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A Zinc Finger Transcription Factor, αA-Crystallin Binding Protein 1, Is a Negative Regulator of the Chondrocyte-Specific Enhancer of the α1(II) Collagen Gene

机译:锌指转录因子,αA-晶体蛋白结合蛋白1,是α1(II)胶原基因的软骨细胞特异性增强子的负调节剂

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Transcription of the type II collagen gene (Col2a1) is regulated by multiple cis-acting sites. The enhancer element, which is located in the first intron, is necessary for high-level and cartilage-specific expression of Col2a1. A mouse limb bud cDNA expression library was screened by theSaccharomyces cerevisiae one-hybrid screening method to identify protein factors bound to the enhancer. A zinc finger protein, αA-crystallin binding protein 1 (CRYBP1), which had been reported to bind to the mouse αA-crystallin gene promoter, was isolated. We herein demonstrate that CRYBP1 is involved in the negative regulation of Col2a1 enhancer activity. CRYBP1 mRNA expression was downregulated during chondrocyte differentiation in vitro. In situ hybridization analysis of developing mouse cartilage showed that CRYBP1 mRNA was also downregulated during mesenchymal condensation and that CRYBP1 mRNA was highly expressed by hypertrophic chondrocytes, but at very low levels by resting and proliferating chondrocytes. Expression of recombinant CRYBP1 in a transfected rat chondrosarcoma cell line inhibitedCol2a1 enhancer activity. Electrophoretic mobility shift assays showed that CRYBP1 bound a specific sequence within theCol2a1 enhancer and inhibited the binding of Sox9, an activator for Col2a1, to the enhancer. Cotransfection of CRYBP1 with Sox9 into BALB/c 3T3 cells inhibited activation of theCol2a1 enhancer by Sox9. These results suggest a novel mechanism that negatively regulates cartilage-specific expression ofCol2a1.
机译:II型胶原基因( Col2a1 )的转录受多个 cis 作用位点调控。位于第一个内含子的增强子元件对于 Col2a1 的高水平和软骨特异性表达是必需的。用酿酒酵母一杂交法筛选小鼠肢芽cDNA表达文库,鉴定与增强子结合的蛋白质因子。分离出锌指蛋白αA-晶状蛋白结合蛋白1(CRYBP1),据报道该蛋白与小鼠αA-crystallin基因启动子结合。我们在本文中证明CRYBP1参与了 Col2a1 增强子活性的负调控。体外软骨细胞分化过程中 CRYBP1 mRNA表达下调。发育中的小鼠软骨的原位杂交分析表明, CRYBP1 mRNA在间充质凝结过程中也被下调,并且 CRYBP1 mRNA在肥大软骨细胞中高表达,但在静息状态下的表达水平非常低。和增殖的软骨细胞。重组CRYBP1在转染大鼠软骨肉瘤细胞系中的表达抑制了 Col2a1 增强子的活性。电泳迁移率迁移分析表明,CRYBP1结合了 Col2a1 增强子中的特定序列,并抑制了 Col2a1 的激活剂Sox9与增强子的结合。将CRYBP1和Sox9共转染到BALB / c 3T3细胞中可抑制Sox9对 Col2a1 增强子的激活。这些结果表明负调节 Col2a1 软骨特异性表达的新机制。

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