Department of Chemistry, University of Nebraska, Lincoln, Nebraska 68588, USA.
J Phys Chem B. 2010 Mar 11;114(9):3285-93. doi: 10.1021/jp9091656.
DNA damage has been implicated in numerous human diseases, particularly cancer, and the aging process. Single-base lesions, such as uracil, in DNA can be cytotoxic or mutagenic and are recognized by a DNA glycosylase during the process of base excision repair. Increased dynamic properties in lesion-containing DNAs have been suggested to assist recognition and specificity. Deuterium solid-state nuclear magnetic resonance (SSNMR) has been used to directly observe local dynamics of the furanose ring within a uracil:adenine (U:A) base pair and compared to a normal thymine:adenine (T:A) base pair. Quadrupole echo lineshapes, <T(1Z)>, and <T(2e)> relaxation data were collected, and computer modeling was performed. The results indicate that the relaxation times are identical within the experimental error, the solid lineshapes are essentially indistinguishable above the noise level, and our lineshapes are best fit with a model that does not have significant local motions. Therefore, U:A base pair furanose rings appear to have essentially identical dynamic properties as a normal T:A base pair, and the local dynamics of the furanose ring are unlikely to be the sole arbiter for uracil recognition and specificity in U:A base pairs.
DNA 损伤与许多人类疾病有关,尤其是癌症和衰老过程。DNA 中的单碱基损伤,如尿嘧啶,可以是细胞毒性的或诱变的,并在碱基切除修复过程中被 DNA 糖苷酶识别。含损伤 DNA 的动态特性增加被认为有助于识别和特异性。氘固态核磁共振(SSNMR)已被用于直接观察尿嘧啶:腺嘌呤(U:A)碱基对中呋喃糖环的局部动力学,并与正常胸腺嘧啶:腺嘌呤(T:A)碱基对进行比较。收集了四极回波线形状,<T(1Z)>和<T(2e)>弛豫数据,并进行了计算机建模。结果表明,在实验误差范围内弛豫时间相同,在噪声水平以上实线形状基本无法区分,并且我们的线形状与没有明显局部运动的模型拟合最好。因此,U:A 碱基对的呋喃糖环的动态特性与正常的 T:A 碱基对基本相同,并且呋喃糖环的局部动力学不太可能是 U:A 碱基对中尿嘧啶识别和特异性的唯一仲裁者。