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Induction of Id2 expression by cardiac transcription factors GATA4 and Nkx2.5

Authors
Lim, Joong-YeonKim, Won HoKim, JoonPark, Sang Ick
Issue Date
1-1월-2008
Publisher
WILEY-LISS
Keywords
Idb2 protein; cell differentiation; transcription factors; myocytes; gene expression regulation
Citation
JOURNAL OF CELLULAR BIOCHEMISTRY, v.103, no.1, pp.182 - 194
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CELLULAR BIOCHEMISTRY
Volume
103
Number
1
Start Page
182
End Page
194
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/124453
DOI
10.1002/jcb.21396
ISSN
0730-2312
Abstract
Inhibitor of differentiation/DNA binding (Id) proteins function as a regulator of helix-loop-helix proteins participating in cell lineage commitment and differentiation. Here, we observed a marked induction of Id2 during cardiomyocyte differentiation from P19CL6 murine embryonic teratocarcinoma stem cells, prompting us to investigate the upstream regulatory mechanism of Id2 induction. Computer analysis of Id2 promoter and subsequent electrophoretic mobility shift assay revealed several binding sites for GATA4 and Nkx2.5 within the Id2 promoter. By further deletion and mutation analysis of the respective binding site, we identified that two motifs located at -497/-502 and -264/-270 were functionally important for Id2 promoter activation by GATA4 and Nkx2.5, respectively. Overexpression of GATA4 and/or Nkx2.5 induced not only Id2 promoter activity but also Id2 protein expression. Additionally, Id proteins significantly inhibit the GATA4 and Nkx2.5-dependent transcription, suggesting Id proteins may play a regulatory role in cardiogenesis. Collectively, our results demonstrate that GATA4 and Nkx2.5 could be one of the upstream regulators of Id2.
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