanova, G., Parastaeva, M., Galkina, O., & Dobronravov, V. (2020) · Nephrology (Saint-Petersburg) · doi:10.36485/1561-6274-2020-24-6-85-92 · Cited by 1
Cadherin Regulation of Adhesive Interactions
Ranscht, B. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374145-5.00242-4 · Cited by 1
Ganguly, A., & Ip, Y. (2005) · doi:10.1007/0-387-28671-3_7 · Cited by 1
Cruz, E. R., Marishta, A., Bao, G., Johnson, A. N. T., Keber, F. C., Pujari, V., Ivanov, D., Neinast, M. D., Kirschner, M. W., Rabinowitz, J. D., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.28.754234
“Armadillo, the Drosophila -catenin homolog, degraded from the inherited pool with a half-life of 4.6 hours while its total abundance rose in the control channels, consistent with its roles in Wingless signaling and adherens-junction assembly 84,85 .”
InfluentialEpidermal and ECM Damage Following Pinch Injury Restricts Dendrite Regeneration in Drosophila
Brantley, M. A., Pandiyan, A., Danh, A. C., Prange, S. E., Rimicci, D. S., & Thompson-Peer, K. L. (2026) · bioRxiv · doi:10.64898/2026.07.15.738747
“To visualize the epidermis, we used a GFP-tagged version of Armadillo, the fly homolog of beta-catenin and an adherens-junction marker (Cox et al., 1996).”
Clark, S. E., Morris, S. C., Dordor, J. B., Amo, L. S., Wiltshire, R., Encarnacion, T., Bischoff, M. C., & Peifer, M. (2026) · bioRxiv · doi:10.64898/2026.05.22.727264
Self-citationMcCabe, M., Dunkel, M., Negahdar, A., Yoshinaga-Sakurai, K., & Jia, D. (2026) · Scientific Reports · doi:10.1038/s41598-025-33929-0
“Arm plays an essential role in the assembly of apicolateral cell adherens junctions, and is therefore normally apicolaterally localized 24,25 .”
Gαq controls organ size and developmental timing in Drosophila
Unger, M. F., Velagala, V. K. N., Soundarrajan, D. K., Gazzo, D., Kumar, N., Flores, M., Liu, J., Li, J., & Zartman, J. J. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02449-9
“Cell adhesion is crucial in morphogenesis and when disrupted, results in metastatic cancer [78].”
Sabbagh, S., & Harris, T. J. C. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2024.10.001
Carvalho, C. A., Tame, M., & Johnston, D. S. (2024) · bioRxiv · doi:10.1101/2024.03.22.586295
“However, in embryos derived from germline clones of strong β-catenin mutants ( arm ) that also lack zygotic β-catenin, embryonic tissues lose their epithelial characteristics at gastrulation, producing unpolarised mesenchymal cells (Cox et al., 1996).”
BackgroundAntel, M., Norris, R., & Inaba, M. (2022) · bioRxiv · doi:10.1101/2022.11.22.517537
“E-Cadherin is involved in multiple biological processes, including establishing and maintaining cell adhesion [10, 11], cell migration [12] and spindle orientation [13].”
BackgroundDonmez, H., & Akan, H. S. (2022) · Hacettepe Journal of Biology and Chemistry · doi:10.15671/hjbc.1001427
Donmez, H., Çelik, H., Kaykı, G., Tanaçan, A., Çağan, M., Yiğit, Ş., Yurdakok, M., Cakar, A., & Beksaç, M. (2021) · American Journal of Perinatology · doi:10.1055/s-0041-1740348
“16 Apoptosis is a genetically controlled programmed cell death that plays an important role in many physiological and pathological events.”
BackgroundInfluentialThe RhoGEF Cysts couples apical polarity proteins to Rho and myosin activity at adherens junctions
Silver, J. T., Wirtz-Peitz, F., Simões, S., Pellikka, M., Yan, D., Binari, R., Nishimura, T., Li, Y., Harris, T., Perrimon, N., et al. (2019) · bioRxiv · doi:10.1101/617134
“A crb-like phenotype has been documented for only a small number of genes that encode apical polarity proteins such as crb and stardust (sdt), or genes encoding AJ proteins such as bazooka (baz), shotgun (encoding DEcad) or armadillo (arm; Drosophila β-catenin) (Tepass et al., 1990, Tepass and Knust, 1990; 1993; Tepas…”
BackgroundA fence function for adherens junctions in epithelial cell polarityPreprint
Aguilar-Aragon, M., Tournier, A., & Thompson, B. (2019) · bioRxiv · doi:10.1101/605808
“While adherens junctions are known to be essential for epithelial cell shape [29-32], their exact role in polarisation of epithelial polarity determinants is still unclear.”
BackgroundCharacterisation of l(3)tb as a novel tumour suppressor allele of DCP2 in Drosophila melanogaster
Mishra, R., Kunar, R., Mandal, L., Alone, D. P., Chandrasekharan, S., Tiwari, A., Mukherjee, A., Tapadia, M. G., & Roy, J. K. (2019) · bioRxiv · doi:10.1101/574707
“…and Dlg and the simultaneous loss of Elav in the later larval stages in the l(3)tb mutants may be due to disassembly of the adherens junctions (Cox et al, 1996) thereby affecting cell-cell adhesion between glial and neuronal bodies in the brain and in the over-proliferative cells of the wing…”
BackgroundRole of crumbs and bazooka in the organization and distribution of DE-cadherin in Drosophila embryo
Aksenova, V. (2017) · theses.fr (ABES) · doi:10.70675/5067594bzfce9z45acz9961zbfc33be662bd
Etude de la fonction de Patj dans la régulation de la polarité épithéliale.
Pénalva, C. (2014) · theses.fr (ABES) · doi:10.70675/9974aeb2z5e64z46d6zaa51z1908380bf779
“Dès l’apparition du sillon les AJ se forment au niveau de la protrusion apicale de celui-ci (Fig.12), (Cox et al., 1996; Harris and Peifer, 2004; Harris and Peifer, 2005; Müller and Wieschaus, 1996; Tepass and Hartenstein, 1994).”
BackgroundFan, S.-S. (2004) · Journal of Biomedical Sciences · doi:10.1159/000077105
β-Catenin Regulation of Adult Skeletal Muscle Plasticity
Wen, Y. (2018) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2018.030
“16 component of the adherens junction protein complex [45].”
BackgroundSpracklen, A. J. (2014) · doi:10.17077/etd.wids38sf
“, 2013) or β-Catenin (Peifer et al., 1993; Cox et al., 1996; Oda et al., 1997; White et al., 1998) results in numerous defects in oogenesis including aberrant follicle cell packaging of germline cysts, oocyte mispositioning, nurse cell cortical actin breakdown, disrupted cytoplasmic actin filament bundle formation, an…”
BackgroundInfluential
Metadata
- Authors
- Cox, R. T., Kirkpatrick, C., & Peifer, M.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1996-07-01
- Volume
- 134
- Issue
- 1
- Pages
- 133-148
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2120919
- OpenAlex
- W2030945799
- Cited by
- 300
- References
- 58
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4 · 2023: 2 · 2022: 7 · 2021: 6 · 2020: 8 · 2019: 9 · 2018: 6 · 2017: 7 · 2016: 4 · 2015: 3 · 2014: 3 · 2013: 10 · 2012: 7
- FWCI
- 7.46
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM007092, 5T32 GM-07092)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Keywords
- armadillos, β-catenin, cell-cell adhesion, epithelial morphogenesis, cell polarity, gastrulation, Drosophila embryogenesis, mesenchymal transition, epithelial barrier integrity
- MeSH terms
- Actins, Animals, Cell Adhesion, Cytoskeletal Proteins, DNA Mutational Analysis, Drosophila melanogaster, Epithelial Cells, Gastrula, Intercellular Junctions, Membrane Proteins, Actin Cytoskeleton, Microscopy, Electron, Scanning, Morphogenesis, Oogenesis, Proteins, Transcription Factors, Trans-Activators, Cell Adhesion Molecules, Cadherins, Cell Polarity, Drosophila Proteins, alpha Catenin, Armadillo Domain Proteins
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