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CC趋化因子受体5(CCR5)的基因结构与启动子功能

Gene organization and promoter function for CC chemokine receptor 5 (CCR5).

作者信息

Guignard F, Combadiere C, Tiffany H L, Murphy P M

机构信息

Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.

出版信息

J Immunol. 1998 Jan 15;160(2):985-92.

PMID:9551938
Abstract

CC chemokine receptor 5 (CCR5) functions physiologically as a receptor for the leukocyte chemoattractants macrophage inflammatory protein-1alpha, macrophage inflammatory protein-1beta, and RANTES, and functions pathologically as a key cell entry coreceptor for HIV-1. The factors that regulate CCR5 expression may be useful therapeutic targets for HIV-1 infection. To identify nuclear regulatory factors, we have located and functionally characterized the CCR5 gene promoter. The gene consists of two exons separated by a 1.9-kb intron. Exon 1 contains 43 bp of the 5'-untranslated region; exon 2 contains 11 bp of the 5'-untranslated region and the complete open reading frame. Primer extension analysis identified two adjacent transcriptional start points (tsp) that map to the first 2 bp found in the longest known CCR5 cDNA sequence. A TATA box is present 31 bp upstream from the first tsp. CCR5 mRNA was detected constitutively in both primary human myeloid and lymphoid cells by Northern blot hybridization. Consistent with this, transcription of a chloramphenicol acetyltransferase reporter gene was constitutively activated in both transiently transfected myeloid and lymphoid cell lines by the 80-bp gene fragment located immediately upstream of the tsp. Deletion analysis located a strong silencer element between nucleotides -244 and -80, and a strong enhancer element between -486 and -244. These results suggest that the gene region between -486 and -1 may regulate the expression of CCR5 in monocyte/macrophages and T lymphocytes.

摘要

CC趋化因子受体5(CCR5)在生理功能上作为白细胞趋化因子巨噬细胞炎性蛋白-1α、巨噬细胞炎性蛋白-1β和调节激活正常T细胞表达和分泌的因子(RANTES)的受体,在病理功能上作为HIV-1关键的细胞进入共受体。调节CCR5表达的因子可能是治疗HIV-1感染的有用靶点。为了鉴定核调节因子,我们定位并对CCR5基因启动子进行了功能表征。该基因由两个外显子组成,中间隔着一个1.9kb的内含子。外显子1包含43bp的5'非翻译区;外显子2包含11bp的5'非翻译区和完整的开放阅读框。引物延伸分析确定了两个相邻的转录起始点(tsp),它们定位于已知最长CCR5 cDNA序列中发现的前2bp处。在第一个tsp上游31bp处存在一个TATA盒。通过Northern印迹杂交在原代人髓样细胞和淋巴细胞中均组成性地检测到CCR5 mRNA。与此一致的是,氯霉素乙酰转移酶报告基因的转录在瞬时转染的髓样和淋巴细胞系中均被tsp上游紧邻的80bp基因片段组成性激活。缺失分析确定了一个位于-244至-80核苷酸之间的强沉默元件,以及一个位于-486至-244之间的强增强子元件。这些结果表明,-486至-1之间的基因区域可能调节单核细胞/巨噬细胞和T淋巴细胞中CCR5的表达。

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