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Myosin-1a is critical for normal brush border structure and composition

  1. Author:
    Tyska, M. J.
    Mackey, A. T.
    Huang, J. D.
    Copeland, N. G.
    Jenkins, N. A.
    Mooseker, M. S.
  2. Author Address

    Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA. NCI, NIH, Ft Detrick, MD 21702 USA. Yale Univ, Dept Cell Biol, New Haven, CT 06520 USA. Yale Univ, Dept Pathol, New Haven, CT 06520 USA Tyska, MJ, Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
    1. Year: 2005
    2. Date: MAY
  1. Journal: Molecular Biology of the Cell
    1. 16
    2. 5
    3. Pages: 2443-2457
  2. Type of Article: Article
  1. Abstract:

    To develop our understanding of myosin-1a function in vivo, we have created a mouse line null for the myosin-la gene. Myosin-1a knockout mice demonstrate no overt phenotypes at the whole animal level but exhibit significant perturbations and signs of stress at the cellular level. Among these are defects in microvillar membrane morphology, distinct changes in brush-border organization, loss of numerous cytoskeletal and membrane components from the brush border, and redistribution of intermediate filament proteins into the brush border. We also observed significant ectopic recruitment of another short-tailed class I motor, myosin-1c, into the brush border of knockout enterocytes. This latter finding, a clear demonstration of functional redundancy among vertebrate myosins-I, may account for the lack of a whole animal phenotype. Nevertheless, these results indicate that myosin-1a is a critical multifunctional component of the enterocyte, required for maintaining the normal composition and highly ordered structure of the brush border

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External Sources

  1. WOS: 000228737400026

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