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JOURNAL ARTICLES
Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development
F.F. Del Amo, D.E. Smith, P.J. Swiatek, M. Gendron-Maguire, R.J. Greenspan, A.P. McMahon, T. Gridley
Development 1992 115: 737-744;
F.F. Del Amo
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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D.E. Smith
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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P.J. Swiatek
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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M. Gendron-Maguire
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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R.J. Greenspan
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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A.P. McMahon
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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T. Gridley
Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.
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Summary

The Notch gene of Drosophila encodes a large transmembrane protein involved in cell-cell interactions and cell fate decisions in the Drosophila embryo. To determine if a gene homologous to Drosophila Notch plays a role in early mouse development, we screened a mouse embryo cDNA library with probes from the Xenopus Notch homolog, Xotch. A partial cDNA clone encoding the mouse Notch homolog, which we have termed Motch, was used to analyze expression of the Motch gene. Motch transcripts were detected in a wide variety of adult tissues, which included derivatives of all three germ layers. Differentiation of P19 embryonal carcinoma cells into neuronal cell types resulted in increased expression of Motch RNA. In the postimplantation mouse embryo Motch transcripts were first detected in mesoderm at 7.5 days post coitum (dpc). By 8.5 dpc, transcript levels were highest in presomitic mesoderm, mesenchyme and endothelial cells, while much lower levels were detected in neuroepithelium. In contrast, at 9.5 dpc, neuroepithelium was a major site of Motch expression. Transcripts were also abundant in cell types derived from neural crest. These data suggest that the Motch gene plays multiple roles in patterning and differentiation of the early postimplantation mouse embryo.

REFERENCES

    1. Apella E.,
    2. Robinson E. A.,
    3. Ullrich S. J.,
    4. Stoppelli M. P.,
    5. Corti A.,
    6. Cassani G.,
    7. Blasi F.
    (1987) The receptor-binding sequence of urokinase. J. Biol. Chem 262, 4437–4440
    OpenUrlAbstract/FREE Full Text
    1. Artavanis-Tsakonas S.,
    2. Delidakis C.,
    3. Fehon R. G.
    (1991) The Notch locus and the cell biology of neuroblast segregation. Ann. Rev. Cell Biol 7, 427–452
    OpenUrlCrossRefWeb of Science
    1. Artavanis-Tsakonas S.,
    2. Simpson P.
    (1991) Choosing a cell fate: a view from the Notch locus. Trends Genet 7, 403–408
    OpenUrlCrossRefPubMedWeb of Science
    1. Austin J.,
    2. Kimble J.
    (1987) glp-1 is required in the germ line for regulation of the decision between mitosis and meiosis in C. elegans. Cell 51, 589–599
    OpenUrlCrossRefPubMedWeb of Science
    1. Aves S. J.,
    2. Durkacz B. W.,
    3. Carr A.,
    4. Nurse P.
    (1985) Cloning, sequencing, and transcriptional control of the Schizosaccharomyces pombe cdc10 start gene. EMBO J 4, 457–463
    OpenUrlPubMedWeb of Science
    1. Beddington R. S. P.
    (1981) An autoradiographic analysis of the potency of embryonic ectoderm in the 8th day postimplantation mouse embryo. J. Embryol. exp. Morph 64, 87–104
    OpenUrlPubMedWeb of Science
    1. Beddington R. S. P.
    (1982) An autoradiographic analysis of tissue potency in different regions of the embryonic ectoderm during gastrulation in the mouse. J. Embryol. exp. Morph 69, 265–285
    OpenUrlPubMedWeb of Science
    1. Bevilacqua M. P.,
    2. Stengelin S.,
    3. Gimbrone M. A.,
    4. Seed B.
    (1989) Endothelial leukocyte adhesion molecule 1: an inducible receptor for neutrophils related to complement regulatory proteins and lectins. Science 243, 1160–1165
    OpenUrlAbstract/FREE Full Text
    1. Breeden L.,
    2. Nasmyth K.
    (1987) Similarity between cell-cycle genes of budding yeast and fission yeast and the Notch gene of Drosophila. Nature 329, 651–654
    OpenUrlCrossRefPubMed
    1. Cagan R. L.,
    2. Ready D. F.
    (1989) Notch is required for successivecell decisions in the developing Drosophila retina. Genes Dev 3, 1099–1112
    OpenUrlAbstract/FREE Full Text
    1. Campos-Ortega J. A.,
    2. Knust E.
    (1990) Genetics of early neurogenesis in Drosophila melanogaster. Ann. Rev. Genet 24, 387–407
    OpenUrlCrossRefPubMedWeb of Science
    1. Chisaka O.,
    2. Capecchi M. R.
    (1991). Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5. Nature 350, 473–479
    OpenUrlCrossRefPubMed
    1. Chomczynski P.,
    2. Sacchi N.
    (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem 162, 156–159
    OpenUrlCrossRefPubMedWeb of Science
    1. Coffman C.,
    2. Harris W.,
    3. Kintner C.
    (1990) Xotch, the Xenopus homolog of Drosophila Notch. Science 249, 1438–1441
    OpenUrlAbstract/FREE Full Text
    1. Corbin V.,
    2. Michelson A. M.,
    3. Abmayr S. M.,
    4. Neel V.,
    5. Alcamo E.,
    6. Maniatis T.,
    7. Young M. W.
    (1991) A role for the Drosophila neurogenic genes in mesoderm differentiation. Cell 67, 311–323
    OpenUrlCrossRefPubMedWeb of Science
    1. Davis C. G.
    (1990) The many faces of epidermal growth factor repeats. New Biologist 2, 410–419
    OpenUrlPubMed
    1. Davis L. H.,
    2. Bennett V.
    (1990) Mapping the binding sites of human erythrocyte ankyrin for the anion exchanger and spectrin. J. Biol. Chem 265, 10589–10596
    OpenUrlAbstract/FREE Full Text
    1. de Celis J. F.,
    2. Mari-Beffa M.,
    3. Garcia-Bellido A.
    (1991) Cell-autonomous role of Notch, an epidermal growth factor homologue, in sensory organ differentiation in Drosophila. Proc. Natl. Acad. Sci. USA 88, 632–636
    OpenUrlAbstract/FREE Full Text
    1. Doe C. Q.,
    2. Goodman C. S.
    (1985) Early events in insect neurogenesis. II. The role of cell interactions and cell lineage in the determination of neuronal precursor cells. Dev. Biol 111, 206–219
    OpenUrlCrossRefPubMedWeb of Science
    1. Ellisen L. W.,
    2. Bird J.,
    3. West D. C.,
    4. Soreng A. L.,
    5. Reynolds T. C.,
    6. Smith S. D.,
    7. Sklar J.
    (1991) TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms. Cell 66, 649–661
    OpenUrlCrossRefPubMedWeb of Science
    1. Fahrner K.,
    2. Hogan B. L. M.,
    3. Flavell R. A.
    (1987) Transcription of the H-2 and Qa genes in embryonic and adult mice. EMBO J 6, 1265–1271
    OpenUrlPubMed
    1. Fehon R. G.,
    2. Johansen K.,
    3. Rebay I.,
    4. Artavanis-Tsakonas S.
    (1991) Complex cellular and subcellular regulation of Notch expression during embryonic and imaginal development of Drosophila: implications for Notch function. J. Cell Biol 113, 657–669
    OpenUrlAbstract/FREE Full Text
    1. Fehon R. G.,
    2. Kooh P. J.,
    3. Rebay I.,
    4. Regan C. L.,
    5. Xu T.,
    6. Muskavitch M. A. T.,
    7. Artavanis-Tsakonas S.
    (1990) Molecular interactions between the protein products of the neurogenic loci Notch and Delta, two EGF-homologous genes in Drosophila. Cell 61, 523–534
    OpenUrlCrossRefPubMedWeb of Science
    1. Gallahan D.,
    2. Kozak C.,
    3. Callahan R.
    (1987) A new common integration region (int-3) for mouse mammary tumor virus on mouse chromosome 17. J. Virol 61, 218–220
    OpenUrlAbstract/FREE Full Text
    1. Greenspan R. J.
    (1990) The Notch gene, adhesion, and developmental fate in the Drosophila embryo. New Biologist 2, 595–600
    OpenUrlPubMed
    1. Greenwald I.,
    2. Rubin G. M.
    (1992) Making a difference: the role of cell-cell interactions in establishing separate identities for equivalent cells. Cell 68, 271–281
    OpenUrlCrossRefPubMedWeb of Science
    1. Gridley T.
    (1991) Insertional versus targeted mutagenesis in mice. New Biologist 3, 1025–1034
    OpenUrlPubMedWeb of Science
    1. Gridley T.,
    2. Gray D. A.,
    3. Orr-Weaver T.,
    4. Soriano P.,
    5. Barton D. E.,
    6. Francke U.,
    7. Jaenisch R.
    (1990) Molecular analysis of the Mov-34 mutation: transcript disrupted by proviral integration in mice is conserved in Drosophila. Development 109, 235–242
    OpenUrlAbstract
    1. Gridley T.,
    2. Jaenisch R.,
    3. Gendron-Maguire M.
    (1991) The murine Mov-34 gene: full-length cDNA and genomic organization. Genomics 11, 501–507
    OpenUrlCrossRefPubMedWeb of Science
    1. Hartenstein V.,
    2. Posakony J. W.
    (1990) A dual function of the Notch gene in Drosophila sensillum development. Dev. Biol 142, 13–30
    OpenUrlCrossRefPubMedWeb of Science
    1. Heitzler P.,
    2. Simpson P.
    (1991) The choice of cell fate in the epidermis of Drosophila. Cell 64, 1083–1092
    OpenUrlCrossRefPubMedWeb of Science
    1. Hoppe P. E.,
    2. Greenspan R. J.
    (1990) The Notch locus of Drosophila is required in epidermal cells for epidermal development. Development 109, 875–885
    OpenUrlAbstract/FREE Full Text
    1. Jhappan C.,
    2. Gallahan D.,
    3. Stahle C.,
    4. Chu E.,
    5. Smith G. H.,
    6. Merlino G.,
    7. Callahan R.
    (1992) Expression of an activated Notch -related Int-3 transgene interferes with cell differentiation and induces neoplastic transformation in mammary and salivary glands. Genes Dev 6, 345–355
    OpenUrlAbstract/FREE Full Text
    1. Jones F. S.,
    2. Burgoon M. P.,
    3. Hoffman S.,
    4. Crossin K. L.,
    5. Cunningham B. A.,
    6. Edelman G. M.
    (1988) A cDNA clone for cytotactin contains sequences similar to epidermal growth factor-like repeats and segments of fibronectin and fibrinogen. Proc. Natl. Acad. Sci. USA 85, 2186–2190
    OpenUrlAbstract/FREE Full Text
    1. Joyner A. L.,
    2. Herrup K.,
    3. Auerbach B. A.,
    4. Davis C. A.,
    5. Rossant J.
    (1991) Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox. Science 251, 1239–1243
    OpenUrlAbstract/FREE Full Text
    1. Kessel M.,
    2. Gruss P.
    (1990) Murine developmental control genes. Science 249, 374–379
    OpenUrlAbstract/FREE Full Text
    1. Kidd S.,
    2. Baylies M. K.,
    3. Gasic G. P.,
    4. Young M. W.
    (1989) Structure and distribution of the Notch protein in developing Drosophila. Genes Dev 3, 1113–1129
    OpenUrlAbstract/FREE Full Text
    1. Kidd S.,
    2. Kelley M. R.,
    3. Young M. W.
    (1986) Sequence of the Notch locus of Drosophila melanogaster: relationship of the encoded protein to mammalian clotting and growth factors. Mol. Cell. Biol 6, 3094–3108
    OpenUrlAbstract/FREE Full Text
    1. Kinloch R. A.,
    2. Roller R. J.,
    3. Fimiani C. M.,
    4. Wassarman P. A.
    (1988) Primary structure of the mouse sperm receptor polypeptide determined by genomic cloning. Proc. Natl. Acad. Sci. USA 85, 6409–6413
    OpenUrlAbstract/FREE Full Text
    1. Kurosawa S.,
    2. Stearns D. J.,
    3. Jackson K. W.,
    4. Esmon C. T.
    (1988) A 19-kDa cyanogen bromide freagment from the epidermal growth factor homology domain of rabbit thrombomodulin contains the primary thrombin binding site. J. Biol. Chem 263, 5993–5996
    OpenUrlAbstract/FREE Full Text
    1. Lawler J.,
    2. Hynes R. O.
    (1986) The structure of human thrombospondin, an adhesive glycoprotein with multiple calcium-binding sites and homologies with several different proteins. J. Cell Biol 103, 1635–1648
    OpenUrlAbstract/FREE Full Text
    1. Lux S. E.,
    2. John K. M.,
    3. Bennett V.
    (1990) Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins. Nature 344, 36–42
    OpenUrlCrossRefPubMed
    1. Maine E. M.,
    2. Kimble J.
    (1990) Genetic control of cell communication in C. elegans development. BioEssays 12, 265–271
    OpenUrlCrossRefPubMedWeb of Science
    1. Mann K.,
    2. Deutzmann R.,
    3. Aumailley M.,
    4. Timpl R.,
    5. Raimondi L.,
    6. Yamada Y.,
    7. Pan T.,
    8. Conway D.,
    9. Chu M.
    (1989) Amino acid sequence of mouse nidogen, a multidomain basement membrane protein with binding activity for laminin, collagen IV and cells. EMBO J 8, 65–72
    OpenUrlPubMedWeb of Science
    1. Markopoulou K.,
    2. Artavanis-Tsakonas S.
    (1989) The expression of the neurogenic locus Notch during the postembryonic development of Drosophila melanogaster and its relationship to mitotic activity. J. Neurogenetics 6, 11–26
    OpenUrlCrossRefPubMed
    1. Markopoulou K.,
    2. Artavanis-Tsakonas S.
    (1991) Developmental analysis of the facets, a group of intronic mutations at the Notch locus of Drosophila melanogaster that affect postembryonic development. J. Exp. Zool 257, 314–329
    OpenUrlCrossRefPubMed
    1. McMahon A. P.,
    2. Bradley A.
    (1990) The wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain. Cell 62, 1073–1085
    OpenUrlCrossRefPubMedWeb of Science
    1. Montell D. J.,
    2. Goodman C. S.
    (1988) Drosophila substrate adhesion molecule: sequence of laminin B1 chain reveals domains of homology with mouse. Cell 56, 463–473
    OpenUrl
    1. Ohno H.,
    2. Takimoto G.,
    3. McKeithan T. W.
    (1990) The candidate proto-oncogene bcl-3 is related to genes implicated in cell lineage determination and cell cycle control. Cell 60, 991–997
    OpenUrlCrossRefPubMedWeb of Science
    1. Portin P.
    (1975) Allelic negative complementation of the Abruptex locus of Drosophila melanogaster. Genetics 81, 121–123
    OpenUrlAbstract/FREE Full Text
    1. Poulson D. F.
    (1937) Chromosomal deficiencies and embryonic development of Drosophila melanogaster. Proc. Natl. Acad. Sci. USA 23, 133–137
    OpenUrlFREE Full Text
    1. Rebay I.,
    2. Fleming R. J.,
    3. Fehon R. G.,
    4. Cherbas L.,
    5. Cherbas P.,
    6. Artavanis-Tsakonas S.
    (1991) Specific EGF repeats of Notch mediate interactions with Delta and Serrate: implications for Notch as a multifunctional receptor. Cell 67, 687–699
    OpenUrlCrossRefPubMedWeb of Science
    1. Robbins J.,
    2. Blondel B. J.,
    3. Gallahan D.,
    4. Callahan R.
    (1992) Mouse mammary tumor gene Int-3: a member of the Notch gene family transforms mammary epithelial cells. J. Virol 66, 2594–2599
    OpenUrlAbstract/FREE Full Text
    1. Ruohola H.,
    2. Bremer K. A.,
    3. Baker D.,
    4. Swedlow J. R.,
    5. Jan L. Y.,
    6. Jan Y. N.
    (1991) Role of neurogenic genes in establishment of follicle cell fate and oocyte polarity during oogenesis in Drosophila. Cell 66, 433–449
    OpenUrlCrossRefPubMedWeb of Science
    1. Seydoux G.,
    2. Greenwald I.
    (1989) Cell autonomy of lin-12 function in a cell fate decision in C. elegans. Cell 57, 1237–1245
    OpenUrlCrossRefPubMedWeb of Science
    1. Siegelman M. H.,
    2. van de Rijn M.,
    3. Weissman I. L.
    (1989) Mouse lymph node homing receptor cDNA clone encodes a glycoprotein revealing tandem interaction domains. Science 243, 1165–1172
    OpenUrlAbstract/FREE Full Text
    1. Simpson P.
    (1990) Notch and the choice of cell fate in Drosophila neuroepithelium. Trends Genet 6, 343–345
    OpenUrlCrossRefPubMed
    1. Spence A. M.,
    2. Coulson A.,
    3. Hodkin J.
    (1990) The product of fem-1, a nematode sex-determining gene, contains a motif found in cell cycle control proteins and receptors for cell-cell interactions. Cell 60, 981–990
    OpenUrlCrossRefPubMedWeb of Science
    1. Sudhof T. C.,
    2. Goldstein J. L.,
    3. Brown M. S.,
    4. Russell D. W.
    (1985) The LDL receptor gene: a mosaic of exons shared with different proteins. Science 228, 815–822
    OpenUrlAbstract/FREE Full Text
    1. Suzuki K.,
    2. Kusumoto H.,
    3. Deyashiki Y.,
    4. Nishioka J.,
    5. Maruyama I.,
    6. Zushi M.,
    7. Kawahara S.,
    8. Honda G. T.,
    9. Yamamoto S.,
    10. Horiguchi S.
    (1987) Structure and expression of human thrombomodulin receptor on endothelium acting as a cofactor for protein C activation. EMBO J 6, 1891–1897
    OpenUrlPubMedWeb of Science
    1. Tam P. P. L.,
    2. Beddington R. S. P.
    (1987) The formation of mesodermal tissues in the mouse embryo during gastrulation and early organogenesis. Development 99, 109–126
    OpenUrlAbstract
    1. Technau G. M.,
    2. Campos-Ortega J. A.
    (1987) Cell autonomy of expression of neurogenic genes of Drosophila melanogaster. Proc. Natl. Acad. Sci. USA 84, 4500–4504
    OpenUrlAbstract/FREE Full Text
    1. Thompson C. C.,
    2. Brown T. A.,
    3. McKnight S. L.
    (1991) Convergence of Ets- and Notch -related structural motifs in a heteromeric DNA binding complex. Science 253, 762–768
    OpenUrlAbstract/FREE Full Text
    1. Weinmaster G.,
    2. Roberts V. J.,
    3. Lemke G.
    (1991) A homolog of Drosophila Notch expressed during mammalian development. Development 113, 199–205
    OpenUrlAbstract
    1. Wharton K. A.,
    2. Johansen K. M.,
    3. Xu T.,
    4. Artavanis-Tsakonas S.
    (1985) Nucleotide sequence from the neurogenic locus Notch implies a gene product that shares homology with proteins containing EGF-like repeats. Cell 43, 567–581
    OpenUrlCrossRefPubMedWeb of Science
    1. Xu T.,
    2. Rebay I.,
    3. Fleming R. J.,
    4. Scottgale T. N.,
    5. Artavanis-Tsakonas S.
    (1990) The Notch locus and the genetic circuitry involved in early Drosophila neurogenesis. Genes Dev 4, 464–475
    OpenUrlAbstract/FREE Full Text
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JOURNAL ARTICLES
Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development
F.F. Del Amo, D.E. Smith, P.J. Swiatek, M. Gendron-Maguire, R.J. Greenspan, A.P. McMahon, T. Gridley
Development 1992 115: 737-744;
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JOURNAL ARTICLES
Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development
F.F. Del Amo, D.E. Smith, P.J. Swiatek, M. Gendron-Maguire, R.J. Greenspan, A.P. McMahon, T. Gridley
Development 1992 115: 737-744;

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