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Expression of a transfected mouse muscle-creatine kinase gene is induced upon growth factor deprivation of myogenic but not of nonmyogenic cells.

作者信息

Johnson J E, Gartside C L, Jaynes J B, Hauschka S D

机构信息

Department of Biochemistry, University of Washington, Seattle 98195.

出版信息

Dev Biol. 1989 Jul;134(1):258-62. doi: 10.1016/0012-1606(89)90095-x.

DOI:10.1016/0012-1606(89)90095-x
PMID:2731652
Abstract

To determine whether mitogen-regulated expression of skeletal muscle genes is independent of cell type, muscle and nonmuscle cells were transfected with cloned 5'-flanking sequences of muscle creatine kinase (MCK) fused to a heterologous reporter gene and tested for expression in high and low mitogen culture conditions. Consistent with the behavior of endogenous MCK, a -3300MCK-CAT gene is expressed at high levels in differentiated muscle cells but at low to undetectable levels in proliferating myoblasts and in either mitogen-deprived or stimulated nonmuscle cells of mesodermal, ectodermal, or endodermal origin. A -776MCK-CAT gene behaves similarly with respect to its cell type specificity but it supports only an intermediate expression level in response to mitogen deprivation in skeletal muscle cells. These data suggest that the -3300 to +7 nucleotide region of mouse MCK contains one or more elements which are activable by mitogen deprivation only in myogenic cells.

摘要

相似文献

1
Expression of a transfected mouse muscle-creatine kinase gene is induced upon growth factor deprivation of myogenic but not of nonmyogenic cells.
Dev Biol. 1989 Jul;134(1):258-62. doi: 10.1016/0012-1606(89)90095-x.
2
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引用本文的文献

1
Differentiation and fiber type-specific activity of a muscle creatine kinase intronic enhancer.肌酸激酶内含子增强子的分化和纤维类型特异性活性。
Skelet Muscle. 2011 Jul 7;1:25. doi: 10.1186/2044-5040-1-25.
2
Multiple regulatory elements contribute differentially to muscle creatine kinase enhancer activity in skeletal and cardiac muscle.多种调控元件对骨骼肌和心肌中肌酸激酶增强子活性的贡献各不相同。
Mol Cell Biol. 1993 May;13(5):2753-64. doi: 10.1128/mcb.13.5.2753-2764.1993.