Arid5a cooperates with Sox9 to stimulate chondrocyte-specific transcription

Author:

Amano Katsuhiko12,Hata Kenji1,Muramatsu Shuji3,Wakabayashi Makoto13,Takigawa Yoko1,Ono Koichiro1,Nakanishi Masako1,Takashima Rikako1,Kogo Mikihiko2,Matsuda Akio3,Nishimura Riko1,Yoneda Toshiyuki1

Affiliation:

1. Department of Molecular and Cellular Biochemistry, Osaka University Graduate School of Dentistry, Osaka 565–0871, Japan

2. Department of Oral and Maxillofacial Surgery, Osaka University Graduate School of Dentistry, Osaka 565–0871, Japan

3. Asahikasei Pharma, Shizuoka 410–2321, Japan

Abstract

SRY-box–containing gene 9 (Sox9) is an essential transcription factor in chondrocyte lineage determination and differentiation. Recent studies demonstrated that Sox9 controls the transcription of chondrocyte-specific genes in association with several other transcriptional regulators. To further understand the molecular mechanisms by which Sox9 influences transcriptional events during chondrocyte differentiation, we attempted to identify transcriptional partners of Sox9 and to examine their roles in chondrocyte differentiation. We isolated AT-rich interactive domain–containing protein 5a (Arid5a; also known as Mrf1) as an activator of the Col2a1 gene promoter from an ATDC5 cDNA library. Arid5a was highly expressed in cartilage and induced during chondrocyte differentiation. Furthermore, Arid5a physically interacted with Sox9 in nuclei and up-regulated the chondrocyte-specific action of Sox9. Overexpression of Arid5a stimulated chondrocyte differentiation in vitro and in an organ culture system. In contrast, Arid5a knockdown inhibited Col2a1 expression in chondrocytes. In addition, Arid5a binds directly to the promoter region of the Col2a1 gene and stimulates acetylation of histone 3 in the region. Our results suggest that Arid5a may directly interact with Sox9 and thereby enhance its chondrocyte-specific action.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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