Gronostajski R M, Adhya S, Nagata K, Guggenheimer R A, Hurwitz J
Mol Cell Biol. 1985 May;5(5):964-71. doi: 10.1128/mcb.5.5.964-971.1985.
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.
核因子I是腺病毒DNA体外高效复制所需的一种细胞位点特异性DNA结合蛋白。我们已经对核因子I结合的人类DNA序列进行了特征分析。从HeLa细胞DNA中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。与其他已知和推测的FIB位点比较表明,该序列对核因子I的结合很重要。核因子I保护该序列周围25至30个碱基对的区域不被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,这里描述的细胞FIB位点存在于HeLa细胞基因组的单拷贝DNA中。