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莫里斯肝癌5123D 丝氨酸tRNA1IGA中鸟苷17处缺乏特定的核糖甲基化。

Lack of a specific ribose methylation at guanosine 17 in Morris hepatoma 5123D tRNASer1IGA.

作者信息

Randerath E, Gopalakrishnan A S, Gupta R C, Agrawal H P, Randerath K

出版信息

Cancer Res. 1981 Jul;41(7):2863-7.

PMID:7248946
Abstract

Tumor transfer RNA's (tRNA's) frequently exhibit alterations in column chromatographic profiles and in base compositions when compared to their normal counterparts. Because such alterations may be involved in the dedifferentiated state of cancer cells, it is of interest to determine their structural basis and functional significance. The recent development of highly sensitive postlabeling methods has now made possible sequence analysis of tRNA's from neoplastic tissues available only in limited amounts. We have determined the nucleotide sequence of Morris hepatoma serine tRNA (anticodon IGA) and compared it with its normal counterpart in rat liver. The tumor serine tRNA was found to lack the ribose methylation of guanosine in position 17 of the dihydrouridine loop present in the liver RNA. This result explains the column chromatographic shifts of Morris hepatoma 5123D seryl-tRNA isoacceptors, suggesting that all seryl-tRNA isoacceptors may lack this modification.

摘要

与正常对应物相比,肿瘤转移核糖核酸(tRNA)在柱色谱图谱和碱基组成方面常常表现出改变。由于此类改变可能与癌细胞的去分化状态有关,因此确定其结构基础和功能意义很有意义。高灵敏度后标记方法的最新发展,现已使得对仅少量可得的肿瘤组织tRNA进行序列分析成为可能。我们已确定了莫里斯肝癌丝氨酸tRNA(反密码子IGA)的核苷酸序列,并将其与其在大鼠肝脏中的正常对应物进行了比较。发现肿瘤丝氨酸tRNA在肝脏RNA二氢尿嘧啶环的第17位鸟苷处缺乏核糖甲基化。这一结果解释了莫里斯肝癌5123D丝氨酰 - tRNA同工受体的柱色谱迁移,表明所有丝氨酰 - tRNA同工受体可能都缺乏这种修饰。

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