Ro-Choi Tae Suk, Choi Yong Chun
Departments of Pharmacology and Biochemistry, College of Medicine, Dong-A University, 3-1 Dong Dae Shin Dong, Seo Gu, Busan 602-714, Republic of Korea.
J Nucleic Acids. 2012;2012:369058. doi: 10.1155/2012/369058. Epub 2012 Jan 12.
In the study of cellular RNA chemistry, a major thrust of research focused upon sequence determinations for decades. Structures of snRNAs (4.5S RNA I (Alu), U1, U2, U3, U4, U5, and U6) were determined at Baylor College of Medicine, Houston, Tex, in an earlier time of pregenomic era. They show novel modifications including base methylation, sugar methylation, 5'-cap structures (types 0-III) and sequence heterogeneity. This work offered an exciting problem of posttranscriptional modification and underwent numerous significant advances through technological revolutions during pregenomic, genomic, and postgenomic eras. Presently, snRNA research is making progresses involved in enzymology of snRNA modifications, molecular evolution, mechanism of spliceosome assembly, chemical mechanism of intron removal, high-order structure of snRNA in spliceosome, and pathology of splicing. These works are destined to reach final pathway of work "Function and Structure of Spliceosome" in addition to exciting new exploitation of other noncoding RNAs in all aspects of regulatory functions.
在细胞RNA化学研究中,几十年来研究的一个主要方向集中在序列测定上。在德克萨斯州休斯顿的贝勒医学院,在前基因组时代的早期就确定了小核RNA(4.5S RNA I(Alu)、U1、U2、U3、U4、U5和U6)的结构。它们显示出包括碱基甲基化、糖甲基化、5'-帽结构(0-III型)和序列异质性在内的新型修饰。这项工作提出了一个关于转录后修饰的有趣问题,并在前基因组、基因组和后基因组时代通过技术革命取得了许多重大进展。目前,小核RNA研究正在酶学修饰、分子进化、剪接体组装机制、内含子去除的化学机制、剪接体中小核RNA的高阶结构以及剪接病理学等方面取得进展。除了在调控功能的各个方面对其他非编码RNA进行令人兴奋的新探索外,这些工作注定要通向“剪接体的功能与结构”这一最终研究路径。