Reardon B J, Gordon D, Ballard M J, Winter E
Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Nucleic Acids Res. 1995 Dec 11;23(23):4900-6. doi: 10.1093/nar/23.23.4900.
The DAT1 gene of Saccharomyces cerevisiae encodes a DNA binding protein (Dat1p) that specifically recognizes the minor groove of non-alternating oligo(A).oligo(T) tracts. Sequence-specific recognition requires arginine residues found within three perfectly repeated pentads (G-R-K-P-G) of the Dat1p DNA binding domain [Reardon, B. J., Winters, R. S., Gordon, D., and Winter, E. (1993) Proc. Natl. Acad. Sci. USA 90, 11327-1131]. This report describes a rapid and simple method for purifying the Dat1p DNA binding domain and the biochemical characterization of its interaction with oligo(A).oligo(T) tracts. Oligonucleotide binding experiments and the characterization of yeast genomic Dat1p binding sites show that Dat1p specifically binds to any 11 base sequence in which 10 bases conform to an oligo(A).oligo(T) tract. Binding studies of different sized Dat1p derivatives show that the Dat1p DNA binding domain can function as a monomer. Competition DNA binding assays using poly(I).poly(C), demonstrate that the minor groove oligo(A).oligo(T) constituents are not sufficient for high specificity DNA binding. These data constrain the possible models for Dat1p/oligo(A).oligo(T) complexes, suggest that the DNA binding domain is in an extended structure when complexed to its cognate DNA, and show that Dat1p binding sites are more prevalent than previously thought.
酿酒酵母的DAT1基因编码一种DNA结合蛋白(Dat1p),该蛋白能特异性识别非交替寡聚(A)·寡聚(T)序列的小沟。序列特异性识别需要在Dat1p DNA结合结构域的三个完美重复的五肽(G-R-K-P-G)中发现的精氨酸残基[里尔登,B. J.,温特斯,R. S.,戈登,D.,以及温特,E.(1993年)《美国国家科学院院刊》90,11327 - 1131]。本报告描述了一种快速简便的纯化Dat1p DNA结合结构域的方法及其与寡聚(A)·寡聚(T)序列相互作用的生化特性。寡核苷酸结合实验以及酵母基因组Dat1p结合位点的特性表明,Dat1p特异性结合任何11个碱基的序列,其中10个碱基符合寡聚(A)·寡聚(T)序列。不同大小的Dat1p衍生物的结合研究表明,Dat1p DNA结合结构域可以作为单体发挥作用。使用聚(I)·聚(C)进行的竞争DNA结合测定表明,小沟寡聚(A)·寡聚(T)成分不足以实现高特异性DNA结合。这些数据限制了Dat1p/寡聚(A)·寡聚(T)复合物的可能模型,表明DNA结合结构域在与其同源DNA结合时处于伸展结构,并表明Dat1p结合位点比以前认为的更普遍。