The topoisomerase 1-interacting protein BTBD1 is essential for muscle cell differentiation
Author(s) -
Didier F. Pisani,
Candice Cabane,
Benoı̂t Dérijard,
Claude A. Dechesne
Publication year - 2004
Publication title -
cell death and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.348
H-Index - 218
eISSN - 1476-5403
pISSN - 1350-9047
DOI - 10.1038/sj.cdd.4401479
Subject(s) - c2c12 , myocyte , cellular differentiation , microbiology and biotechnology , nuclear localization sequence , biology , skeletal muscle , myogenesis , nuclear protein , biochemistry , gene , transcription factor , endocrinology , nucleus
DNA topoisomerase I (Topo1) contributes to vital biological functions, but its regulation is not clearly understood. The BTBD1 protein was recently cloned on the basis of its interaction with the core domain of Topo1 and is expressed particularly in skeletal muscle. To determine BTBD1 functions in this tissue, the in vitro model used was the C2C12 mouse muscle cell line, which expresses BTBD1 mainly after myotube differentiation. We studied the effects of a stably overexpressed BTBD1 protein truncated of the 108 N-terminal amino-acid residues and harbouring a C-terminal FLAG tag (Delta-BTBD1). The proliferation speed of Delta-BTBD1 C2C12 cells was significantly decreased and no myogenic differentiation was observed, although these cells maintained their capacity to enter adipocyte differentiation. These alterations could be related to Topo1 deregulation. This hypothesis is further supported by the decrease in nuclear Topo1 content in Delta-BTBTD1 proliferative C2C12 cells and the switch from the main peripheral nuclear localization of Topo1 to a mainly nuclear diffuse localization in Delta-BTBTD1 C2C12 cells. Finally, this study demonstrated that BTBD1 is essential for myogenic differentiation.
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