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鉴定一种与主要组织相容性复合体I-Aβ基因S盒结合的转录因子。

Identification of a transcription factor that binds to the S box of the I-A beta gene of the major histocompatibility complex.

作者信息

Celada A, Gil P, McKercher S R, Maki R A

机构信息

Department de Fisiologia (Immunologia), Facultad de Biologia, Universtat de Barcelona, Spain.

出版信息

Biochem J. 1996 Feb 1;313 ( Pt 3)(Pt 3):737-44. doi: 10.1042/bj3130737.

Abstract

Class II genes of the MHC show a striking homology upstream of the transcription start site that is composed of three conserved sequences (S, X and Y boxes, each separated by 15-20 bp). The presence of the S-box sequence in the mouse MHC class II gene I-A Beta was examined for its influence on the expression of this gene. Deletion or mutation of the S box decreased the induction of chloramphenicol acetyltransferase (CAT) activity in B lymphocytes by 32%. In macrophages, deletion or mutation of the S box abolished interferon-gamma (IFN-gamma) inducibility of CAT activity. Using a gel-retardation assay, we have identified a nuclear factor whose binding site overlaps the 7-mer conserved sequence of the S box. This factor is present in lymphocytes, macrophages, mastocytes and fibroblasts. Surprisingly, binding of this nuclear factor to DNA was induced by IFN-gamma in bone-marrow-derived macrophages, but not in macrophage-like cell lines. The binding site for this factor was defined by DNase I footprinting and partially purified by using an affinity column containing double-stranded oligonucleotides containing a sequence of the S box. A prominent protein of 43 kDa was found that bound specifically to the S-box sequence.

摘要

MHC的II类基因在转录起始位点上游表现出显著的同源性,该区域由三个保守序列(S、X和Y框,每个框之间相隔15 - 20个碱基对)组成。研究了小鼠MHC II类基因I - Aβ中S框序列的存在对该基因表达的影响。S框的缺失或突变使B淋巴细胞中氯霉素乙酰转移酶(CAT)活性的诱导降低了32%。在巨噬细胞中,S框的缺失或突变消除了CAT活性的干扰素 - γ(IFN - γ)诱导性。通过凝胶阻滞试验,我们鉴定出一种核因子,其结合位点与S框的7聚体保守序列重叠。这种因子存在于淋巴细胞、巨噬细胞、肥大细胞和成纤维细胞中。令人惊讶的是,在骨髓来源的巨噬细胞中,IFN - γ可诱导这种核因子与DNA结合,但在巨噬细胞样细胞系中则不然。通过DNase I足迹法确定了该因子的结合位点,并使用含有包含S框序列的双链寡核苷酸的亲和柱进行了部分纯化。发现一种43 kDa的突出蛋白质能特异性结合S框序列。

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