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首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Genomic organization, chromosomal localization and adipocytic expression of the murine gene for CORS-26 (collagenous repeat-containing sequence of 26 kDa protein)
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Genomic organization, chromosomal localization and adipocytic expression of the murine gene for CORS-26 (collagenous repeat-containing sequence of 26 kDa protein)

机译:CORS-26(含胶原重复序列的26 kDa蛋白序列)的鼠基因的基因组组织,染色体定位和脂肪表达

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摘要

The murine gene for CORS-26 shows striking homologies to the adipocyte-specific secretory protein adiponectin (belonging to the newly discovered Clq/TNF molecular superfamily) and its expression has been reported to be restricted to fibroblasts, cartilage and kidney. However, the present data demonstrate specific induction of CORS-26 mRNA expression in hormonally differentiated 3T3-L1 adipocytes, but not in preadipocytes. Furthermore, CORS-26 mRNA expression could be demonstrated in human synovial adipocytes of the knee by in situ hybridization. Since the genes for CORS-26 and adiponectin are homologous for their COOH-terminal globular domain and of their N-terminal collagenous domain, they might have originated by divergence from an innate mesenchymal precursor molecule directing the development of myocytes, adipocytes and chondrocytes from a mesenchymal stem cell. Here, the complete genomic organization with exon/intron boundaries together with exon-specific primer combinations are presented. Additionally, ~1 kb of the TATA-box-containing promoter region was cloned and analyzed for putative transcription factor binding sites. The chromosomal localization of the murine CORS-26 gene was mapped to mouse chromosome 15 A2 by fluorescence in situ hybridization (FISH). Since the linkage loci for proteolgycan-induced arthritis and MRL/lpr arthritis in mice have been mapped to that chromosomal region. CORS-26 might present the underlying mechanism of disease. The present data provide the basis for further investigation of the CORS-26 gene regulation in the context of mesenchymal tissue development, chondrocyte/adipocyte function and bone or skeletal disease.
机译:CORS-26的鼠基因与脂肪细胞特异性分泌蛋白脂联素(属于新发现的Clq / TNF分子超家族)表现出惊人的同源性,据报道其表达仅限于成纤维细胞,软骨和肾脏。但是,本数据表明在激素分化的3T3-L1脂肪细胞中特异性诱导CORS-26 mRNA表达,而在前脂肪细胞中则没有。此外,可以通过原位杂交在膝盖的人滑膜脂肪细胞中证明CORS-26 mRNA的表达。由于CORS-26和脂联素的基因在其COOH末端球状结构域和其N末端胶原结构域中是同源的,因此它们可能是由先天的间充质前体分子的发散起源的,该分子指导心肌细胞,脂肪细胞和软骨细胞的发育。间充质干细胞。在此,介绍了具有外显子/内含子边界以及外显子特异性引物组合的完整基因组组织。此外,克隆了约1 kb的含有TATA-box的启动子区域,并分析了假定的转录因子结合位点。通过荧光原位杂交(FISH)将鼠CORS-26基因的染色体定位映射到小鼠15 A2染色体。由于小鼠中蛋白聚糖引起的关节炎和MRL / lpr关节炎的连锁基因已被定位到该染色体区域。 CORS-26可能是疾病的潜在机制。本数据为在间充质组织发育,软骨细胞/脂肪细胞功能以及骨骼或骨骼疾病的背景下进一步研究CORS-26基因调控提供了基础。

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