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Publication : Deficiency of Myo18B in mice results in embryonic lethality with cardiac myofibrillar aberrations.

First Author  Ajima R Year  2008
Journal  Genes Cells Volume  13
Issue  10 Pages  987-99
PubMed ID  18761673 Mgi Jnum  J:142442
Mgi Id  MGI:3821523 Doi  10.1111/j.1365-2443.2008.01226.x
Citation  Ajima R, et al. (2008) Deficiency of Myo18B in mice results in embryonic lethality with cardiac myofibrillar aberrations. Genes Cells 13(10):987-99
abstractText  Myo18B is an unconventional myosin family protein expressed predominantly in muscle cells. Although conventional myosins are known to be localized on the A-bands and function as a molecular motor for muscle contraction, Myo18B protein was localized on the Z-lines of myofibrils in striated muscles. Like Myo18A, another 18th class of myosin, the N-terminal unique domain of the protein and not the motor domain and the coiled-coil tail is critical for its localization to F-actin in myocytes. Myo18B expression was induced by myogenic differentiation through the binding of myocyte-specific enhancer factor-2 to its promoter. Deficiency of Myo18B caused an embryonic lethality in mice accompanied by disruption of myofibrillar structures in cardiac myocytes at embryonic day 10.5. Thus, Myo18B is a unique unconventional myosin that is predominantly expressed in myocytes and whose expression is essential for the development and/or maintenance of myofibrillar structure.
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