YY2 Promotes Osteoblast Differentiation by Upregulating Osterix Transcriptional Activity

Yin Yang 2 (YY2) is a paralog of YY1, a well-known multifunctional transcription factor containing a C-terminal zinc finger domain. Although the role of YY1 in various biological processes, such as the cell cycle, cell differentiation and tissue development, is well established, the function of YY2...

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Bibliographic Details
Main Authors: Kim, H.S (Author), Kim, M.J (Author), Lee, K.Y (Author), Lee, S.H (Author), Piao, M. (Author)
Format: Article
Language:English
Published: MDPI 2022
Subjects:
YY2
Online Access:View Fulltext in Publisher
LEADER 02128nam a2200217Ia 4500
001 10-3390-ijms23084303
008 220425s2022 CNT 000 0 und d
020 |a 16616596 (ISSN) 
245 1 0 |a YY2 Promotes Osteoblast Differentiation by Upregulating Osterix Transcriptional Activity 
260 0 |b MDPI  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3390/ijms23084303 
520 3 |a Yin Yang 2 (YY2) is a paralog of YY1, a well-known multifunctional transcription factor containing a C-terminal zinc finger domain. Although the role of YY1 in various biological processes, such as the cell cycle, cell differentiation and tissue development, is well established, the function of YY2 has not been fully determined. In this study, we investigated the functional role of YY2 during osteoblast differentiation. YY2 overexpression and knockdown increased and decreased osteoblast differentiation, respectively, in BMP4-induced C2C12 cells. Mechanistically, YY2 overexpression increased the mRNA and protein levels of Osterix (Osx), whereas YY2 knockdown had the opposite effect. To investigate whether YY2 regulates Osx transcription, the effect of YY2 overexpression and knockdown on Osx promoter activity was evaluated. YY2 overexpression significantly increased Osx promoter activity in a dose-dependent manner, whereas YY2 knockdown had the opposite effect. Furthermore, vectors containing deletion and point mutations were constructed to specify the regulation site. Both the Y1 and Y2 sites were responsible for YY2-mediated Osx promoter activation. These results indicate that YY2 is a positive regulator of osteoblast differentiation that functions by upregulating the promoter activity of Osx, a representative osteogenic transcription factor in C2C12 cells. © 2022 by the authors. Licensee MDPI, Basel, Switzerland. 
650 0 4 |a osteoblast differentiation 
650 0 4 |a Osterix 
650 0 4 |a YY2 
700 1 |a Kim, H.S.  |e author 
700 1 |a Kim, M.J.  |e author 
700 1 |a Lee, K.Y.  |e author 
700 1 |a Lee, S.H.  |e author 
700 1 |a Piao, M.  |e author 
773 |t International Journal of Molecular Sciences