2001 CAG Triplet Repeat Disorders

2001 年 CAG 三联重复障碍

• 批准号: 6322057
• 负责人: PATRICK BRUNDIN
• 金额: $ 4万
• 依托单位: GORDON RESEARCH CONFERENCES
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-04-01 至 2002-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6322057
• 关键词: Friedreich's ataxia; Huntington's disease; fragile X syndromes; genetic disorder; meeting /conference /symposium; myotonic dystrophy; nervous system disorder; orphan disease /drug

This application is to request funding for the 2001 Gordon Research Conference on CAG triplet repeat disorders to be held in Mount Holyoke College, MA, USA, July 15-20, 2001. Two major groups of genetic neurological disorders were recently identified as unstable triplet repeat diseases. Their discovery represents the foundation of a new set of principles in genetics. One group of diseases includes fragile X, myotonic dystrophy and Friedreich's ataxia. Patients with these disorders all exhibit an expansion of triplet repeats in a non-coding sequence of the DNA genome. In the contrast, the other group of neurologic disorders exhibit expanded triplet repeats (coding for CAG bases) in the coding part of the genome, resulting in a polyglutamine tract. This latter group includes Huntington's disease, spino-cerebellar ataxia 1, 2, 3, 6 and 7, spinobulbar muscular atrophy and dentato-rubral pallido-luysian atrophy. These disorders results in a selective loss of neurons in the brain and spinal cord, with a different anatomical distribution in each disease. Although the genetic defects are established, it remains to be elucidated how the mutant gene in each case generates the specific pathogenetic process and how this leads to a characteristic anatomical pattern of changes. The identification of these mutant genes raises hopes for many affected by severe genetic disease. However, before development of novel therapies can be expected, it is necessary to better understand the disease processes. This requires a multi-disciplinary research effort with collaborative projects between scientists from diverse specialties ranging from fruit fly genetics to clinical neurology and neuropathology. This conference on CAG triplet repeat disorders will gather both young and senior, key scientists who will present provoking lectures on the cutting-edge of science. In keeping with the Gordon Research Conference format, there will be generous time allocated to both structured discussions led by peers and for informal discussions and social generous time allocated to both structured discussions led by peers and for informal discussions and social interaction. Strong emphasis is placed on training and mentoring of young scientists and time is also devoted to career issues. All participants (except speakers and discussants) will be encouraged to present posters. When participants are selected there will also be priority given to women, minorities, and persons with disabilities

本申请旨在为2001年7月15日至20日在美国马萨诸塞州芒特霍利奥克学院举行的2001年戈登CAG三联体重复紊乱研究会议申请资金。最近，两组主要的遗传性神经疾病被确认为不稳定的三联体重复疾病。他们的发现代表了一套新的遗传学原理的基础。一组疾病包括脆性X、强直性肌营养不良和弗里德里希共济失调。这些疾病的患者都表现出DNA基因组非编码序列中三联体重复序列的扩张。相比之下，另一组神经系统疾病在基因组的编码部分显示出扩大的三联体重复(编码CAG碱基)，导致多谷氨酰胺束。后一组包括亨廷顿病、脊髓-小脑性共济失调1、2、3、6和7、脊髓延髓肌萎缩和齿状红斑苍白球-鲁伊斯萎缩。这些疾病导致大脑和脊髓神经元的选择性丧失，在每种疾病中有不同的解剖分布。虽然基因缺陷已经确定，但突变基因如何在每种情况下产生特定的致病过程，以及如何导致特有的解剖变化模式，仍有待阐明。这些突变基因的识别为许多受到严重遗传病影响的人带来了希望。然而，在开发新的治疗方法之前，有必要更好地了解疾病的过程。这需要多学科的研究努力，需要来自不同专业的科学家之间的合作项目，从果蝇遗传学到临床神经学和神经病理学。这次关于CAG三联体重复紊乱的会议将聚集年轻和资深的关键科学家，他们将就科学的前沿发表引人入胜的演讲。按照戈登研究会议的形式，将为同行领导的结构化讨论和非正式讨论分配大量时间，为同行领导的结构化讨论和非正式讨论和社会互动分配大量社会时间。非常重视对年轻科学家的培训和指导，时间也花在职业问题上。将鼓励所有与会者(发言者和讨论者除外)展示海报。在选定参与者时，还将优先考虑妇女、少数群体和残疾人。