Hida Mariko, Hamanaka Ryoji, Okamoto Osamu, Yamashita Kouhei, Sasaki Takako, Yoshioka Hidekatsu, Matsuo Noritaka
Department of Matrix Medicine, Faculty of Medicine, Oita University, 1-1 Idaigaoka, Hasama-machi, Yufu, Oita, 879-5593, Japan.
In Vitro Cell Dev Biol Anim. 2014 Apr;50(4):358-66. doi: 10.1007/s11626-013-9692-3. Epub 2013 Oct 3.
Type XI collagen, a heterotrimer composed of α1(XI), α2(XI), and α3(XI), plays a critical role in cartilage formation and in skeletal morphogenesis. However, the transcriptional regulation of α1(XI) collagen gene (Col11a1) in chondrocyte is poorly characterized. In this study, we investigated the proximal promoter of mouse Col11a1 gene in chondrocytes. Major transcription start site was located at -299 bp upstream of the translation start site, and the proximal promoter lacks a TATA sequence but has a high guanine-cytosine (GC) content. Cell transfection experiments demonstrated that the segment from -116 to -256 is necessary for activation of the proximal Col11a1 promoter, and an electrophoretic mobility shift assay showed that a nuclear protein is bound to the segment from -116 to -176 in this promoter. Additional comparative and in silico analyses demonstrated that an ATTGG sequence, which is critical for binding to nuclear factor Y (NF-Y), is within the highly conserved region from -135 to -145. Interference assays using wild-type and mutant oligonucleotide or with specific antibody revealed that NF-Y protein is bound to this region. Cell transfection experiments with reporter constructs in the absence of NF-Y binding sequence exhibited the suppression of the promoter activity. Furthermore, chromatin immunoprecipitation assay demonstrated that NF-Y protein is directly bound to this region in vivo, and overexpression of dominant-negative NF-Y A mutant also inhibited the proximal promoter activity. Taken together, these results indicate that the transcription factor NF-Y regulates the proximal promoter activity of mouse Col11a1 gene in chondrocytes.
XI型胶原蛋白是一种由α1(XI)、α2(XI)和α3(XI)组成的异源三聚体,在软骨形成和骨骼形态发生中起关键作用。然而,软骨细胞中α1(XI)胶原蛋白基因(Col11a1)的转录调控特征尚不明确。在本研究中,我们研究了小鼠Col11a1基因在软骨细胞中的近端启动子。主要转录起始位点位于翻译起始位点上游-299 bp处,近端启动子缺乏TATA序列,但鸟嘌呤-胞嘧啶(GC)含量较高。细胞转染实验表明,-116至-256片段对于激活近端Col11a1启动子是必需的,电泳迁移率变动分析表明,一种核蛋白与该启动子中-116至-176片段结合。进一步的比较分析和计算机分析表明,对结合核因子Y(NF-Y)至关重要的ATTGG序列位于-135至-145的高度保守区域内。使用野生型和突变型寡核苷酸或特异性抗体的干扰试验表明,NF-Y蛋白与该区域结合。在没有NF-Y结合序列的情况下用报告基因构建体进行的细胞转染实验显示启动子活性受到抑制。此外,染色质免疫沉淀试验表明,NF-Y蛋白在体内直接与该区域结合,显性负性NF-Y A突变体的过表达也抑制了近端启动子活性。综上所述,这些结果表明转录因子NF-Y调节小鼠Col11a1基因在软骨细胞中的近端启动子活性。