Literature DB >> 10353905

Genetic analysis of the bone morphogenetic protein-related gene, gbb, identifies multiple requirements during Drosophila development.

K A Wharton1, J M Cook, S Torres-Schumann, K de Castro, E Borod, D A Phillips.   

Abstract

We have isolated mutations in the Drosophila melanogaster gene glass bottom boat (gbb), which encodes a TGF-beta signaling molecule (formerly referred to as 60A) with highest sequence similarity to members of the bone morphogenetic protein (BMP) subgroup including vertebrate BMPs 5-8. Genetic analysis of both null and hypomorphic gbb alleles indicates that the gene is required in many developmental processes, including embryonic midgut morphogenesis, patterning of the larval cuticle, fat body morphology, and development and patterning of the imaginal discs. In the embryonic midgut, we show that gbb is required for the formation of the anterior constriction and for maintenance of the homeotic gene Antennapedia in the visceral mesoderm. In addition, we show a requirement for gbb in the anterior and posterior cells of the underlying endoderm and in the formation and extension of the gastric caecae. gbb is required in all the imaginal discs for proper disc growth and for specification of veins in the wing and of macrochaete in the notum. Significantly, some of these tissues have been shown to also require the Drosophila BMP2/4 homolog decapentaplegic (dpp), while others do not. These results indicate that signaling by both gbb and dpp may contribute to the development of some tissues, while in others, gbb may signal independently of dpp.

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Year:  1999        PMID: 10353905      PMCID: PMC1460618     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  48 in total

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Authors:  J F de Celis
Journal:  Development       Date:  1997-03       Impact factor: 6.868

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Authors:  F Thüringer; S M Cohen; M Bienz
Journal:  EMBO J       Date:  1993-06       Impact factor: 11.598

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8.  Medea is a Drosophila Smad4 homolog that is differentially required to potentiate DPP responses.

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9.  The Drosophila Medea gene is required downstream of dpp and encodes a functional homolog of human Smad4.

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Journal:  Development       Date:  1998-04       Impact factor: 6.868

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  39 in total

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Review 6.  TGF-β Family Signaling in Drosophila.

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Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

Review 8.  Cross-talk between nitric oxide and transforming growth factor-beta1 in malaria.

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9.  Synaptic strengthening mediated by bone morphogenetic protein-dependent retrograde signaling in the Drosophila CNS.

Authors:  Richard A Baines
Journal:  J Neurosci       Date:  2004-08-04       Impact factor: 6.167

10.  Molecular mechanisms that enhance synapse stability despite persistent disruption of the spectrin/ankyrin/microtubule cytoskeleton.

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