GORDON CONFERENCE ON RNA EDITING
RNA 编辑戈登会议
基本信息
- 批准号:2849214
- 负责人:
- 金额:$ 2.09万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1999
- 资助国家:美国
- 起止时间:1999-03-20 至 1999-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
A Gordon Conference on RNA editing is planned for January 24-29, 1999
at the Doubletree hotel in Ventura, California. RNA editing is the
co- or post-transcriptional modification of RNA which results in the
insertion, deletion or substitution of nucleotides. RNA editing can
therefore correct, extend or diversify the information encoded within
the corresponding genomic sequence and can dramatically alter the
function of the modified RNAs. For example, editing events within
the mammalian central nervous system can increase the diversity of
neurotransmitter receptor expression and ser e to effectively
modulate neuronal signaling pathways. Equally significant is the
cellular regulation of many of the RNA editing processes which
provides for developmental, tissue-specific and metabolic fine tuning
of protein function and biochemical pathways. Our understanding of
molecular mechanisms underlying RNA editing and their biological
occurrence has reached a critical stage where cross-fertilization of
hypotheses and experimental approaches is essential for focus in the
next decade of research.
There are many common questions and experimental goals among
investigators of RNA editing despite the diversity of organisms
wherein editing occurs, and the apparent dissimilarities in sequences
which are modified. Important to the understanding of every editing
system is a basic description of the RNA substrates that are modified
by these processes. Similarly, questions of general interest
concerning the mechanism, specificity, fidelity and processivity of
RNA editing can be addressed with a combination of biochemical and
molecular biological techniques coupled with the development of in
vitro editing systems. In this regard the cis-active regulatory
elements and trans-acting factors mediating a number of editing
processes are being evaluated at both the molecular and enetic level.
Understanding the structure and function of these factors at the
level of common or divergent features among the different editing
systems is an important goal of the proposed Gordon Research
Conference. Still other editing systems have yet to advance to in
vitro systems or have been described only recently. The Gordon
Research Conference will foster information and technology transfer
which will promote developments in these areas.
The cellular and molecular aspects of RNA editing regulation are also
broadly being pursued at the level of evolution as well as the
occurance of editing activities in different tissues and during
development. The biological significance of RNA editing is a
recurring theme throughout all aspects of the proposed conference.
Finally, information about other forms of RNA processing is likely to
have implications for understanding RNA editing mechanisms, and vice
versa. Investigators working in other areas of RNA processing
therefore will participate in appropriate sessions to stimulate
exchange between these related fields.
关于RNA编辑的戈登会议计划于1999年1月24日至29日举行
在加州文图拉的双树酒店 RNA编辑是
RNA的共转录或转录后修饰,其导致
核苷酸的插入、缺失或取代。 RNA编辑可以
因此校正、扩展或多样化编码在
相应的基因组序列,并可以显着改变
修饰的RNA的功能。 例如,在
哺乳动物中枢神经系统可以增加
神经递质受体的表达,并有效地
调节神经信号通路。 同样重要的是,
许多RNA编辑过程的细胞调节,
提供发育、组织特异性和代谢微调
蛋白质功能和生物化学途径。 我们理解
RNA编辑的分子机制及其生物学意义
发生已经达到了一个关键阶段,
假设和实验方法是必不可少的重点,
未来十年的研究
有许多共同的问题和实验目标,
尽管生物体的多样性,
其中发生编辑,序列中明显的差异
其被修改。 对于理解每次编辑都很重要
系统是对被修饰的RNA底物的基本描述
通过这些过程。 同样,普遍感兴趣的问题
有关的机制,特异性,保真度和持续性,
RNA编辑可以通过生物化学和生物化学的组合来解决。
分子生物学技术的发展,
体外编辑系统。 在这方面,顺式活性调节
元素和trans-acting因素介导的一些编辑
目前正在分子和遗传水平上对这些进程进行评估。
了解这些因素的结构和功能,
不同编辑之间的共性或差异性水平
系统是戈登研究所的一个重要目标
会议 还有一些编辑系统尚未发展到
体外系统或最近才被描述。 戈登
研究会议将促进信息和技术转让
这将促进这些领域的发展。
RNA编辑调控的细胞和分子方面也是
在进化的层面上,
编辑活动在不同组织中的发生,
发展 RNA编辑的生物学意义是
在拟议的会议的所有方面反复出现的主题。
最后,关于其他形式的RNA加工的信息可能会
对理解RNA编辑机制有意义,
亦然 在RNA加工的其他领域工作的研究人员
因此,将参加适当的会议,以促进
这些相关领域的交流。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Ronald B. Emeson其他文献
Alternative production of calcitonin and CGRP mRNA is regulated at the calcitonin-specific splice acceptor
降钙素和 CGRP mRNA 的选择性产生在降钙素特异性剪接受体处受到调节
- DOI:
10.1038/341076a0 - 发表时间:
1989-09-07 - 期刊:
- 影响因子:48.500
- 作者:
Ronald B. Emeson;Farah Hedjran;Joanne M. Yeakley;Jeffrey W. Guise;Michael G. Rosenfeld - 通讯作者:
Michael G. Rosenfeld
Ronald B. Emeson的其他文献
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{{ truncateString('Ronald B. Emeson', 18)}}的其他基金
Cell-specific Modulation of Feeding Behavior by Serotonin 2C Receptor RNA Processing
5-羟色胺 2C 受体 RNA 加工对摄食行为的细胞特异性调节
- 批准号:
10216247 - 财政年份:2019
- 资助金额:
$ 2.09万 - 项目类别:
Cell-specific Modulation of Feeding Behavior by Serotonin 2C Receptor RNA Processing
5-羟色胺 2C 受体 RNA 加工对摄食行为的细胞特异性调节
- 批准号:
10438652 - 财政年份:2019
- 资助金额:
$ 2.09万 - 项目类别:
Cell-specific Modulation of Feeding Behavior by Serotonin 2C Receptor RNA Processing
5-羟色胺 2C 受体 RNA 加工对摄食行为的细胞特异性调节
- 批准号:
10000908 - 财政年份:2019
- 资助金额:
$ 2.09万 - 项目类别:
Novel transgenic tools for analysis of 5HT2C receptor expression and function
用于分析 5HT2C 受体表达和功能的新型转基因工具
- 批准号:
8433354 - 财政年份:2012
- 资助金额:
$ 2.09万 - 项目类别:
Novel transgenic tools for analysis of 5HT2C receptor expression and function
用于分析 5HT2C 受体表达和功能的新型转基因工具
- 批准号:
8299772 - 财政年份:2012
- 资助金额:
$ 2.09万 - 项目类别:
Project 5 Modulation and Function of 5HT2C Receptors
项目5 5HT2C受体的调节和功能
- 批准号:
8330304 - 财政年份:2011
- 资助金额:
$ 2.09万 - 项目类别:
POSTTRANSCRIPTIONAL REGULATION OF SEROTONIN RECEPTORS
5-羟色胺受体的转录后调节
- 批准号:
2038657 - 财政年份:1997
- 资助金额:
$ 2.09万 - 项目类别:
POSTTRANSCRIPTIONAL REGULATION OF SEROTONIN RECEPTORS
5-羟色胺受体的转录后调节
- 批准号:
2655549 - 财政年份:1997
- 资助金额:
$ 2.09万 - 项目类别:
Post-transcriptional Regulation of Serotonin Receptors
血清素受体的转录后调节
- 批准号:
6847988 - 财政年份:1997
- 资助金额:
$ 2.09万 - 项目类别: