Literature DB >> 7750635

The Drosophila toll gene functions zygotically and is necessary for proper motoneuron and muscle development.

M S Halfon1, C Hashimoto, H Keshishian.   

Abstract

Toll is a maternally required Drosophila gene that encodes a transmembrane protein with an important function in embryonic dorsal-ventral patterning. The Toll protein is widely expressed zygotically, but its roles in late embryo-genesis have not been described in detail. We have examined the expression of Toll protein in the late embryonic central nervous system and somatic musculature. Toll is expressed in a dynamic pattern in teh musculature, initially in several muscle fibers in each hemisegment, with a later narrowing of expression to a single muscle fiber pair. Zygotic Toll mutants were used to investigate the development consequences of loss of Toll expression. We found that loss of one or both copies of the Toll gene leads to widespread defects in motoneuron number and muscle patterning. Loss of motoneurons prevents certain muscle fibers from receiving their wild-type innervation. Denervation in the mutants results in collateral sprouting from nearby nerve branches and leads to the appearance of ectopically placed motor endings. The limited expressivity observed suggests that Toll is only one of several genes required for proper motoneuron and muscle specification.

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Year:  1995        PMID: 7750635     DOI: 10.1006/dbio.1995.1134

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  30 in total

1.  Drosophila Tey represses transcription of the repulsive cue Toll and generates neuromuscular target specificity.

Authors:  Mikiko Inaki; Makiko Shinza-Kameda; Afshan Ismat; Manfred Frasch; Akinao Nose
Journal:  Development       Date:  2010-05-26       Impact factor: 6.868

2.  The 18-wheeler mutation reveals complex antibacterial gene regulation in Drosophila host defense.

Authors:  M J Williams; A Rodriguez; D A Kimbrell; E D Eldon
Journal:  EMBO J       Date:  1997-10-15       Impact factor: 11.598

3.  Melanotic mutants in Drosophila: pathways and phenotypes.

Authors:  Svetlana Minakhina; Ruth Steward
Journal:  Genetics       Date:  2006-07-02       Impact factor: 4.562

4.  Mutation of TweedleD, a member of an unconventional cuticle protein family, alters body shape in Drosophila.

Authors:  Xiao Guan; Brooke W Middlebrooks; Sherry Alexander; Steven A Wasserman
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-30       Impact factor: 11.205

5.  A gain-of-function screen for genes that influence axon guidance identifies the NF-kappaB protein dorsal and reveals a requirement for the kinase Pelle in Drosophila photoreceptor axon targeting.

Authors:  Elizabeth N Mindorff; David D O'Keefe; Alain Labbé; Jennie Ping Yang; Yimiao Ou; Shingo Yoshikawa; Donald J van Meyel
Journal:  Genetics       Date:  2007-07-01       Impact factor: 4.562

6.  Laser ablation of Drosophila embryonic motoneurons causes ectopic innervation of target muscle fibers.

Authors:  T N Chang; H Keshishian
Journal:  J Neurosci       Date:  1996-09-15       Impact factor: 6.167

7.  A mosaic analysis in Drosophila fat body cells of the control of antimicrobial peptide genes by the Rel proteins Dorsal and DIF.

Authors:  P Manfruelli; J M Reichhart; R Steward; J A Hoffmann; B Lemaitre
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

8.  Toll-like receptor 3 is a potent negative regulator of axonal growth in mammals.

Authors:  Jill S Cameron; Lena Alexopoulou; Jacob A Sloane; Allitia B DiBernardo; Yinghua Ma; Bela Kosaras; Richard Flavell; Stephen M Strittmatter; Joseph Volpe; Richard Sidman; Timothy Vartanian
Journal:  J Neurosci       Date:  2007-11-21       Impact factor: 6.167

9.  NF-kappaB, IkappaB, and IRAK control glutamate receptor density at the Drosophila NMJ.

Authors:  Elizabeth S Heckscher; Richard D Fetter; Kurt W Marek; Stephanie D Albin; Graeme W Davis
Journal:  Neuron       Date:  2007-09-20       Impact factor: 17.173

10.  18 wheeler regulates apical constriction of salivary gland cells via the Rho-GTPase-signaling pathway.

Authors:  Tereza Kolesnikov; Steven K Beckendorf
Journal:  Dev Biol       Date:  2007-04-20       Impact factor: 3.582

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