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JOURNAL ARTICLES
The fat facets gene is required for Drosophila eye and embryo development
J.A. Fischer-Vize, G.M. Rubin, R. Lehmann
Development 1992 116: 985-1000;
J.A. Fischer-Vize
Howard Hughes Medical Institute, Department of Molecular and Cellular Biology, University of California, Berkeley 94720.
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G.M. Rubin
Howard Hughes Medical Institute, Department of Molecular and Cellular Biology, University of California, Berkeley 94720.
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R. Lehmann
Howard Hughes Medical Institute, Department of Molecular and Cellular Biology, University of California, Berkeley 94720.
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Summary

In a screen for mutations affecting Drosophila eye development, we have identified a gene called fat facets (faf) which is required for cell interactions that prevent particular cells in the developing eye from becoming photoreceptors. Analysis of eyes mosaic for faf+ and faf- cells shows that faf is required in cells near to, but outside, normal developing photoreceptors and also outside of the ectopic photoreceptors in mutant facets. faf is also essential during oogenesis, and we show that a faf-lacZ hybrid protein is localized via the first 392 amino acids of faf to the posterior pole of oocytes. Posterior localization of faf-lacZ depends on oskar. oskar encodes a key organizer of the pole plasm, a specialized cytoplasm at the posterior pole of embryos. The pole plasm is required for germ cell formation and contains the determinant of posterior polarity, encoded by nanos. Although other pole plasm components are required for localization of nanos RNA or for nanos protein function, faf is not. We have cloned the faf gene, and have shown that it encodes two similar large (approximately 300 × 10(3) M(r)) proteins that are unique with respect to other known proteins.

REFERENCES

    1. Baker N. E.,
    2. Mlodzik M.,
    3. Rubin G. M.
    (1990) Spacing differentiation in the developing Drosophila eye: A fibrinogen-related lateral inhibitor encoded by scabrous. Science 250, 1370–1377
    OpenUrlAbstract/FREE Full Text
    1. Banerjee U.,
    2. Zipursky S. L.
    (1990) The role of cell-cell interactions in the development of the Drosophila visual system. Neuron 4, 177–187
    OpenUrlCrossRefPubMedWeb of Science
    1. Boswell R. E.,
    2. Prout M. E.,
    3. Steichen J. C.
    (1991) Mutations in a newly identified Drosophila melanogaster gene, mago nashi, disrupt germ cell formation of mirror-image symmetrical double abdomen embryos. Development 113, 373–384
    OpenUrlAbstract
    1. Carthew R. W.,
    2. Rubin G. M.
    (1990) seven in absentia, a gene required for specification of R7 cell fate in the Drosophila eye. Cell 63, 561–577
    OpenUrlCrossRefPubMedWeb of Science
    1. Cavener D.
    (1987) Comparison of the consensus sequences flanking translational start-sites in Drosophila and vertebrates. Nucl. Acids Res 15, 1353–1361
    OpenUrlAbstract/FREE Full Text
    1. Ephrussi A. E.,
    2. Dickinson L. K.,
    3. Lehmann R.
    (1991) oskar organizes the germ plasm and directs localization of the posterior determinant nanos. Cell 66, 37–50
    OpenUrlCrossRefPubMedWeb of Science
    1. Fischer-Vize J. A.,
    2. Vize P. D.,
    3. Rubin G. M.
    (1992) A unique mutation in the Enhancer of split gene complex affects the fates of the mystery cells in the developing Drosophila eye. Development 115, 89–101
    OpenUrlAbstract
    1. Foe V. E.,
    2. Alberts B. M.
    (1983) Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis. J. Cell. Sci 61, 31–70
    OpenUrlAbstract/FREE Full Text
    1. Freeman M.,
    2. Klämbt C.,
    3. Goodman C. S.,
    4. Rubin G. M.
    (1992) The argos gene encodes a diffusible factor that regulates cell fate decisions in the Drosophila eye. Cell 69, 963–975
    OpenUrlCrossRefPubMedWeb of Science
    1. Fujita S. C.,
    2. Zipursky S. L.,
    3. Benzer S.,
    4. Ferrus A.,
    5. Shotwell S. L.
    (1982) Monoclonal antibodies against the Drosophila nervous system. Proc. Natn. Acad. Sci. USA 79, 7929–7933
    OpenUrlAbstract/FREE Full Text
    1. Hay B.,
    2. Jan L. Y.,
    3. Jan Y. N.
    (1988) A protein component of Drosophila polar granules is encoded by vasa and has extensive sequence similarity to ATP-dependent helicases. Cell 55, 577–587
    OpenUrlCrossRefPubMedWeb of Science
    1. Hay B.,
    2. Ackerman L.,
    3. Barbel S.,
    4. Jan L. Y.,
    5. Jan Y. N.
    (1988) Identification of a component of Drosophila polar granules. Development 103, 625–640
    OpenUrlAbstract/FREE Full Text
    1. Hay B.,
    2. Jan L. Y.,
    3. Jan Y. N.
    (1990) Localization of vasa, a component of Drosophila polar granules, in maternal-effect mutants that alter embryonic anteroposterior polarity. Development 109, 425–433
    OpenUrlAbstract
    1. Hafen E.,
    2. Basler K.,
    3. Edstroem J. E.,
    4. Rubin G. M.
    (1987) sevenless, a cell-specific homeotic gene of Drosophila, encodes a putative transmembrane receptor with a tyrosine kinase domain. Science 236, 55–63
    OpenUrlAbstract/FREE Full Text
    1. Higashijima S.,
    2. Kojima T.,
    3. Michiue T.,
    4. Ishimaru S.,
    5. Emori Y.,
    6. Saigo K.
    (1992) Dual Bar homeo box genes of Drosophila required in two photoreceptor cells, R1 and R6, and primary pigment cells for normal eye development. Genes Dev 6, 50–60
    OpenUrlAbstract/FREE Full Text
    1. Hulskamp M.,
    2. Schröder C.,
    3. Pfeifle C.,
    4. Jäckle H.,
    5. Tautz D.
    (1989) Posterior segmentation of the Drosophila embryo in the absence of a maternal posterior organizer gene. Nature 338, 629–632
    OpenUrlCrossRefPubMed
    1. Irish V.,
    2. Lehmann R.,
    3. Akam M.
    (1989) The Drosophila posterior-group gene nanos functions by repressing hunchback activity. Nature 338, 646–648
    OpenUrlCrossRefPubMed
    1. Kalderon D.,
    2. Roberts B. L.,
    3. Richardson W. D.,
    4. Smith A. E.
    (1984) A short amino acid sequence able to specify nuclear location. Cell 39, 499–509
    OpenUrlCrossRefPubMedWeb of Science
    1. Karpilow J.,
    2. Kolodkin A.,
    3. Bork T.,
    4. Venkatesh T.
    (1989) Neuronal development in the Drosophila compound eye: rap gene function is required in photoreceptor cell R8 for ommatidial pattern formation. Genes Dev 3, 1834–1844
    OpenUrlAbstract/FREE Full Text
    1. Karr T. L.,
    2. Alberts B. M.
    (1986) Organization of the cytoskeleton in early Drosophila embryos. J. Cell Biol 102, 1494–1509
    OpenUrlAbstract/FREE Full Text
    1. Kim-Ha J.,
    2. Smith J. L.,
    3. Macdonald P. M.
    (1991) oskar mRNA is localized to the posterior pole of the Drosophila oocyte. Cell 66, 23–35
    OpenUrlCrossRefPubMedWeb of Science
    1. Kimmel B. E.,
    2. Heberlein U.,
    3. Rubin G. M.
    (1990) The homeodomain protein rough is expressed in a subset of cells in the developing Drosophila eye where it can specify photoreceptor cell subtype. Genes Dev 4, 712–727
    OpenUrlAbstract/FREE Full Text
    1. Klemenz R.,
    2. Weber U.,
    3. Gehring W. J.
    (1987) The white gene as a marker in a new P-element vector for gene transfer in Drosophila. Nucl. Acids Res 15, 3947–3959
    OpenUrlAbstract/FREE Full Text
    1. Landschulz W. H.,
    2. Johnson P. F.,
    3. McKnight S. L.
    (1988) The leucine zipper: A hypothetical structure common to a new class of DNA binding proteins. Science 240, 1759–1764
    OpenUrlAbstract/FREE Full Text
    1. Lasko P. F.,
    2. Ashburner M.
    (1988) The product of the Drosophila gene vasa is very similar to eukaryotic initiation factor-4A. Nature 335, 611–617
    OpenUrlCrossRefPubMedWeb of Science
    1. Lasko P. F.,
    2. Ashburner M.
    (1990) Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development. Genes Dev 4, 905–921
    OpenUrlAbstract/FREE Full Text
    1. Lehmann R.,
    2. Nusslein-Volhard C.
    (1987) Involvement of the pumilio gene in the transport of an abdominal signal in the Drosophila embryo. Nature 329, 167–170
    OpenUrlCrossRef
    1. Lehmann R.,
    2. Nusslein-Volhard C.
    (1991) The maternal gene nanos has a central role in posterior pattern formation of the Drosophila embryo. Development 112, 679–691
    OpenUrlAbstract
    1. Macdonald P. M.
    (1992) The Drosophila pumilio gene: an unusually long transcription unit and an unusual protein. Development 114, 221–232
    OpenUrlAbstract
    1. Manseau L. J.,
    2. Schupbach T.
    (1989) cappuccino and spire: two unique maternal-effect loci required for both the anteroposterior and dorsoventral patterns of the Drosophila embryo. Genes Dev 3, 1437–1452
    OpenUrlAbstract/FREE Full Text
    1. Mlodzik M.,
    2. Hiromi Y.,
    3. Weber U.,
    4. Goodman C.,
    5. Rubin G. M.
    (1990) The Drosophila seven-up gene, a member of the steroid receptor gene superfamily controls photoreceptor cell fates. Cell 60, 211–224
    OpenUrlCrossRefPubMedWeb of Science
    1. Moses K.,
    2. Ellis M. C.,
    3. Rubin G. M.
    (1989) The glass gene encodes a zinc-finger protein required by Drosophila photoreceptor cells. Nature 340, 531–536
    OpenUrlCrossRefPubMed
    1. Raff J. W.,
    2. Whitfield W. G. F.,
    3. Glover D. M.
    (1990) Two distinct mechanisms localise cyclin B transcripts in syncytial Drosophila embryos. Development 110, 1249–1261
    OpenUrlAbstract/FREE Full Text
    1. Ready D. F.,
    2. Hanson T. E.,
    3. Benzer S.
    (1976) Development of the Drosophila retina, a neurocrystalline lattice. Dev. Biol 53, 217–240
    OpenUrlCrossRefPubMedWeb of Science
    1. Reinke R.,
    2. Zipursky S. L.
    (1988) Cell-cell interaction in the Drosophila retina: the bride-of-sevenless gene is required in photoreceptor cell R8 for R7 cell development. Cell 55, 321–330
    OpenUrlCrossRefPubMedWeb of Science
    1. Rogers S.,
    2. Wells R.,
    3. Rechsteiner M.
    (1986) Amino acid sequences common to rapidly degraded proteins: the PEST hypothesis. Science 234, 364–368
    OpenUrlAbstract/FREE Full Text
    1. Schupbach T.,
    2. Wieschaus E.
    (1989). Female sterile mutations on the second chromosome of Drosophila melanogaster. I. Maternal effect mutations. Genetics 121, 101–117
    OpenUrlAbstract/FREE Full Text
    1. St. Johnston D.,
    2. Beuchle D.,
    3. Nusslein-Volhard C.
    (1991) staufen, a gene required to localize maternal RNAs in the Drosophila egg. Cell 66, 51–63
    OpenUrlCrossRefPubMedWeb of Science
    1. St. Johnston D.,
    2. Nusslein-Volhard C.
    (1992) The origin of pattern and polarity in the Drosophila embryo. Cell 68, 201–219
    OpenUrlCrossRefPubMedWeb of Science
    1. Struhl G.
    (1989) Differing strategies for organizing anterior and posterior body pattern in Drosophila embryos. Nature 338, 741–744
    OpenUrlCrossRefPubMed
    1. Tautz D.
    (1988) Regulation of the Drosophila segmentation gene hunchback by two maternal morphogenetic centers. Nature 332, 281–284
    OpenUrlCrossRefPubMed
    1. Thummel C. S.,
    2. Boulet A. M.,
    3. Lipshitz H. D.
    (1988) Vecotrs for Drosophila P element-mediated transformation and tissue culture transformation. Gene 74, 445–456
    OpenUrlCrossRefPubMedWeb of Science
    1. Tomlinson A.,
    2. Ready D. F.
    (1987) Neuronal differentiation in the Drosophila ommatidium. Dev. Biol 120, 366–376
    OpenUrlCrossRefPubMedWeb of Science
    1. Tomlinson A.,
    2. Ready D. F.
    (1987) Cell fate in the Drosophila ommatidium. Dev. Biol 123, 264–275
    OpenUrlCrossRefPubMedWeb of Science
    1. Tomlinson A.,
    2. Kimmel B. E.,
    3. Rubin G. M.
    (1988) rough, a Drosophila homeobox gene required in photoreceptors R2 and R5 for inductive interactions in the developing eye. Cell 55, 771–784
    OpenUrlCrossRefPubMedWeb of Science
    1. Wolff T.,
    2. Ready D. F.
    (1991) The beginning of pattern formation in the Drosophila compound eye: the morphogenetic furrow and the second mitotic wave. Development 113, 841–850
    OpenUrlAbstract
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JOURNAL ARTICLES
The fat facets gene is required for Drosophila eye and embryo development
J.A. Fischer-Vize, G.M. Rubin, R. Lehmann
Development 1992 116: 985-1000;
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JOURNAL ARTICLES
The fat facets gene is required for Drosophila eye and embryo development
J.A. Fischer-Vize, G.M. Rubin, R. Lehmann
Development 1992 116: 985-1000;

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