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癌症中的转运RNA改变

tRNA alterations in cancer.

作者信息

Randerath K, Agrawal H P, Randerath E

出版信息

Recent Results Cancer Res. 1983;84:103-20. doi: 10.1007/978-3-642-81947-6_7.

Abstract
  1. 3H-, 125I-, and 32P-labeling methods were developed for base composition and sequence analysis of minute amounts of nonradioactive nucleic acids containing modified constituents. 2. Base composition analysis showed tRNA from two "liver-like" minimal deviation hepatomas, Morris hepatomas 5123D and 7777, to exhibit typical alterations when compared with liver tRNA. Our observations, which were made for different transplant generations of the tumors, indicated a trend toward undermethylation and undermodification of tRNA. 3. Sequence analysis of several cytoplasmic and mitochondrial tRNAs from hepatoma 5123D showed partial lack of m2G and complete lack of Gm and Q. 4. Sequence analysis of mitochondrial tRNAs from hepatoma 5123D indicated several instances of alterations of primary structure, a phenomenon not previously observed for cytoplasmic tRNAs from neoplasms. 5. Biochemical mechanisms underlying these alterations, as well as their functional implications, have yet to be investigated. 6. Modification patterns, but not primary structures, of mitochondrial tRNAs have been highly conserved when compared to prokaryotic and eukaryotic cytoplasmic tRNAs. This implies that (a) post-transcriptional modifications must play a crucial role in tRNA function, and (b) alterations of post-transcriptional modifications in tumor tRNAs have to be regarded as highly significant deviations from the norm.
摘要
  1. 开发了3H、125I和32P标记方法,用于对含有修饰成分的微量非放射性核酸进行碱基组成和序列分析。2. 碱基组成分析表明,与肝脏tRNA相比,来自两种“类肝脏”微小偏差肝癌(莫里斯肝癌5123D和7777)的tRNA表现出典型变化。我们对肿瘤不同移植代次的观察表明,tRNA存在甲基化不足和修饰不足的趋势。3. 对肝癌5123D的几种细胞质和线粒体tRNA进行序列分析,结果显示部分缺乏m2G,完全缺乏Gm和Q。4. 对肝癌5123D的线粒体tRNA进行序列分析,发现了几例一级结构改变的情况,这是之前在肿瘤细胞质tRNA中未观察到的现象。5. 这些改变背后的生化机制及其功能意义尚待研究。6. 与原核生物和真核生物细胞质tRNA相比,线粒体tRNA的修饰模式而非一级结构具有高度保守性。这意味着:(a)转录后修饰必定在tRNA功能中起关键作用;(b)肿瘤tRNA中转录后修饰的改变必须被视为严重偏离正常状态。

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