Ero1L, a thiol oxidase, is required for Notch signaling through cysteine bridge formation of the Lin12-Notch repeats in Drosophila melanogaster

Notch-mediated cell–cell communication regulates numerous developmental processes and cell fate decisions. Through a mosaic genetic screen in Drosophila melanogaster, we identified a role in Notch signaling for a conserved thiol oxidase, endoplasmic reticulum (ER) oxidoreductin 1–like (Ero1L). Although Ero1L is reported to play a widespread role in protein folding in yeast, in flies Ero1L mutant clones show specific defects in lateral inhibition and inductive signaling, two characteristic processes regulated by Notch signaling. Ero1L mutant cells accumulate high levels of Notch protein in the ER and induce the unfolded protein response, suggesting that Notch is misfolded and fails to be exported from the ER. Biochemical assays demonstrate that Ero1L is required for formation of disulfide bonds of three Lin12-Notch repeats (LNRs) present in the extracellular domain of Notch. These LNRs are unique to the Notch family of proteins. Therefore, we have uncovered an unexpected requirement for Ero1L in the maturation of the Notch receptor.

[1]  H. Bellen,et al.  Rumi Is a CAP10 Domain Glycosyltransferase that Modifies Notch and Is Required for Notch Signaling , 2008, Cell.

[2]  B. Dickson,et al.  A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila , 2007, Nature.

[3]  J. Dow,et al.  Using FlyAtlas to identify better Drosophila melanogaster models of human disease , 2007, Nature Genetics.

[4]  D. L. Coppock,et al.  Generating Disulfides in Multicellular Organisms: Emerging Roles for a New Flavoprotein Family* , 2007, Journal of Biological Chemistry.

[5]  J. Aster,et al.  Structural basis for autoinhibition of Notch , 2007, Nature Structural &Molecular Biology.

[6]  S. Lovell,et al.  ERp57 is essential for efficient folding of glycoproteins sharing common structural domains , 2007, The EMBO journal.

[7]  H. Steller,et al.  Unfolded protein response in a Drosophila model for retinal degeneration , 2007, The EMBO journal.

[8]  D. Y. Thomas,et al.  ERp57 and PDI: multifunctional protein disulfide isomerases with similar domain architectures but differing substrate-partner associations. , 2006, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[9]  J. Knoblich,et al.  The conserved c2 domain protein lethal (2) giant discs regulates protein trafficking in Drosophila. , 2006, Developmental cell.

[10]  S. Bray Notch signalling: a simple pathway becomes complex , 2006, Nature Reviews Molecular Cell Biology.

[11]  C. Sevier,et al.  Conservation and diversity of the cellular disulfide bond formation pathways. , 2006, Antioxidants & redox signaling.

[12]  H. Bellen,et al.  Senseless physically interacts with proneural proteins and functions as a transcriptional co-activator , 2006, Development.

[13]  H. Bellen,et al.  Senseless and Daughterless confer neuronal identity to epithelial cells in the Drosophila wing margin , 2006, Development.

[14]  Sunil Q. Mehta,et al.  Sec15, a component of the exocyst, promotes notch signaling during the asymmetric division of Drosophila sensory organ precursors. , 2005, Developmental cell.

[15]  A. Xu,et al.  Chaperone Activity of Protein O-Fucosyltransferase 1 Promotes Notch Receptor Folding , 2005, Science.

[16]  R. Kaufman,et al.  ER stress and the unfolded protein response. , 2005, Mutation research.

[17]  L. Ruddock,et al.  The human protein disulphide isomerase family: substrate interactions and functional properties , 2005, EMBO reports.

[18]  A. McMichael,et al.  Structural and functional properties of the human notch-1 ligand binding region. , 2004, Structure.

[19]  G. Struhl,et al.  Drosophila Epsin mediates a select endocytic pathway that DSL ligands must enter to activate Notch , 2004, Development.

[20]  J. Aster,et al.  Notch Subunit Heterodimerization and Prevention of Ligand-Independent Proteolytic Activation Depend, Respectively, on a Novel Domain and the LNR Repeats , 2004, Molecular and Cellular Biology.

[21]  Andrew P. Weng,et al.  Activating Mutations of NOTCH1 in Human T Cell Acute Lymphoblastic Leukemia , 2004, Science.

[22]  L. Giudice,et al.  The Lin12-Notch Repeats of Pregnancy-associated Plasma Protein-A Bind Calcium and Determine Its Proteolytic Specificity* , 2004, Journal of Biological Chemistry.

[23]  Deborah Fass,et al.  Structure of Ero1p, Source of Disulfide Bonds for Oxidative Protein Folding in the Cell , 2004, Cell.

[24]  Eric C. Lai,et al.  Notch signaling: control of cell communication and cell fate , 2004, Development.

[25]  F. Schweisguth,et al.  Regulation of Notch Signaling Activity , 2004, Current Biology.

[26]  F. Schweisguth,et al.  Asymmetric localization and function of cell-fate determinants: a fly’s view , 2004, Current Opinion in Neurobiology.

[27]  K. Irvine,et al.  Glycosylation regulates Notch signalling , 2003, Nature Reviews Molecular Cell Biology.

[28]  P. Hiesinger,et al.  Mapping Drosophila mutations with molecularly defined P element insertions , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[29]  J. Aster,et al.  Nuclear magnetic resonance structure of a prototype Lin12-Notch repeat module from human Notch1. , 2003, Biochemistry.

[30]  R. Mann,et al.  Boca, an Endoplasmic Reticulum Protein Required for Wingless Signaling and Trafficking of LDL Receptor Family Members in Drosophila , 2003, Cell.

[31]  T. Kudo,et al.  Presenilins mediate a dual intramembranous γ‐secretase cleavage of Notch‐1 , 2002 .

[32]  M. Gonzalez-Gaitan,et al.  The endocytic protein alpha-Adaptin is required for numb-mediated asymmetric cell division in Drosophila. , 2002, Developmental cell.

[33]  S. Kidd,et al.  Furin cleavage is not a requirement for Drosophila Notch function , 2002, Mechanisms of Development.

[34]  M. W. Young,et al.  kuzbanian-mediated cleavage of Drosophila Notch. , 2002, Genes & development.

[35]  H. Johnston,et al.  Delta signaling from the germ line controls the proliferation and differentiation of the somatic follicle cells during Drosophila oogenesis , 2001 .

[36]  Liqun Luo,et al.  Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development , 2001, Trends in Neurosciences.

[37]  J. Weissman,et al.  Biochemical basis of oxidative protein folding in the endoplasmic reticulum. , 2000, Science.

[38]  I. Braakman,et al.  The CXXCXXC motif determines the folding, structure and stability of human Ero1‐Lα , 2000, The EMBO journal.

[39]  H. Bellen,et al.  Senseless, a Zn Finger Transcription Factor, Is Necessary and Sufficient for Sensory Organ Development in Drosophila , 2000, Cell.

[40]  N. Bulleid,et al.  Endoplasmic Reticulum Oxidoreductin 1-Lβ (ERO1-Lβ), a Human Gene Induced in the Course of the Unfolded Protein Response* 210 , 2000, The Journal of Biological Chemistry.

[41]  J. C. Clemens,et al.  Use of double-stranded RNA interference in Drosophila cell lines to dissect signal transduction pathways. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[42]  Peter Walter,et al.  Functional and Genomic Analyses Reveal an Essential Coordination between the Unfolded Protein Response and ER-Associated Degradation , 2000, Cell.

[43]  G M Rubin,et al.  A Drosophila complementary DNA resource. , 2000, Science.

[44]  M. Rocchi,et al.  ERO1-L, a Human Protein That Favors Disulfide Bond Formation in the Endoplasmic Reticulum* , 2000, The Journal of Biological Chemistry.

[45]  B. Dickson,et al.  Analysis of Drosophila photoreceptor axon guidance in eye-specific mosaics. , 2000, Development.

[46]  Q. T. Wang,et al.  The subcellular localization and activity of Drosophila cubitus interruptus are regulated at multiple levels. , 1999, Development.

[47]  J. Burnside,et al.  Homology between Egg White Sulfhydryl Oxidase and Quiescin Q6 Defines a New Class of Flavin-linked Sulfhydryl Oxidases* , 1999, The Journal of Biological Chemistry.

[48]  C. Kaiser,et al.  Ero1p oxidizes protein disulfide isomerase in a pathway for disulfide bond formation in the endoplasmic reticulum. , 1999, Molecular cell.

[49]  M. Gho,et al.  Revisiting the Drosophila microchaete lineage: a novel intrinsically asymmetric cell division generates a glial cell. , 1999, Development.

[50]  H. Gilbert,et al.  Sulfhydryl Oxidase from Egg White , 1999, The Journal of Biological Chemistry.

[51]  T. Schwarz,et al.  A genetic method for generating Drosophila eyes composed exclusively of mitotic clones of a single genotype. , 1999, Genetics.

[52]  F. Elefant,et al.  Tissue-specific expression of dominant negative mutant Drosophila HSC70 causes developmental defects and lethality. , 1999, Molecular biology of the cell.

[53]  S. Artavanis-Tsakonas,et al.  Notch Signaling : Cell Fate Control and Signal Integration in Development , 1999 .

[54]  Iva Greenwald,et al.  Presenilin is required for activity and nuclear access of Notch in Drosophila , 1999, Nature.

[55]  William J. Ray,et al.  A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain , 1999, Nature.

[56]  S. Bray,et al.  Notch signalling in Drosophila: three ways to use a pathway. , 1998, Seminars in cell & developmental biology.

[57]  H. Inokuchi,et al.  Respiratory chain is required to maintain oxidized states of the DsbA-DsbB disulfide bond formation system in aerobically growing Escherichia coli cells. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[58]  S. Bray,et al.  Feed-back mechanisms affecting Notch activation at the dorsoventral boundary in the Drosophila wing. , 1997, Development.

[59]  T. Schedl,et al.  Germ-line tumor formation caused by activation of glp-1, a Caenorhabditis elegans member of the Notch family of receptors. , 1997, Development.

[60]  C. Heldin,et al.  Identification of Smad2, a Human Mad-related Protein in the Transforming Growth Factor β Signaling Pathway* , 1997, The Journal of Biological Chemistry.

[61]  G. Morata,et al.  Visualization of Gene Expression in Living Adult Drosophila , 1996, Science.

[62]  Richard D Fetter,et al.  Genetic Dissection of Structural and Functional Components of Synaptic Plasticity. I. Fasciclin II Controls Synaptic Stabilization and Growth , 1996, Neuron.

[63]  W. Brook,et al.  Antagonistic Interactions Between Wingless and Decapentaplegic Responsible for Dorsal-Ventral Pattern in the Drosophila Leg , 1996, Science.

[64]  I. Campbell,et al.  Solution Structure of a Pair of Calcium-Binding Epidermal Growth Factor-like Domains: Implications for the Marfan Syndrome and Other Genetic Disorders , 1996, Cell.

[65]  C. K. Motzny,et al.  The Drosophila cubitus interruptus protein and its role in the wingless and hedgehog signal transduction pathways , 1995, Mechanisms of Development.

[66]  G. Rubin,et al.  A genetic analysis of the 63E-64A genomic region of Drosophila melanogaster: identification of mutations in a replication factor C subunit. , 1995, Genetics.

[67]  S. Artavanis-Tsakonas,et al.  Cytosolic interaction between deltex and Notch ankyrin repeats implicates deltex in the Notch signaling pathway. , 1994, Development.

[68]  H. Jäckle,et al.  spalt encodes an evolutionarily conserved zinc finger protein of novel structure which provides homeotic gene function in the head and tail region of the Drosophila embryo. , 1994, The EMBO journal.

[69]  Y. Jan,et al.  HLH proteins, fly neurogenesis, and vertebrate myogenesis , 1993, Cell.

[70]  M. W. Young,et al.  Antineurogenic phenotypes induced by truncated Notch proteins indicate a role in signal transduction and may point to a novel function for Notch in nuclei. , 1993, Genes & development.

[71]  U. Tepass,et al.  Crumbs and stardust act in a genetic pathway that controls the organization of epithelia in Drosophila melanogaster. , 1993, Developmental biology.

[72]  N. Perrimon,et al.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. , 1993, Development.

[73]  Y. Jan,et al.  Cell interactions and gene interactions in peripheral neurogenesis. , 1993, Genes & development.

[74]  S. Artavanis-Tsakonas,et al.  The involvement of the Notch locus in Drosophila oogenesis. , 1992, Development.

[75]  S. Carroll,et al.  Control of Drosophila wing and haltere development by the nuclear vestigial gene product. , 1991, Genes & development.

[76]  K. White,et al.  Characterization and spatial distribution of the ELAV protein during Drosophila melanogaster development. , 1991, Journal of neurobiology.

[77]  V. Hartenstein,et al.  A dual function of the Notch gene in Drosophila sensillum development. , 1990, Developmental biology.

[78]  Y. Jan,et al.  Patterns of expression of cut, a protein required for external sensory organ development in wild-type and cut mutant Drosophila embryos. , 1990, Genes & development.

[79]  G. Seydoux,et al.  Analysis of gain-of-function mutations of the lin-12 gene of Caenorhabditis elegans , 1990, Nature.

[80]  Tian Xu,et al.  Molecular interactions between the protein products of the neurogenic loci Notch and Delta, two EGF-homologous genes in Drosophila , 1990, Cell.

[81]  R. Freedman Protein disulfide isomerase: Multiple roles in the modification of nascent secretory proteins , 1989, Cell.

[82]  T. Kudo,et al.  Presenilins mediate a dual intramembranous gamma-secretase cleavage of Notch-1. , 2002, The EMBO journal.

[83]  D. St Johnston,et al.  Delta signaling from the germ line controls the proliferation and differentiation of the somatic follicle cells during Drosophila oogenesis. , 2001, Genes & development.

[84]  N. Bulleid,et al.  Endoplasmic reticulum oxidoreductin 1-lbeta (ERO1-Lbeta), a human gene induced in the course of the unfolded protein response. , 2000, The Journal of biological chemistry.

[85]  T. Tabata,et al.  Hedgehog creates a gradient of DPP activity in Drosophila wing imaginal discs. , 2000, Molecular cell.

[86]  N E Baker,et al.  Several levels of EGF receptor signaling during photoreceptor specification in wild-type, Ellipse, and null mutant Drosophila. , 1999, Developmental biology.

[87]  J. Weissman,et al.  Ero1p: a novel and ubiquitous protein with an essential role in oxidative protein folding in the endoplasmic reticulum. , 1998, Molecular cell.

[88]  C. Kaiser,et al.  The ERO1 gene of yeast is required for oxidation of protein dithiols in the endoplasmic reticulum. , 1998, Molecular cell.

[89]  J. Modolell Patterning of the adult peripheral nervous system of Drosophila. , 1997, Perspectives on developmental neurobiology.

[90]  A. Garcı́a-Bellido,et al.  Activation and function of Notch at the dorsal-ventral boundary of the wing imaginal disc. , 1996, Development.

[91]  A. Garcı́a-Bellido,et al.  Modifications of the notch function by Abruptex mutations in Drosophila melanogaster. , 1994, Genetics.

[92]  J. Aster,et al.  Nuclear Magnetic Resonance Structure of a Prototype Lin 12-Notch Repeat Module from Human Notch 1 † , 2022 .