Literature DB >> 17462629

Involvement of BTBD1 in mesenchymal differentiation.

Didier F Pisani1, Anne-Sophie Coldefy, Christian Elabd, Candice Cabane, Jerome Salles, Martine Le Cunff, Benoit Derijard, Ez-Zoubir Amri, Christian Dani, Jean J Leger, Claude A Dechesne.   

Abstract

BTBD1 is a recently cloned BTB-domain-containing protein particularly expressed in skeletal muscle and interacting with DNA topoisomerase 1 (Topo1), a key enzyme of cell survival. We have previously demonstrated that stable overexpression of a N-terminal truncated BTBD1 inhibited ex vivo myogenesis but not adipogenesis of pluripotent C2C12 cells. Here, BTBD1 expression was studied in three models of cellular differentiation: myogenesis (C2C12 cells), adipogenesis (3T3-L1 cells) and osteogenesis (hMADS cells). BTBD1 mRNA was found to be upregulated during myogenesis. At the opposite, we have not observed BTBD1 upregulation in an altered myogenesis cellular model and we observed a downregulation of BTBD1 mRNA expression in adipogenesis. Interestingly, amounts of Topo1 protein, but not Topo1 mRNA, were found to be modulated at the opposite of BTBD1 mRNA. No variation of BTBD1 expression was measured during osteogenesis. Taken together, these results indicate that BTBD1 mRNA is specifically regulated during myogenic and adipogenic differentiation, in relation with Topo1 expression. Moreover, they corroborate observations made previously with truncated BTBD1 and show that BTBD1 is a key protein of balance between adipogenesis and myogenesis. Finally, a transcriptome analysis gave molecular clues to decipher BTBD1 role, with an emphasis on the involvement in ubiquitin/proteasome degradation pathway.

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Year:  2007        PMID: 17462629     DOI: 10.1016/j.yexcr.2007.03.030

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  4 in total

1.  Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia.

Authors:  Margaret J Wat; Victoria B Enciso; Wojciech Wiszniewski; Trevor Resnick; Patricia Bader; Elizabeth R Roeder; Debra Freedenberg; Chester Brown; Pawel Stankiewicz; Sau-Wai Cheung; Daryl A Scott
Journal:  J Med Genet       Date:  2010-10-04       Impact factor: 6.318

2.  Molecular signature of mineralocorticoid receptor signaling in cardiomyocytes: from cultured cells to mouse heart.

Authors:  Celine Latouche; Yannis Sainte-Marie; Marja Steenman; Paulo Castro Chaves; Aniko Naray-Fejes-Toth; Geza Fejes-Toth; Nicolette Farman; Frederic Jaisser
Journal:  Endocrinology       Date:  2010-06-30       Impact factor: 4.736

3.  Establishment and Verification of a Gene Signature for Diagnosing Type 2 Diabetics by WGCNA, LASSO Analysis, and In Vitro Experiments.

Authors:  Huaming Shao; Yong Zhang; Yishuai Liu; Yan Yang; Xiaozhu Tang; Jiajia Li; Changxin Jia
Journal:  Biomed Res Int       Date:  2022-05-23       Impact factor: 3.246

Review 4.  The Role of Cullin-RING Ligases in Striated Muscle Development, Function, and Disease.

Authors:  Jordan Blondelle; Andrea Biju; Stephan Lange
Journal:  Int J Mol Sci       Date:  2020-10-26       Impact factor: 5.923

  4 in total

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