Literature DB >> 3209069

A group of genes required for pattern formation in the ventral ectoderm of the Drosophila embryo.

U Mayer1, C Nüsslein-Volhard.   

Abstract

Mutations in the genes spitz (spi), Star (S), single-minded (sim), pointed (pnt), rhomboid (rho) (all zygotic), and sichel (sic) (maternal), collectively called the spitz group, cause similar pattern alterations in ventral ectodermal derivatives of the Drosophila embryo. The cuticle structures lacking in mutant embryos normally derive from longitudinal strips of the ventro-lateral blastoderm. Defects were found in the median part of the central nervous system in whole-mount embryos stained with anti-HRP (horseradish peroxidase) antibodies. In addition, the nerve cells expressing the even-skipped protein appeared abnormally arranged. These results suggest that groups of cells from the same region, including both epidermal and neural precursor cells, require spitz-group gene activity for normal development. The members of the spitz group differ from one another: sim affects a more median strip of the ventral ectoderm than the other zygotic genes and pnt causes separation rather than deletion of pattern elements. As shown by pole cell transplantations, spi and S are also required for normal development of the female germ line, while sim, rho, and pnt appear to be exclusively zygotically expressed, and the maternal gene sic acts in the germ line autonomously. Some embryos produced by sic-homozygous females differentiate the spitz phenotype, others develop normally or die early. Of all the spitz-group genes, sim appears to have the most specific effect on the embryonic pattern. The significance of the spitz-group phenotypes for the dorso-ventral pattern formation is discussed.

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Mesh:

Year:  1988        PMID: 3209069     DOI: 10.1101/gad.2.11.1496

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


  52 in total

1.  Expression in mammalian cell cultures reveals interdependent, but distinct, functions for Star and Rhomboid proteins in the processing of the Drosophila transforming-growth-factor-alpha homologue Spitz.

Authors:  John C Pascall; Jane E Luck; Kenneth D Brown
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2.  A fly's eye view of EGF receptor signalling.

Authors:  Matthew Freeman
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3.  Isolation of mutations in the Drosophila homologues of the human Neurofibromatosis 2 and yeast CDC42 genes using a simple and efficient reverse-genetic method.

Authors:  R G Fehon; T Oren; D R LaJeunesse; T E Melby; B M McCartney
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4.  Requirement for cell-proliferation control genes in Drosophila oogenesis.

Authors:  J Szabad; V A Jursnich; P J Bryant
Journal:  Genetics       Date:  1991-03       Impact factor: 4.562

5.  Non-cell-autonomous control of denticle diversity in the Drosophila embryo.

Authors:  Stacie A Dilks; Stephen DiNardo
Journal:  Development       Date:  2010-04       Impact factor: 6.868

6.  Functional and evolutionary implications of enhanced genomic analysis of rhomboid intramembrane proteases.

Authors:  Marius K Lemberg; Matthew Freeman
Journal:  Genome Res       Date:  2007-10-15       Impact factor: 9.043

Review 7.  How intramembrane proteases bury hydrolytic reactions in the membrane.

Authors:  Elinor Erez; Deborah Fass; Eitan Bibi
Journal:  Nature       Date:  2009-05-21       Impact factor: 49.962

8.  Dynamics of the rhomboid-like protein RHBDD2 expression in mouse retina and involvement of its human ortholog in retinitis pigmentosa.

Authors:  Novruz B Ahmedli; Yekaterina Gribanova; Collins C Njoku; Akash Naidu; Alejandra Young; Emmanuel Mendoza; Clyde K Yamashita; Riza Köksal Ozgül; Jerry E Johnson; Donald A Fox; Debora B Farber
Journal:  J Biol Chem       Date:  2013-02-05       Impact factor: 5.157

9.  Keren, a new ligand of the Drosophila epidermal growth factor receptor, undergoes two modes of cleavage.

Authors:  Aderet Reich; Ben-Zion Shilo
Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

10.  Germ line and embryonic expression of Fex, a member of the Drosophila F-element retrotransposon family, is mediated by an internal cis-regulatory control region.

Authors:  B Kerber; S Fellert; H Taubert; M Hoch
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

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