Literature DB >> 9136009

The mup-4 locus in Caenorhabditis elegans is essential for hypodermal integrity, organismal morphogenesis and embryonic body wall muscle position.

B K Gatewood1, E A Bucher.   

Abstract

mup-4 is a member of a set of genes essential for correct embryonic body wall muscle cell positions in Caenorhabditis elegans. The mup-4 phenotype is variably expressed and three discrete arrest phenotypes arise during the phase of embryonic development when the worm elongates from a ball of cells to its worm shape (organismal morphogenesis). Mutants representing two of the phenotypic classes arrest without successful completion of elongation. Mutants of the third phenotypic class arrest after completion of elongation. Mutants that arrest after elongation display profound dorsal and ventral body wall muscle cell position abnormalities and a characteristic kinked body shape (the Mup phenotype) due to the muscle cell position abnormalities. Significantly, genetic mosaic analysis of mup-4 mutants demonstrates that mup-4 gene function is essential in the AB lineage, which generates most of the hypodermis (epidermis), a tissue with which muscle interacts. Consistent with the genetic mosaic data, phenotypic characterizations reveal that mutants have defects in hypodermal integrity and morphology. Our analyses support the conclusion that mup-4 is essential for hypodermal function and that this function is necessary for organismal morphogenesis and for the maintenance of body wall muscle position.

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Year:  1997        PMID: 9136009      PMCID: PMC1207934     

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


  34 in total

1.  Male Phenotypes and Mating Efficiency in CAENORHABDITIS ELEGANS.

Authors:  J Hodgkin
Journal:  Genetics       Date:  1983-01       Impact factor: 4.562

2.  The ncl-1 gene and genetic mosaics of Caenorhabditis elegans.

Authors:  E M Hedgecock; R K Herman
Journal:  Genetics       Date:  1995-11       Impact factor: 4.562

3.  Cell fusions in the developing epithelial of C. elegans.

Authors:  B Podbilewicz; J G White
Journal:  Dev Biol       Date:  1994-02       Impact factor: 3.582

4.  The generation and genetic analysis of suppressors of lethal mutations in the Caenorhabditis elegans rol-3(V) gene.

Authors:  W B Barbazuk; R C Johnsen; D L Baillie
Journal:  Genetics       Date:  1994-01       Impact factor: 4.562

5.  Developmental genetics of the mechanosensory neurons of Caenorhabditis elegans.

Authors:  M Chalfie; J Sulston
Journal:  Dev Biol       Date:  1981-03       Impact factor: 3.582

6.  Paramyosin gene (unc-15) of Caenorhabditis elegans. Molecular cloning, nucleotide sequence and models for thick filament structure.

Authors:  H Kagawa; K Gengyo; A D McLachlan; S Brenner; J Karn
Journal:  J Mol Biol       Date:  1989-05-20       Impact factor: 5.469

7.  The minor myosin heavy chain, mhcA, of Caenorhabditis elegans is necessary for the initiation of thick filament assembly.

Authors:  R H Waterston
Journal:  EMBO J       Date:  1989-11       Impact factor: 11.598

8.  Genes critical for muscle development and function in Caenorhabditis elegans identified through lethal mutations.

Authors:  B D Williams; R H Waterston
Journal:  J Cell Biol       Date:  1994-02       Impact factor: 10.539

9.  Assembly of body wall muscle and muscle cell attachment structures in Caenorhabditis elegans.

Authors:  M C Hresko; B D Williams; R H Waterston
Journal:  J Cell Biol       Date:  1994-02       Impact factor: 10.539

10.  Myosin and paramyosin of Caenorhabditis elegans embryos assemble into nascent structures distinct from thick filaments and multi-filament assemblages.

Authors:  H F Epstein; D L Casey; I Ortiz
Journal:  J Cell Biol       Date:  1993-08       Impact factor: 10.539

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  5 in total

1.  Expression profile of Caenorhabditis elegans mutant for the Werner syndrome gene ortholog reveals the impact of vitamin C on development to increase life span.

Authors:  Alexandra Dallaire; Sophie Proulx; Martin J Simard; Michel Lebel
Journal:  BMC Genomics       Date:  2014-10-27       Impact factor: 3.969

2.  Mutations affecting nerve attachment of Caenorhabditis elegans.

Authors:  G Shioi; M Shoji; M Nakamura; T Ishihara; I Katsura; H Fujisawa; S Takagi
Journal:  Genetics       Date:  2001-04       Impact factor: 4.562

3.  mua-3, a gene required for mechanical tissue integrity in Caenorhabditis elegans, encodes a novel transmembrane protein of epithelial attachment complexes.

Authors:  M Bercher; J Wahl; B E Vogel; C Lu; E M Hedgecock; D H Hall; J D Plenefisch
Journal:  J Cell Biol       Date:  2001-07-23       Impact factor: 10.539

4.  MUP-4 is a novel transmembrane protein with functions in epithelial cell adhesion in Caenorhabditis elegans.

Authors:  L Hong; T Elbl; J Ward; C Franzini-Armstrong; K K Rybicka; B K Gatewood; D L Baillie; E A Bucher
Journal:  J Cell Biol       Date:  2001-07-23       Impact factor: 10.539

5.  Ca2+-dependent muscle dysfunction caused by mutation of the Caenorhabditis elegans troponin T-1 gene.

Authors:  K McArdle; T S Allen; E A Bucher
Journal:  J Cell Biol       Date:  1998-11-30       Impact factor: 10.539

  5 in total

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