Literature DB >> 9409675

A novel alpha integrin subunit associates with betaPS and functions in tissue morphogenesis and movement during Drosophila development.

K A Stark1, G H Yee, C E Roote, E L Williams, S Zusman, R O Hynes.   

Abstract

We have identified a novel alpha integrin subunit in Drosophila, that associates with betaPS integrin. We report the temporal expression of the gene encoding this integrin subunit, which we have called alphaPS3, throughout development and the localization of its expression during embryogenesis. AlphaPS3 RNA was localized to tissues undergoing invagination, tissue movement and morphogenesis such as salivary gland, trachea, midgut, dorsal vessel, midline of the ventral nerve cord, amnioserosa and the amnioproctodeal invagination. AlphaPS3 DNA localized to the chromosomal vicinity of scab (scb), previously identified by a failure of dorsal closure. Embryos homozygous for the 119 allele of scb had no detectable alphaPS3 RNA and the 1035 allele of scb contains a P element inserted just 5' of the coding region for the shorter of the gene's two transcripts. Furthermore, mutations in the scb locus exhibit additional defects corresponding to sites of alphaPS3 transcription, including abnormal salivary glands, mislocalization of the pericardial cells and interrupted trachea. Removal of both maternal and zygotic betaPS produced similar defects, indicating that these two integrin subunits associate in vivo and function in the movement and morphogenesis of tissues during development in Drosophila. Phenotypic similarities suggest that laminin A is a potential ligand for this integrin, at least in some tissues.

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Year:  1997        PMID: 9409675     DOI: 10.1242/dev.124.22.4583

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  55 in total

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3.  Uncoupling integrin adhesion and signaling: the betaPS cytoplasmic domain is sufficient to regulate gene expression in the Drosophila embryo.

Authors:  M D Martin-Bermudo; N H Brown
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Review 4.  The evolution of cell adhesion.

Authors:  R O Hynes; Q Zhao
Journal:  J Cell Biol       Date:  2000-07-24       Impact factor: 10.539

5.  Retraction of the Drosophila germ band requires cell-matrix interaction.

Authors:  Frieder Schöck; Norbert Perrimon
Journal:  Genes Dev       Date:  2003-03-01       Impact factor: 11.361

6.  Drosophila morphogenesis: tissue force laws and the modeling of dorsal closure.

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7.  Upregulation of forces and morphogenic asymmetries in dorsal closure during Drosophila development.

Authors:  X G Peralta; Y Toyama; M S Hutson; R Montague; S Venakides; D P Kiehart; G S Edwards
Journal:  Biophys J       Date:  2007-01-11       Impact factor: 4.033

8.  Genetic interaction between integrins and moleskin, a gene encoding a Drosophila homolog of importin-7.

Authors:  Scott E Baker; James A Lorenzen; Steven W Miller; Thomas A Bunch; Alison L Jannuzi; Mark H Ginsberg; Lizabeth A Perkins; Danny L Brower
Journal:  Genetics       Date:  2002-09       Impact factor: 4.562

9.  Drosophila laminins act as key regulators of basement membrane assembly and morphogenesis.

Authors:  Jose M Urbano; Catherine N Torgler; Cristina Molnar; Ulrich Tepass; Ana López-Varea; Nicholas H Brown; Jose F de Celis; Maria D Martín-Bermudo
Journal:  Development       Date:  2009-11-11       Impact factor: 6.868

10.  Integrin αPS3/βν-mediated phagocytosis of apoptotic cells and bacteria in Drosophila.

Authors:  Saori Nonaka; Kaz Nagaosa; Toshinobu Mori; Akiko Shiratsuchi; Yoshinobu Nakanishi
Journal:  J Biol Chem       Date:  2013-02-20       Impact factor: 5.157

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