Chandler S P, Fox K R
Department of Physiology & Pharmacology, University of Southampton, Bassett Crescent East, UK.
FEBS Lett. 1995 Feb 20;360(1):21-5. doi: 10.1016/0014-5793(95)00069-l.
We have used DNase I footprinting to examine the formation of intermolecular triple helices at a fragment containing the target sequence A11(AT)6.(AT)6T11, using oligonucleotides designed to form parallel T.AT and G.TA triplets. We find that, although (TG)6 does not form a complex with (AT)6.(AT)6, T11(TG)6 forms a stable structure producing a clear footprint which includes the (AT)6 portion of the target site. This complex is not formed in the presence of magnesium, but can be stabilised by either manganese or a triplex-binding ligand.
我们使用DNA酶I足迹法来检测在包含靶序列A11(AT)6.(AT)6T11的片段上分子间三链螺旋的形成情况,所使用的寡核苷酸旨在形成平行的T·AT和G·TA三联体。我们发现,虽然(TG)6不与(AT)6.(AT)6形成复合物,但T11(TG)6形成了一个稳定的结构,产生了一个清晰的足迹,其中包括靶位点的(AT)6部分。这种复合物在镁存在的情况下不会形成,但可以通过锰或三链结合配体来稳定。