Leegwater P A, van Driel W, van der Vliet P C
EMBO J. 1985 Jun;4(6):1515-21. doi: 10.1002/j.1460-2075.1985.tb03811.x.
Nuclear factor I is a 47-kd protein, isolated from nuclei of HeLa cells, that binds specifically to the inverted terminal repeat of the adenovirus (Ad) DNA and enhances Ad DNA replication in vitro. We have studied the DNA sequence specificity of nuclear factor I binding using cloned terminal fragments of the Ad2 genome and a set of deletion mutants. Binding of nuclear factor I protects nucleotides 19-42 of Ad2 DNA against DNase I digestion. Filter binding assays show that deletion of the first 23 nucleotides does not impair binding while a deletion of 24 nucleotides reduces binding severely. However, binding studies on Ad12 DNA indicate that nucleotide 24 can be mutated. Fragments containing the first 40 bp are bound normally while the first 38 bp are insufficient to sustain binding. Taken together, these results indicate that the minimal recognition site of nuclear factor I contains 15 or 16 nucleotides, located from nucleotide 25 to nucleotide 39 or 40 of the Ad2 DNA. This site contains two of the four conserved nucleotide sequences in this region. Sequences flanking the minimal recognition site may reduce the binding affinity of nuclear factor I. In accordance with these binding studies, DNA replication of a fragment that carries the sequence of the terminal 40 nucleotides of Ad2 at one molecular end is enhanced by nuclear factor I in an in vitro replication system.
核因子I是一种47千道尔顿的蛋白质,从HeLa细胞核中分离得到,它能特异性结合腺病毒(Ad)DNA的反向末端重复序列,并在体外增强Ad DNA复制。我们使用Ad2基因组的克隆末端片段和一组缺失突变体研究了核因子I结合的DNA序列特异性。核因子I的结合可保护Ad2 DNA的19 - 42位核苷酸不被DNase I消化。滤膜结合试验表明,缺失前23个核苷酸不会损害结合,而缺失24个核苷酸则会严重降低结合。然而,对Ad12 DNA的结合研究表明,第24位核苷酸可以发生突变。包含前40个碱基对的片段能正常结合,而前38个碱基对不足以维持结合。综上所述,这些结果表明核因子I的最小识别位点包含15或16个核苷酸,位于Ad2 DNA的第25位核苷酸至第39或40位核苷酸处。该位点包含该区域四个保守核苷酸序列中的两个。最小识别位点两侧的序列可能会降低核因子I的结合亲和力。根据这些结合研究,在体外复制系统中,核因子I可增强在一个分子末端携带Ad2末端40个核苷酸序列的片段的DNA复制。