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

被引:50
作者
Ajima, Rieko [1 ]
Akazawa, Hiroshi [3 ]
Kodama, Maho [2 ]
Takeshita, Fumitaka [2 ]
Otsuka, Ayaka [1 ]
Kohno, Takashi [1 ]
Komuro, Issei [3 ]
Ochiya, Takahiro [2 ]
Yokota, Jun [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Biol, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Res Inst, Sect Studies Metastasis, Tokyo 1040045, Japan
[3] Chiba Univ, Grad Sch Med, Dept Cardiovasc Sci & Med, Chiba 2608677, Japan
基金
日本学术振兴会;
关键词
D O I
10.1111/j.1365-2443.2008.01226.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:987 / 999
页数:13
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