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多个同源结构域锌指转录因子ATBF1的亚型对C2C12细胞成肌分化的正负调控

Positive and negative regulation of myogenic differentiation of C2C12 cells by isoforms of the multiple homeodomain zinc finger transcription factor ATBF1.

作者信息

Berry F B, Miura Y, Mihara K, Kaspar P, Sakata N, Hashimoto-Tamaoki T, Tamaoki T

机构信息

Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta T2N 4N1, Canada.

出版信息

J Biol Chem. 2001 Jul 6;276(27):25057-65. doi: 10.1074/jbc.M010378200. Epub 2001 Apr 18.

Abstract

The ATBF1 gene encodes two protein isoforms, the 404-kDa ATBF1-A, possessing four homeodomains and 23 zinc fingers, and the 306-kDa ATBF1-B, lacking a 920-amino acid N-terminal region of ATBF1-A which contains 5 zinc fingers. In vitro, ATBF1-A was expressed in proliferating C2C12 myoblasts, but its expression levels decreased upon induction of myogenic differentiation in low serum medium. Forced expression of ATBF1-A in C2C12 cells resulted in repression of MyoD and myogenin expression and elevation of Id3 and cyclin D1 expression, leading to inhibition of myogenic differentiation in low serum. In contrast, transfection of C2C12 cells with the ATBF1-B isoform led to an acceleration of myogenic differentiation, as indicated by an earlier onset of myosin heavy chain expression and formation of a higher percentage of multinucleated myotubes. The fourth homeodomain of ATBF1-A bound to an AT-rich element adjacent to the E1 E-box of the muscle regulatory factor 4 promoter mediating transcriptional repression. The ATBF1-A-specific N-terminal region possesses general transcription repressor activity. These results suggest that ATBF1-A plays a role in the maintenance of the undifferentiated myoblast state, and its down-regulation is a prerequisite to initiate terminal differentiation of C2C12 cells.

摘要

ATBF1基因编码两种蛋白质异构体,即404 kDa的ATBF1-A,它具有四个同源结构域和23个锌指;以及306 kDa的ATBF1-B,它缺少ATBF1-A的一个包含5个锌指的920个氨基酸的N端区域。在体外,ATBF1-A在增殖的C2C12成肌细胞中表达,但在低血清培养基中诱导肌源性分化时其表达水平下降。在C2C12细胞中强制表达ATBF1-A导致MyoD和肌细胞生成素表达受到抑制,Id3和细胞周期蛋白D1表达升高,从而在低血清中抑制肌源性分化。相反,用ATBF1-B异构体转染C2C12细胞导致肌源性分化加速,这表现为肌球蛋白重链表达提前开始以及多核肌管形成的百分比更高。ATBF1-A的第四个同源结构域与肌肉调节因子4启动子的E1 E盒相邻的富含AT的元件结合,介导转录抑制。ATBF1-A特异性的N端区域具有一般转录抑制活性。这些结果表明,ATBF1-A在维持未分化的成肌细胞状态中起作用,其下调是启动C2C12细胞终末分化的先决条件。

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