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序列导向的弯曲DNA螺旋是克氏锥虫切口酶的特异性结合位点。

Sequence-directed bent DNA helix is the specific binding site for Crithidia fasciculata nicking enzyme.

作者信息

Linial M, Shlomai J

机构信息

Kuvin Centre for the Study of Infectious and Tropical Diseases, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Proc Natl Acad Sci U S A. 1987 Dec;84(23):8205-9. doi: 10.1073/pnas.84.23.8205.

Abstract

The sequence-directed bent structure of kinetoplast DNA minicircles specifies a unique binding site for Crithidia fasciculata nicking enzyme. Binding of the purified enzyme to the bent structure results in the formation of a tight enzyme-DNA complex that is highly specific to curved DNA. Recognition of the binding site is not determined by the nucleotide sequence at the site of binding per se but through the specific local variation in the DNA helix geometry. Both dynamic curved structures, which are generated by supercoiling, and static ones, which are sequenced-directed, could support and efficient enzyme-DNA complex formation. Binding interactions are dependent upon the degree of the helix curvature and decrease with the straightening of the binding site. DNase I protection experiments identify distinct domains of enzyme binding within the bent structure and suggest the induction of structural changes within these regions as a result of protein-DNA interactions.

摘要

动质体DNA小环的序列导向弯曲结构为克氏锥虫切口酶指定了一个独特的结合位点。纯化后的酶与弯曲结构的结合导致形成紧密的酶-DNA复合物,该复合物对弯曲DNA具有高度特异性。结合位点的识别并非由结合位点本身的核苷酸序列决定,而是通过DNA螺旋几何结构中的特定局部变化来确定。由超螺旋产生的动态弯曲结构和序列导向的静态弯曲结构都能支持并有效形成酶-DNA复合物。结合相互作用取决于螺旋曲率的程度,并随着结合位点的伸直而降低。DNA酶I保护实验确定了弯曲结构内酶结合的不同结构域,并表明由于蛋白质-DNA相互作用,这些区域内会诱导结构变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ab0/299510/4f950a2cca37/pnas00338-0042-a.jpg

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