Sakamoto N, Chastain P D, Parniewski P, Ohshima K, Pandolfo M, Griffith J D, Wells R D
Institute of Biosciences and Technology, Texas A & M University, Texas Medical Center, Houston 77030-3303, USA.
Mol Cell. 1999 Apr;3(4):465-75. doi: 10.1016/s1097-2765(00)80474-8.
A novel DNA structure, sticky DNA, is described for lengths of (GAA.TTC)n found in intron 1 of the frataxin gene of Friedreich's ataxia patients. Sticky DNA is formed by the association of two purine.purine.pyrimidine (R.R.Y) triplexes in negatively supercoiled plasmids at neutral pH. An excellent correlation was found between the lengths of (GAA.TTC) (> 59 repeats): first, in FRDA patients, second, required to inhibit transcription in vivo and in vitro, and third, required to adopt the sticky conformation. Fourth, (GAAGGA.TCCTTC)65, also found in intron 1, does not form sticky DNA, inhibit transcription, or associate with the disease. Hence, R.R.Y triplexes and/or sticky DNA may be involved in the etiology of FRDA.
一种新的DNA结构——粘性DNA,在弗里德赖希共济失调患者的frataxin基因内含子1中发现的(GAA.TTC)n片段中被描述。粘性DNA是由两个嘌呤-嘌呤-嘧啶(R.R.Y)三链体在中性pH下的负超螺旋质粒中缔合形成的。在(GAA.TTC)的长度(>59个重复序列)之间发现了极好的相关性:第一,在FRDA患者中;第二,体内和体外抑制转录所需的长度;第三,形成粘性构象所需的长度。第四,在内含子1中也发现的(GAAGGA.TCCTTC)65不形成粘性DNA,不抑制转录,也与该疾病无关。因此,R.R.Y三链体和/或粘性DNA可能参与了FRDA的病因。