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  1. Article ; Online: Interplay between axonal Wnt5-Vang and dendritic Wnt5-Drl/Ryk signaling controls glomerular patterning in the Drosophila antennal lobe.

    Hing, Huey / Reger, Noah / Snyder, Jennifer / Fradkin, Lee G

    PLoS genetics

    2020  Volume 16, Issue 5, Page(s) e1008767

    Abstract: Despite the importance of dendritic targeting in neural circuit assembly, the mechanisms by which it is controlled still remain incompletely understood. We previously showed that in the developing Drosophila antennal lobe, the Wnt5 protein forms a ... ...

    Abstract Despite the importance of dendritic targeting in neural circuit assembly, the mechanisms by which it is controlled still remain incompletely understood. We previously showed that in the developing Drosophila antennal lobe, the Wnt5 protein forms a gradient that directs the ~45˚ rotation of a cluster of projection neuron (PN) dendrites, including the adjacent DA1 and VA1d dendrites. We report here that the Van Gogh (Vang) transmembrane planar cell polarity (PCP) protein is required for the rotation of the DA1/VA1d dendritic pair. Cell type-specific rescue and mosaic analyses showed that Vang functions in the olfactory receptor neurons (ORNs), suggesting a codependence of ORN axonal and PN dendritic targeting. Loss of Vang suppressed the repulsion of the VA1d dendrites by Wnt5, indicating that Wnt5 signals through Vang to direct the rotation of the DA1 and VA1d glomeruli. We observed that the Derailed (Drl)/Ryk atypical receptor tyrosine kinase is also required for the rotation of the DA1/VA1d dendritic pair. Antibody staining showed that Drl/Ryk is much more highly expressed by the DA1 dendrites than the adjacent VA1d dendrites. Mosaic and epistatic analyses showed that Drl/Ryk specifically functions in the DA1 dendrites in which it antagonizes the Wnt5-Vang repulsion and mediates the migration of the DA1 glomerulus towards Wnt5. Thus, the nascent DA1 and VA1d glomeruli appear to exhibit Drl/Ryk-dependent biphasic responses to Wnt5. Our work shows that the final patterning of the fly olfactory map is the result of an interplay between ORN axons and PN dendrites, wherein converging pre- and postsynaptic processes contribute key Wnt5 signaling components, allowing Wnt5 to orient the rotation of nascent synapses through a PCP mechanism.
    MeSH term(s) Animals ; Arthropod Antennae/growth & development ; Arthropod Antennae/metabolism ; Axons/metabolism ; Body Patterning ; Dendrites/metabolism ; Drosophila/genetics ; Drosophila/growth & development ; Drosophila/metabolism ; Drosophila Proteins/genetics ; Drosophila Proteins/metabolism ; Gene Expression Regulation, Developmental ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Olfactory Receptor Neurons/metabolism ; Proto-Oncogene Proteins/genetics ; Proto-Oncogene Proteins/metabolism ; Receptor Protein-Tyrosine Kinases/genetics ; Receptor Protein-Tyrosine Kinases/metabolism ; Signal Transduction ; Wnt Proteins/genetics ; Wnt Proteins/metabolism
    Chemical Substances Drosophila Proteins ; Membrane Proteins ; Proto-Oncogene Proteins ; Vang protein, Drosophila ; Wnt Proteins ; Wnt5 protein, Drosophila ; DRL protein, Drosophila (EC 2.7.10.1) ; Receptor Protein-Tyrosine Kinases (EC 2.7.10.1)
    Language English
    Publishing date 2020-05-01
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2186725-2
    ISSN 1553-7404 ; 1553-7390
    ISSN (online) 1553-7404
    ISSN 1553-7390
    DOI 10.1371/journal.pgen.1008767
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: This bud's for you: mechanisms of cellular nucleocytoplasmic trafficking via nuclear envelope budding.

    Fradkin, Lee G / Budnik, Vivian

    Current opinion in cell biology

    2016  Volume 41, Page(s) 125–131

    Abstract: The nuclear envelope (NE) physically separates the cytoplasmic and nuclear compartments. While this barrier provides advantages, it also presents a challenge for the nuclear export of large ribonucleoprotein (RNP) complexes. Decades-old dogma holds that ... ...

    Abstract The nuclear envelope (NE) physically separates the cytoplasmic and nuclear compartments. While this barrier provides advantages, it also presents a challenge for the nuclear export of large ribonucleoprotein (RNP) complexes. Decades-old dogma holds that all such border-crossing is via the nuclear pore complex (NPC). However, the diameter of the NPC central channel limits the passage of large cargos. Here, we review evidence that such large RNPs employ an endogenous NE-budding pathway, previously thought to be exclusive to the nuclear egress of Herpes viruses. We discuss this and other models proposed, the likelihood that this pathway is conserved, and the consequences of disrupting NE-budding for synapse development, localized translation of synaptic mRNAs, and laminopathies inducing accelerated aging.
    MeSH term(s) Active Transport, Cell Nucleus ; Animals ; Herpesviridae/metabolism ; Humans ; Models, Biological ; Nuclear Envelope/metabolism ; Nucleocytoplasmic Transport Proteins/metabolism ; Ribonucleoproteins/metabolism
    Chemical Substances Nucleocytoplasmic Transport Proteins ; Ribonucleoproteins
    Language English
    Publishing date 2016-08
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1026381-0
    ISSN 1879-0410 ; 0955-0674
    ISSN (online) 1879-0410
    ISSN 0955-0674
    DOI 10.1016/j.ceb.2016.05.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Axonal chemokine-like Orion induces astrocyte infiltration and engulfment during mushroom body neuronal remodeling.

    Boulanger, Ana / Thinat, Camille / Züchner, Stephan / Fradkin, Lee G / Lortat-Jacob, Hugues / Dura, Jean-Maurice

    Nature communications

    2021  Volume 12, Issue 1, Page(s) 1849

    Abstract: The remodeling of neurons is a conserved fundamental mechanism underlying nervous system maturation and function. Astrocytes can clear neuronal debris and they have an active role in neuronal remodeling. Developmental axon pruning of Drosophila memory ... ...

    Abstract The remodeling of neurons is a conserved fundamental mechanism underlying nervous system maturation and function. Astrocytes can clear neuronal debris and they have an active role in neuronal remodeling. Developmental axon pruning of Drosophila memory center neurons occurs via a degenerative process mediated by infiltrating astrocytes. However, how astrocytes are recruited to the axons during brain development is unclear. Using an unbiased screen, we identify the gene requirement of orion, encoding for a chemokine-like protein, in the developing mushroom bodies. Functional analysis shows that Orion is necessary for both axonal pruning and removal of axonal debris. Orion performs its functions extracellularly and bears some features common to chemokines, a family of chemoattractant cytokines. We propose that Orion is a neuronal signal that elicits astrocyte infiltration and astrocyte-driven axonal engulfment required during neuronal remodeling in the Drosophila developing brain.
    MeSH term(s) Amino Acid Motifs ; Animals ; Astrocytes/metabolism ; Axons/metabolism ; Chemokines/genetics ; Chemokines/metabolism ; Drosophila/genetics ; Drosophila/growth & development ; Drosophila/metabolism ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Mushroom Bodies/growth & development ; Mushroom Bodies/metabolism ; Mutagenesis ; Neuronal Plasticity/physiology ; Protein Binding ; RNA Interference ; Whole Genome Sequencing
    Chemical Substances Chemokines ; Membrane Proteins
    Language English
    Publishing date 2021-03-23
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-021-22054-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Muscular Dystrophy Model.

    Potikanond, Saranyapin / Nimlamool, Wutigri / Noordermeer, Jasprien / Fradkin, Lee G

    Advances in experimental medicine and biology

    2018  Volume 1076, Page(s) 147–172

    Abstract: Muscular dystrophy (MD) is a group of muscle weakness disease involving in inherited genetic conditions. MD is caused by mutations or alteration in the genes responsible for the structure and functioning of muscles. There are many different types of MD ... ...

    Abstract Muscular dystrophy (MD) is a group of muscle weakness disease involving in inherited genetic conditions. MD is caused by mutations or alteration in the genes responsible for the structure and functioning of muscles. There are many different types of MD which have a wide range from mild symptoms to severe disability. Some types involve the muscles used for breathing which eventually affect life expectancy. This chapter provides an overview of the MD types, its gene mutations, and the Drosophila MD models. Specifically, the Duchenne muscular dystrophy (DMD), the most common form of MD, will be thoroughly discussed including Dystrophin genes, their isoforms, possible mechanisms, and signaling pathways of pathogenesis.
    MeSH term(s) Animals ; Disease Models, Animal ; Drosophila melanogaster ; Humans ; Muscular Dystrophy, Animal
    Language English
    Publishing date 2018-06-27
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2214-8019 ; 0065-2598
    ISSN (online) 2214-8019
    ISSN 0065-2598
    DOI 10.1007/978-981-13-0529-0_9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Htt is a repressor of Abl activity required for APP-induced axonal growth.

    Marquilly, Claire / Busto, Germain U / Leger, Brittany S / Boulanger, Ana / Giniger, Edward / Walker, James A / Fradkin, Lee G / Dura, Jean-Maurice

    PLoS genetics

    2021  Volume 17, Issue 1, Page(s) e1009287

    Abstract: Huntington's disease is a progressive autosomal dominant neurodegenerative disorder caused by the expansion of a polyglutamine tract at the N-terminus of a large cytoplasmic protein. The Drosophila huntingtin (htt) gene is widely expressed during all ... ...

    Abstract Huntington's disease is a progressive autosomal dominant neurodegenerative disorder caused by the expansion of a polyglutamine tract at the N-terminus of a large cytoplasmic protein. The Drosophila huntingtin (htt) gene is widely expressed during all developmental stages from embryos to adults. However, Drosophila htt mutant individuals are viable with no obvious developmental defects. We asked if such defects could be detected in htt mutants in a background that had been genetically sensitized to reveal cryptic developmental functions. Amyloid precursor protein (APP) is linked to Alzheimer's disease. Appl is the Drosophila APP ortholog and Appl signaling modulates axon outgrowth in the mushroom bodies (MBs), the learning and memory center in the fly, in part by recruiting Abl tyrosine kinase. Here, we find that htt mutations suppress axon outgrowth defects of αβ neurons in Appl mutant MB by derepressing the activity of Abl. We show that Abl is required in MB αβ neurons for their axon outgrowth. Importantly, both Abl overexpression and lack of expression produce similar phenotypes in the MBs, indicating the necessity of tightly regulating Abl activity. We find that Htt behaves genetically as a repressor of Abl activity, and consistent with this, in vivo FRET-based measurements reveal a significant increase in Abl kinase activity in the MBs when Htt levels are reduced. Thus, Appl and Htt have essential but opposing roles in MB development, promoting and suppressing Abl kinase activity, respectively, to maintain the appropriate intermediate level necessary for axon growth.
    MeSH term(s) Acyltransferases/genetics ; Alzheimer Disease/genetics ; Alzheimer Disease/pathology ; Amyloid beta-Protein Precursor/genetics ; Animals ; Axonal Transport/genetics ; Axons/metabolism ; Axons/pathology ; Drosophila Proteins/genetics ; Drosophila melanogaster/genetics ; Embryonic Development/genetics ; Humans ; Huntingtin Protein/genetics ; Huntington Disease/genetics ; Huntington Disease/pathology ; Learning/physiology ; Memory/physiology ; Mushroom Bodies/growth & development ; Mushroom Bodies/pathology ; Mutation/genetics ; Nerve Degeneration/genetics ; Nerve Degeneration/pathology ; Neurons/metabolism ; Neurons/pathology ; Signal Transduction/genetics
    Chemical Substances Amyloid beta-Protein Precursor ; Drosophila Proteins ; HTT protein, human ; Htt protein, Drosophila ; Huntingtin Protein ; Acyltransferases (EC 2.3.-) ; App protein, Drosophila (EC 2.3.1.-)
    Language English
    Publishing date 2021-01-19
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2186725-2
    ISSN 1553-7404 ; 1553-7390
    ISSN (online) 1553-7404
    ISSN 1553-7390
    DOI 10.1371/journal.pgen.1009287
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Coordinated changes in the expression of Wnt pathway genes following human and rat peripheral nerve injury.

    van Vliet, Arie C / Lee, Jinhui / van der Poel, Marlijn / Mason, Matthew R J / Noordermeer, Jasprina N / Fradkin, Lee G / Tannemaat, Martijn R / Malessy, Martijn J A / Verhaagen, Joost / De Winter, Fred

    PloS one

    2021  Volume 16, Issue 4, Page(s) e0249748

    Abstract: A human neuroma-in continuity (NIC), formed following a peripheral nerve lesion, impedes functional recovery. The molecular mechanisms that underlie the formation of a NIC are poorly understood. Here we show that the expression of multiple genes of the ... ...

    Abstract A human neuroma-in continuity (NIC), formed following a peripheral nerve lesion, impedes functional recovery. The molecular mechanisms that underlie the formation of a NIC are poorly understood. Here we show that the expression of multiple genes of the Wnt family, including Wnt5a, is changed in NIC tissue from patients that underwent reconstructive surgery. The role of Wnt ligands in NIC pathology and nerve regeneration is of interest because Wnt ligands are implicated in tissue regeneration, fibrosis, axon repulsion and guidance. The observations in NIC prompted us to investigate the expression of Wnt ligands in the injured rat sciatic nerve and in the dorsal root ganglia (DRG). In the injured nerve, four gene clusters were identified with temporal expression profiles corresponding to particular phases of the regeneration process. In the DRG up- and down regulation of certain Wnt receptors suggests that nerve injury has an impact on the responsiveness of injured sensory neurons to Wnt ligands in the nerve. Immunohistochemistry showed that Schwann cells in the NIC and in the injured nerve are the source of Wnt5a, whereas the Wnt5a receptor Ryk is expressed by axons traversing the NIC. Taken together, these observations suggest a central role for Wnt signalling in peripheral nerve regeneration.
    MeSH term(s) Animals ; Disease Models, Animal ; Female ; Ganglia, Spinal/metabolism ; Ganglia, Spinal/pathology ; Gene Expression Regulation ; Humans ; Nerve Regeneration/physiology ; Peripheral Nerve Injuries/genetics ; Peripheral Nerve Injuries/metabolism ; Peripheral Nerve Injuries/pathology ; Rats ; Rats, Wistar ; Sciatic Nerve/metabolism ; Sciatic Nerve/pathology ; Sensory Receptor Cells/metabolism ; Sensory Receptor Cells/pathology ; Wnt Signaling Pathway
    Language English
    Publishing date 2021-04-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0249748
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  7. Article ; Online: Axonal chemokine-like Orion induces astrocyte infiltration and engulfment during mushroom body neuronal remodeling

    Ana Boulanger / Camille Thinat / Stephan Züchner / Lee G. Fradkin / Hugues Lortat-Jacob / Jean-Maurice Dura

    Nature Communications, Vol 12, Iss 1, Pp 1-

    2021  Volume 11

    Abstract: Astrocytes can engulf axonal debris in the developing brain. However, the mechanisms regulating astrocyte recruitment to the proper axons is unclear. Here, the authors identify Orion as a signal for astrocyte infiltration and engulfment to the mushroom ... ...

    Abstract Astrocytes can engulf axonal debris in the developing brain. However, the mechanisms regulating astrocyte recruitment to the proper axons is unclear. Here, the authors identify Orion as a signal for astrocyte infiltration and engulfment to the mushroom bodies in the Drosophila developing brain.
    Keywords Science ; Q
    Language English
    Publishing date 2021-03-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Retrovirus-like Gag Protein Arc1 Binds RNA and Traffics across Synaptic Boutons.

    Ashley, James / Cordy, Benjamin / Lucia, Diandra / Fradkin, Lee G / Budnik, Vivian / Thomson, Travis

    Cell

    2018  Volume 172, Issue 1-2, Page(s) 262–274.e11

    Abstract: Arc/Arg3.1 is required for synaptic plasticity and cognition, and mutations in this gene are linked to autism and schizophrenia. Arc bears a domain resembling retroviral/retrotransposon Gag-like proteins, which multimerize into a capsid that packages ... ...

    Abstract Arc/Arg3.1 is required for synaptic plasticity and cognition, and mutations in this gene are linked to autism and schizophrenia. Arc bears a domain resembling retroviral/retrotransposon Gag-like proteins, which multimerize into a capsid that packages viral RNA. The significance of such a domain in a plasticity molecule is uncertain. Here, we report that the Drosophila Arc1 protein forms capsid-like structures that bind darc1 mRNA in neurons and is loaded into extracellular vesicles that are transferred from motorneurons to muscles. This loading and transfer depends on the darc1-mRNA 3' untranslated region, which contains retrotransposon-like sequences. Disrupting transfer blocks synaptic plasticity, suggesting that transfer of dArc1 complexed with its mRNA is required for this function. Notably, cultured cells also release extracellular vesicles containing the Gag region of the Copia retrotransposon complexed with its own mRNA. Taken together, our results point to a trans-synaptic mRNA transport mechanism involving retrovirus-like capsids and extracellular vesicles.
    MeSH term(s) Animals ; Biological Transport ; Cells, Cultured ; Cytoskeletal Proteins/chemistry ; Cytoskeletal Proteins/genetics ; Cytoskeletal Proteins/metabolism ; Drosophila ; Drosophila Proteins/genetics ; Drosophila Proteins/metabolism ; Gene Products, gag/chemistry ; Gene Products, gag/genetics ; Multivesicular Bodies/metabolism ; Nerve Tissue Proteins/chemistry ; Nerve Tissue Proteins/genetics ; Nerve Tissue Proteins/metabolism ; Neuromuscular Junction/metabolism ; Neuronal Plasticity ; Peptide Hydrolases/genetics ; Peptide Hydrolases/metabolism ; Presynaptic Terminals/metabolism ; Presynaptic Terminals/physiology ; Protein Binding ; Protein Domains ; RNA, Messenger/metabolism ; Retroelements/genetics
    Chemical Substances Cytoskeletal Proteins ; Drosophila Proteins ; Gene Products, gag ; Nerve Tissue Proteins ; RNA, Messenger ; Retroelements ; activity regulated cytoskeletal-associated protein ; Peptide Hydrolases (EC 3.4.-) ; Copia protein, Drosophila (EC 3.4.23.-)
    Language English
    Publishing date 2018-01-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2017.12.022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Large-Scale Production of Wholly Cellular Bioinks via the Optimization of Human Induced Pluripotent Stem Cell Aggregate Culture in Automated Bioreactors.

    Ho, Debbie L L / Lee, Stacey / Du, Jianyi / Weiss, Jonathan D / Tam, Tony / Sinha, Soham / Klinger, Danielle / Devine, Sean / Hamfeldt, Art / Leng, Hope T / Herrmann, Jessica E / He, Mengdi / Fradkin, Lee G / Tan, Tze Kai / Standish, David / Tomasello, Peter / Traul, Donald / Dianat, Noushin / Ladi, Rukmini /
    Vicard, Quentin / Katikireddy, Kishore / Skylar-Scott, Mark A

    Advanced healthcare materials

    2022  Volume 11, Issue 24, Page(s) e2201138

    Abstract: Combining the sustainable culture of billions of human cells and the bioprinting of wholly cellular bioinks offers a pathway toward organ-scale tissue engineering. Traditional 2D culture methods are not inherently scalable due to cost, space, and ... ...

    Abstract Combining the sustainable culture of billions of human cells and the bioprinting of wholly cellular bioinks offers a pathway toward organ-scale tissue engineering. Traditional 2D culture methods are not inherently scalable due to cost, space, and handling constraints. Here, the suspension culture of human induced pluripotent stem cell-derived aggregates (hAs) is optimized using an automated 250 mL stirred tank bioreactor system. Cell yield, aggregate morphology, and pluripotency marker expression are maintained over three serial passages in two distinct cell lines. Furthermore, it is demonstrated that the same optimized parameters can be scaled to an automated 1 L stirred tank bioreactor system. This 4-day culture results in a 16.6- to 20.4-fold expansion of cells, generating approximately 4 billion cells per vessel, while maintaining >94% expression of pluripotency markers. The pluripotent aggregates can be subsequently differentiated into derivatives of the three germ layers, including cardiac aggregates, and vascular, cortical and intestinal organoids. Finally, the aggregates are compacted into a wholly cellular bioink for rheological characterization and 3D bioprinting. The printed hAs are subsequently differentiated into neuronal and vascular tissue. This work demonstrates an optimized suspension culture-to-3D bioprinting pipeline that enables a sustainable approach to billion cell-scale organ engineering.
    MeSH term(s) Humans ; Induced Pluripotent Stem Cells ; Cell Culture Techniques ; Cell Proliferation ; Cell Line ; Bioreactors
    Language English
    Publishing date 2022-11-22
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2649576-4
    ISSN 2192-2659 ; 2192-2640
    ISSN (online) 2192-2659
    ISSN 2192-2640
    DOI 10.1002/adhm.202201138
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  10. Article ; Online: ROR and RYK extracellular region structures suggest that receptor tyrosine kinases have distinct WNT-recognition modes.

    Shi, Fumin / Mendrola, Jeannine M / Sheetz, Joshua B / Wu, Neo / Sommer, Anselm / Speer, Kelsey F / Noordermeer, Jasprina N / Kan, Zhong-Yuan / Perry, Kay / Englander, S Walter / Stayrook, Steven E / Fradkin, Lee G / Lemmon, Mark A

    Cell reports

    2021  Volume 37, Issue 3, Page(s) 109834

    Abstract: WNTs play key roles in development and disease, signaling through Frizzled (FZD) seven-pass transmembrane receptors and numerous co-receptors including ROR and RYK family receptor tyrosine kinases (RTKs). We describe crystal structures and WNT-binding ... ...

    Abstract WNTs play key roles in development and disease, signaling through Frizzled (FZD) seven-pass transmembrane receptors and numerous co-receptors including ROR and RYK family receptor tyrosine kinases (RTKs). We describe crystal structures and WNT-binding characteristics of extracellular regions from the Drosophila ROR and RYK orthologs Nrk (neurospecific receptor tyrosine kinase) and Derailed-2 (Drl-2), which bind WNTs though a FZD-related cysteine-rich domain (CRD) and WNT-inhibitory factor (WIF) domain respectively. Our crystal structures suggest that neither Nrk nor Drl-2 can accommodate the acyl chain typically attached to WNTs. The Nrk CRD contains a deeply buried bound fatty acid, unlikely to be exchangeable. The Drl-2 WIF domain lacks the lipid-binding site seen in WIF-1. We also find that recombinant DWnt-5 can bind Drosophila ROR and RYK orthologs despite lacking an acyl chain. Alongside analyses of WNT/receptor interaction sites, our structures provide further insight into how WNTs may recruit RTK co-receptors into signaling complexes.
    MeSH term(s) Animals ; Drosophila Proteins/genetics ; Drosophila Proteins/metabolism ; Drosophila melanogaster/enzymology ; Drosophila melanogaster/genetics ; Models, Molecular ; Nerve Tissue Proteins/genetics ; Nerve Tissue Proteins/metabolism ; Protein Binding ; Protein Conformation ; Protein Interaction Domains and Motifs ; Protein-Tyrosine Kinases/genetics ; Protein-Tyrosine Kinases/metabolism ; Proto-Oncogene Proteins/genetics ; Proto-Oncogene Proteins/metabolism ; Receptor Protein-Tyrosine Kinases/genetics ; Receptor Protein-Tyrosine Kinases/metabolism ; Sf9 Cells ; Structure-Activity Relationship ; Wnt Proteins/genetics ; Wnt Proteins/metabolism ; Wnt Signaling Pathway
    Chemical Substances Drosophila Proteins ; Nerve Tissue Proteins ; Proto-Oncogene Proteins ; Wnt Proteins ; Wnt5 protein, Drosophila ; dnt protein, Drosophila (EC 2.7.1.-) ; DRL protein, Drosophila (EC 2.7.10.1) ; Nrk protein, Drosophila (EC 2.7.10.1) ; Protein-Tyrosine Kinases (EC 2.7.10.1) ; Receptor Protein-Tyrosine Kinases (EC 2.7.10.1)
    Language English
    Publishing date 2021-10-22
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2021.109834
    Database MEDical Literature Analysis and Retrieval System OnLINE

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