STRUCTURE AND FUNCTION OF NUCLEIC ACIDS

核酸的结构和功能

• 批准号: 3281678
• 负责人: JOHN N ABELSON
• 金额: $ 32.77万
• 依托单位: CALIFORNIA INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 1983
• 资助国家: 美国
• 起止时间: 1983-03-01 至 1986-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3281678
• 关键词: Escherichia coli; Saccharomyces; bacterial RNA; bacterial genetics; bacteriophage T4; gene expression; genetic manipulation; genetic regulation; genetic transcription; messenger RNA; microorganism genetics; mutant; nucleic acid chemical synthesis; nucleic acid sequence; transfer RNA; virus RNA; virus genetics; virus infection mechanism; wheat

This project is concerned with the control of gene expression and two aspects of this problem are currently being investigataed. Control fo gene expression may be exerted at the levels of initiation of transcription. We have studied the mechanisms of transcriptional control in two bacterial operons, the lac operon and the boitin operon. Currently we are studying the control of the programmed pattern of transcriptional initiation during the infectious cycle of bacteriophage T4. We are also concerned with the control of expression and the function of the actin gene in S. cerevisiae. Most RNA molecules are post-transcriptionally altered in a series of reactions collectively known as RNA processing. It is now clear that RNA processing plays a major role in the expression of eukaryotic genes. The recent elucidation of eukaryotic gene structures has revealed a new principle of organization. Eukaryotic genes are frequently interrupted by non-coding sequences known as intervening sequences or introns. These sequences are removed from RNA precursors in a new processing reaction called RNA splicing. We were the first to demonstrate the RNA splicing reaction in vitro - in this ase with yeast tRNA precursors. We are continuing the study of the tRNA splicing reaction and propose procedures for the investigation of mRNA splicing. Powerful new techniques have recently been developed allowing the in vitro alteration of genes and their return to the organism (transformation). The most powerful of the mutagenic strategies requires the organic synthesis of oligonucleotides by techniques which derive from the pioneering efforts of Khorana. We propose to use these techniques to synthesize oligonucleotides to produce precise alterations of genes in order to study the mechanism of control of RNA synthesis.

该项目涉及基因表达的控制和两个 这个问题的某些方面目前正在得到解决。 控制fo基因 表达可以在转录起始的水平发挥作用。 我们 研究了两种细菌的转录控制机制， lac操纵子和boitin操纵子。 目前，我们正在研究 转录起始的程序化模式的控制， 噬菌体T4的感染周期 我们还关注 肌动蛋白基因在S.啤酒。 大多数RNA分子在一系列转录后改变， 这些反应统称为RNA加工。 现在很清楚，RNA 加工在真核基因的表达中发挥着重要作用。 的 最近对真核基因结构的阐明揭示了一种新的 组织原则。 真核基因经常被 称为插入序列或内含子的非编码序列。 这些 在新的加工反应中， 称为RNA剪接。 我们是第一个在体外证明RNA剪接反应的人， 这种酶与酵母tRNA前体。 我们正继续研究 tRNA剪接反应和mRNA研究的建议程序 拼接 最近已经开发出了强大的新技术， 基因的改变和它们返回到生物体（转化）。 的 最强大的诱变策略需要有机合成 寡核苷酸的技术，来自开拓性的努力， Khorana. 我们建议使用这些技术来合成寡核苷酸 来精确地改变基因， 控制RNA合成。