Du Quan, Smith Chaim, Shiffeldrim Nahum, Vologodskaia Maria, Vologodskii Alexander
Department of Chemistry, New York University, New York, NY 10003, USA.
Proc Natl Acad Sci U S A. 2005 Apr 12;102(15):5397-402. doi: 10.1073/pnas.0500983102. Epub 2005 Apr 4.
Cloutier and Widom [Cloutier, T. E. & Widom, J. (2004) Mol. Cell 14, 355-362] recently reported that the cyclization efficiency of short DNA fragments, about 100 bp in length, exceeds theoretical expectations by three orders of magnitude. In an effort to resolve this discrepancy, we tried modifying the theory. We investigated how the distribution of the angles between adjacent base pairs of the double helix affects the cyclization efficiency. We found that only the incorporation of sharp kinks in the angle distribution provides the desired increase of the cyclization efficiency. We did not find a model, however, that fits all cyclization data for DNA fragments of different lengths. Therefore, we carefully reinvestigated the cyclization of 100-bp DNA fragments experimentally and found their cyclization efficiency to be in remarkable agreement with the traditional model of DNA bending. We also found an explanation for the discrepancy between our results and those of Cloutier and Widom.
克劳捷和威登[克劳捷,T. E. & 威登,J.(2004年)《分子细胞》第14卷,第355 - 362页]最近报道,长度约100碱基对的短DNA片段的环化效率比理论预期高出三个数量级。为了解决这一差异,我们尝试修改理论。我们研究了双螺旋相邻碱基对之间角度的分布如何影响环化效率。我们发现,只有在角度分布中引入急剧的弯折才能使环化效率达到预期的提高。然而,我们没有找到一个能拟合不同长度DNA片段所有环化数据的模型。因此,我们通过实验仔细重新研究了100碱基对DNA片段的环化,发现它们的环化效率与传统的DNA弯曲模型非常吻合。我们还找到了我们的结果与克劳捷和威登的结果之间存在差异的解释。