CCAAT/Enhancer-Binding Protein Beta Controls Differentiation-Specific Expression of Chromatin Remodeling Factor BRM

被引:0
|
作者
Itoh, Toshinari [1 ]
Miyake, Katsuhide [1 ]
Iijima, Shinji [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Biotechnol, Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词
SWI/SNF; neural cell differentiation; C/EBP beta; SWI-SNF COMPLEX; TRANSCRIPTIONAL REGULATION; SACCHAROMYCES-CEREVISIAE; GLUCOCORTICOID-RECEPTOR; RETINOBLASTOMA PROTEIN; ESTROGEN-RECEPTOR; SWI/SNF COMPLEX; HUMAN HOMOLOGS; BRG1; COMPLEX; ACTIVATION;
D O I
10.1007/978-1-4020-9646-4_32
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The chromatin remodeling complex, SWI/SNF exclusively contains BRG1 or BRM as an ATPase subunit. So far, we have confirmed that the expression of BRM was very low in neural precursor cells and fetal liver cells, and induced to a high level in terminally differentiated neurons and astrocytes, and adult liver cells. The expression of BRM was very low in undifferentiated P 19 cells and was induced to a high level during differentiation, In contrast, BRG1 was constantly expressed throughout differentiation. In this study, we analyzed developmental regulation of the brm gene. Luciferase reporter assays showed an increase in the transcriptional activity of the BRM promoter during differentiation of P19 cells. The promoter region of the brm gene contains two putative binding sites For CCAAT/enhancerbinding protein beta (C/EBP beta). Luciferase reporter assays showed that the binding of transcription factors C/EBP beta might Stimulate the transcriptional activity 4 the BRM promoter.
引用
收藏
页码:203 / 209
页数:7
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