Several regulators of E2F transcriptional activity, including the retinoblastoma tumor suppressor (Rb) protein, p16 Ink4a , cyclin D1, and cyclin-dependent kinase 4, have been shown to be targets for genetic alterations that underlie the development of human cancers. Deregulation of E2F transcriptio
Transcriptional regulation of fibrillin-2 gene by E2F family members in chondrocyte differentiation
✍ Scribed by Takuya Yanagino; Keizo Yuasa; Masami Nagahama; Yoshiko Matsuda; Akihiko Tsuji
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 391 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Mutation in fibrillin‐2, a major structural component of extracellular microfibrils in connective tissue, results in the autosomal dominant disease congenital contractural arachnodactyly. This genetic disease is characterized by dolichostenomelia and arachnodactyly, in addition to contractures of the large joints and abnormal pinnae formation, thus indicating the significance of fibrillin‐2 in chondrogenesis. In this study, we investigated the transcriptional regulation of fibrillin‐2 in chondrogenic differentiation. Although mRNA expression of fibrillin‐1, a highly homologous protein to fibrillin‐2, remained almost unchanged during chondrogenesis of mouse ATDC5 cells, fibrillin‐2 mRNA expression varied. Fibrillin‐2 was highly expressed at the early stage and declined progressively during differentiation. The 5′‐flanking region of the fibrillin‐2 gene contains potential binding sites for E2F, Runx, AP‐2, and Sox transcription factors. The promoter activity of fibrillin‐2 decreased markedly following deletion and mutagenesis of the E2F binding site between −143 and −136 bp. Overexpression of E2F1 resulted in a marked increase in its promoter activity, whereas expression of other transcription factors including AP‐2α and Runx2 had no effect. The increase in promoter activity by E2F1 was completely suppressed by the coexpression of E2F4. E2F2 and E2F3 had positive effects on the promoter activity. Although ATDC5 cells expressed transcripts for the E2F family genes at all stages of differentiation, the expression profiles differed. E2F1 expression remained almost unchanged, whereas E2F4 expression increased markedly at the late stage of differentiation. These results indicated that coordinated expression of the E2F family is critical for the transcriptional regulation of fibrillin‐2 during chondrogenesis. J. Cell. Biochem. 106: 580–588, 2009. © 2009 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract Epithelium specific Ets‐2 (ESE‐2), an epithelium‐specific ETS‐domain transcription factor, is highly expressed in differentiated keratinocytes. To understand the molecular mechanisms that govern the cell‐type and differentiation‐specific expression of ESE‐2 in keratinocytes, we have foc
## Abstract Various chemotherapeutic agents have been shown to sensitize cancer cells to members of the tumor necrosis factor (TNF) family. However, it is unclear whether sensitization by chemotherapeutic agents involves the transcriptional regulation of apoptosis‐related genes. In this study, we i
The mechanism by which transforming growth factor beta (TGFP) exerts growth stirnulatory effects was examined in C3HIlOT112 mouse fibroblasts by study of cell cycle regulation of the retinoblastoma gene product (pl 1 ORb) and transcriptional regulation of the p l 1 OKb-associated transcription facto