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Site-specific DNA binding of nuclear factor I: analyses of cellular binding sites.

机译:核因子I的位点特异性DNA结合:细胞结合位点的分析。

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摘要

Nuclear factor I is a cellular site-specific DNA-binding protein required for the efficient in vitro replication of adenovirus DNA. We have characterized human DNA sequences to which nuclear factor I binds. Three nuclear factor I binding sites (FIB sites), isolated from HeLa cell DNA, each contain the sequence TGG(N)6-7GCCAA. Comparison with other known and putative FIB sites suggests that this sequence is important for the binding of nuclear factor I. Nuclear factor I protects a 25- to 30-base-pair region surrounding this sequence from digestion by DNase I. Methylation protection studies suggest that nuclear factor I interacts with guanine residues within the TGG(N)6-7GCCAA consensus sequence. One binding site (FIB-2) contained a restriction endonuclease HaeIII cleavage site (GGCC) at the 5' end of the GCCAA motif. Digestion of FIB-2 with HaeIII abolished the binding of nuclear factor I. Southern blot analyses indicate that the cellular FIB sites described here are present within single-copy DNA in the HeLa cell genome.
机译:核因子I是腺病毒DNA高效体外复制所需的细胞位点特异性DNA结合蛋白。我们已经表征了与核因子I结合的人类DNA序列。从HeLa细胞DNA分离出的三个核因子I结合位点(FIB位点),每个都包含序列TGG(N)6-7GCCAA。与其他已知和公认的FIB位点的比较表明,该序列对于结合核因子I很重要。核因子I保护该序列周围的25至30个碱基对的区域,避免被DNase I消化。甲基化保护研究表明核因子I与TGG(N)6-7GCCAA共有序列内的鸟嘌呤残基相互作用。一个结合位点(FIB-2)在GCCAA基序的5'端含有一个限制性核酸内切酶HaeIII切割位点(GGCC)。用HaeIII消化FIB-2消除了核因子I的结合。Southern印迹分析表明,此处描述的细胞FIB位点存在于HeLa细胞基因组的单拷贝DNA中。

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