Literature DB >> 2514120

cappuccino and spire: two unique maternal-effect loci required for both the anteroposterior and dorsoventral patterns of the Drosophila embryo.

L J Manseau1, T Schüpbach.   

Abstract

cappuccino and spire are unique Drosophila maternal-effect loci that participate in pattern formation in both the anteroposterior and dorsoventral axes of the early embryo. Mutant females produce embryos lacking pole cells, polar granules, and normal abdominal segmentation. They share these defects with the posterior group of maternal-effect genes. Although embryos are defective in abdominal segmentation, in double mutant combinations with Bicaudal D, abdominal segments can be formed in the anterior half of the egg. This indicates that embryos produced by mutant females contain the 'posterior determinant' required for abdominal segmentation (Nüsslein-Volhard et al. 1987) and suggests that the wild-type gene products are not required for production of the posterior determinant but, rather, for its localization or stabilization. The vasa protein, a component of polar granules, is not localized at the posterior pole of mutant egg chambers or embryos, providing additional support for the hypothesis that localization to or stabilization of substances at the posterior pole of the egg chamber is defective in mutant females. Females mutant for the strongest alleles also produce dorsalized embryos. Phenotypic analysis reveals that these dorsalized embryos also have abdominal segmentation defects. The mutant phenotypes can be ordered in a series of increasing severity. Pole cell formation is most sensitive to loss of functional gene products, followed by abdominal segmentation, whereas normal dorsoventral patterning is the least sensitive to loss of functional gene products. In addition, mutant females contain egg chambers that appear to be dorsalized, resulting in the production of eggs with dorsalized eggshells. Germ-line mosaics indicate that cappuccino and spire are required in the oocyte-nurse cell complex. This suggests that the eggshell phenotype results from altered pattern in the underlying germ cell. Also, we defined the epistatic relationships between several early patterning loci, on the basis of an analysis of the eggs and embryos produced by females doubly mutant for cappuccino or spire and other loci that affect the pattern of both the egg and the embryo. On the basis of our current knowledge of the genes involved in this process, we formulated a working model for the early steps in dorsoventral patterning.

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Year:  1989        PMID: 2514120     DOI: 10.1101/gad.3.9.1437

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  56 in total

1.  Map position and expression of the genes in the 38 region of Drosophila.

Authors:  H Butler; S Levine; X Wang; S Bonyadi; G Fu; P Lasko; B Suter; R Doerig
Journal:  Genetics       Date:  2001-08       Impact factor: 4.562

2.  Ras1 interacts with multiple new signaling and cytoskeletal loci in Drosophila eggshell patterning and morphogenesis.

Authors:  J D Schnorr; R Holdcraft; B Chevalier; C A Berg
Journal:  Genetics       Date:  2001-10       Impact factor: 4.562

3.  Multiple forms of Spire-actin complexes and their functional consequences.

Authors:  Christine K Chen; Michael R Sawaya; Martin L Phillips; Emil Reisler; Margot E Quinlan
Journal:  J Biol Chem       Date:  2012-02-08       Impact factor: 5.157

4.  Structures of actin-bound Wiskott-Aldrich syndrome protein homology 2 (WH2) domains of Spire and the implication for filament nucleation.

Authors:  Anna M Ducka; Peteranne Joel; Grzegorz M Popowicz; Kathleen M Trybus; Michael Schleicher; Angelika A Noegel; Robert Huber; Tad A Holak; Tomasz Sitar
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-10       Impact factor: 11.205

Review 5.  Cell-cell communication and axis specification in the Drosophila oocyte.

Authors:  John S Poulton; Wu-Min Deng
Journal:  Dev Biol       Date:  2007-08-22       Impact factor: 3.582

6.  Coordinately and differentially mutable activities of torpedo, the Drosophila melanogaster homolog of the vertebrate EGF receptor gene.

Authors:  R J Clifford; T Schüpbach
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

7.  Genetic modifiers of abnormal organelle biogenesis in a Drosophila model of BLOC-1 deficiency.

Authors:  Verónica T Cheli; Richard W Daniels; Ruth Godoy; Diego J Hoyle; Vasundhara Kandachar; Marta Starcevic; Julian A Martinez-Agosto; Stephen Poole; Aaron DiAntonio; Vett K Lloyd; Henry C Chang; David E Krantz; Esteban C Dell'Angelica
Journal:  Hum Mol Genet       Date:  2009-12-16       Impact factor: 6.150

Review 8.  Formins in development: orchestrating body plan origami.

Authors:  Raymond Liu; Elena V Linardopoulou; Gregory E Osborn; Susan M Parkhurst
Journal:  Biochim Biophys Acta       Date:  2008-10-14

9.  Identification of a short Spir interaction sequence at the C-terminal end of formin subgroup proteins.

Authors:  Markos Pechlivanis; Annette Samol; Eugen Kerkhoff
Journal:  J Biol Chem       Date:  2009-07-15       Impact factor: 5.157

10.  MIM-B, a putative metastasis suppressor protein, binds to actin and to protein tyrosine phosphatase delta.

Authors:  Jacquelyn A Woodings; Stewart J Sharp; Laura M Machesky
Journal:  Biochem J       Date:  2003-04-15       Impact factor: 3.857

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