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与年龄相关的DNA修饰(I类化合物):生理和病理过程的调节作用

Age-related DNA modifications (I-compounds): modulation by physiological and pathological processes.

作者信息

Randerath K, Li D H, Randerath E

机构信息

Department of Pharmacology, Baylor College of Medicine, Houston, TX 77030.

出版信息

Mutat Res. 1990 May;238(3):245-53. doi: 10.1016/0165-1110(90)90016-5.

Abstract

I-compounds are covalent DNA modifications that can be detected and measured by 32P-postlabeling assay because of their DNA-adduct like properties. They accumulate in an age-dependent, highly reproducible manner in tissue DNA of untreated animals in the absence of exogenous carcinogens and, therefore, appear to arise via the interaction of DNA with endogenous reactants formed in the course of normal metabolism. Chromatographically, they exhibit a wide range of polarities, indicative of structural diversity. In addition to age-dependent increases, I-compound profiles exhibit prominent species-, sex-, tissue- and diet-dependent qualitative and quantitative differences. Natural-ingredient (chow) diets produce qualitative differences as well as substantially higher I-compound levels in rat liver and kidney, when compared with purified diets. Modified purified diets containing high carbohydrate, protein, or fat concentrations further modulate I-compound profiles. During liver regeneration, I-compounds behave like DNA adducts rather than m5 C in that their levels are not quickly restored. Treatment of rats with the hepatocarcinogens 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), CCl4, and peroxisome proliferators as well as with a choline-devoid hepatocarcinogenic diet depressed the age-related increases of I-compound levels in liver, the target organ. Additional 32P-labeled derivatives were observed only with the peroxisome proliferators and presumably represent DNA adducts of exogenous origin. No I-compounds were detected in a series of Morris hepatomas with different degrees of differentiation. Thus, loss of I-compounds may be associated with altered gene expression/dedifferentiation. On the other hand, the age-dependent accumulation of I-compounds and their adduct-like character suggest potential relations to aging-associated dysdifferentiation and initiation of cancer. Structural complexity indicates different biological roles of I-compounds.

摘要

I-化合物是共价DNA修饰,由于其类似DNA加合物的性质,可通过32P后标记分析法进行检测和测量。在没有外源性致癌物的情况下,它们以年龄依赖性、高度可重复的方式在未处理动物的组织DNA中积累,因此,似乎是通过DNA与正常代谢过程中形成的内源性反应物相互作用而产生的。在色谱分析中,它们表现出广泛的极性,表明结构具有多样性。除了年龄依赖性增加外,I-化合物谱还表现出显著的物种、性别、组织和饮食依赖性的定性和定量差异。与纯化饮食相比,天然成分(饲料)饮食在大鼠肝脏和肾脏中产生定性差异以及更高的I-化合物水平。含有高碳水化合物、蛋白质或脂肪浓度的改良纯化饮食进一步调节I-化合物谱。在肝脏再生过程中,I-化合物的行为类似于DNA加合物而不是5-甲基胞嘧啶,因为它们的水平不会迅速恢复。用肝癌致癌物2,3,7,8-四氯二苯并对二恶英(TCDD)、四氯化碳和过氧化物酶体增殖剂以及缺乏胆碱的致癌饮食处理大鼠,会抑制肝脏(靶器官)中I-化合物水平与年龄相关的增加。仅在过氧化物酶体增殖剂处理后观察到额外的32P标记衍生物,推测它们代表外源性DNA加合物。在一系列不同分化程度的莫里斯肝癌中未检测到I-化合物。因此,I-化合物的缺失可能与基因表达改变/去分化有关。另一方面,I-化合物的年龄依赖性积累及其加合物样特征表明它们与衰老相关的分化异常和癌症起始可能存在潜在关系。结构复杂性表明I-化合物具有不同的生物学作用。

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