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Cloning and expression of two human genes encoding calcium-binding proteins that are regulated during myeloid differentiation.

机译:编码钙结合蛋白的两个人类基因的克隆和表达它们在髓样分化过程中受到调节。

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摘要

The cellular mechanisms involved in chronic inflammatory processes are poorly understood. This is especially true for the role of macrophages, which figure prominently in the inflammatory response. Two proteins, MRP8 and MRP14, which are expressed in infiltrate macrophages during inflammatory reactions but not in normal tissue macrophages, have been characterized. Here we report that MRP8 and MRP14 mRNAs are specifically expressed in human cells of myeloid origin and that their expression is regulated during monocyte-macrophage and granulocyte differentiation. To initiate the analysis of cis-acting elements governing the tissue-specific expression of the MRP genes, we cloned the human genes encoding MRP8 and MRP14. Both genes contain three exons, are single copy, and have a strikingly similar organization. They belong to a novel subfamily of highly homologous calcium-binding proteins which includes S100 alpha, S100 beta, intestinal calcium-binding protein, P11, and calcyclin (2A9). A transient expression assay was devised to investigate the tissue-specific regulatory elements responsible for MRP gene expression after differentiation in leukemia HL60 cells. The results of this investigation demonstrated that the cis-acting elements responsible for MRP expression are present on the cloned DNA fragment containing the MRP gene loci.
机译:慢性炎症过程涉及的细胞机制了解甚少。对于巨噬细胞的作用尤其如此,其在炎症反应中占重要地位。已经表征了两种蛋白,MRP8和MRP14,它们在炎症反应过程中在浸润性巨噬细胞中表达,但在正常组织巨噬细胞中不表达。在这里我们报告说,MRP8和MRP14 mRNA在髓样来源的人类细胞中特异性表达,并且它们的表达在单核巨噬细胞和粒细胞分化过程中受到调节。为了开始分析控制MRP基因的组织特异性表达的顺式作用元件,我们克隆了编码MRP8和MRP14的人类基因。这两个基因均包含三个外显子,均为单拷贝,并具有惊人相似的组织。它们属于高度同源的钙结合蛋白的新亚家族,包括S100 alpha,S100 beta,肠钙结合蛋白,P11和钙环蛋白(2A9)。设计了一种瞬时表达测定法,以研究白血病HL60细胞分化后负责MRP基因表达的组织特异性调控元件。这项研究的结果表明,负责MRP表达的顺式作用元件存在于含有MRP基因位点的克隆DNA片段上。

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