2007 CAG Triplet Repeat Disorders Gordon Conference

描述（由申请人提供）：本申请为2007年5月13-18日在法国奥索瓦Paul Langevin中心举行的CAG三重重复疾病戈登研究会议申请资金。这将是第四届CAG重复疾病戈登研究会议；第一届于2001年在蒙特霍利奥克学院举行，第二届于2003年5月在意大利巴尔加的伊尔乔科举行，第三届于2005年7月在蒙特霍利奥克学院举行。在过去的十年中，导致一组主要的遗传性神经系统疾病的突变被发现是CAG三联体重复扩增。到目前为止，这类疾病包括亨廷顿氏病、脊髓小脑共济失调1、2、3、6、7和17、脊髓和球性肌肉萎缩以及齿状脑白球性萎缩。在每种情况下，CAG重复位于基因的编码区，导致突变蛋白中异常长的聚谷氨酰胺束。基础遗传学和神经病理学的相似性表明，发病机制具有共同的特征。然而，这些疾病导致大脑和脊髓中选择性神经元损失的解剖分布不同，因此区分它们的因素也需要解开。由于遗传缺陷的鉴定，对这些疾病的发病机制有了重要的认识。这个领域已经发展到理性治疗学的发展不仅是在地平线上，而且已经发生了。为了加快基础研究的步伐，同时建立必要的联系和临床资源，将基础科学推向临床，需要多学科的研究努力。从有机化学、果蝇遗传学到临床神经学等不同专业的科学家之间建立合作项目是至关重要的。CAG三重重复障碍会议将聚集年轻的研究人员和资深科学家，就科学的前沿发表令人振奋的演讲。与戈登研究会议的形式保持一致，将有大量的时间分配给同行领导的结构化讨论和非正式讨论和社会互动，以促进合作。重点将放在对年轻科学家的培训和指导上，时间将用于职业问题。所有参与者都需要提交海报。在选择参加者时，将优先考虑妇女、少数民族和残疾人。

DESCRIPTION (provided by applicant): This application requests funding for the 2007 Gordon Research Conference on CAG Triplet Repeat Disorders to be held at Centre Paul Langevin, Aussois, France from May 13-18, 2007. This will be the fourth Gordon Research Conference on CAG repeat disorders; the first was held in 2001 at Mount Holyoke College, the second was held in Il Ciocco, Barga, Italy in May 2003, and the third was held again at Mount Holyoke College in July 2005. During the last decade, the mutation that causes a major group of inherited neurological disorders was found to be a CAG triplet repeat expansion. So far, this group of diseases includes Huntington's disease, the spinocerebellar ataxias 1, 2, 3, 6, 7, and 17, spinal and bulbar muscular atrophy and dentatorubral pallidoluysian atrophy. In each case, the CAG repeat lies within the coding region of the gene and results in an abnormally long polyglutamine tract in the mutant protein. Similarities in the underlying genetics and neuropathology suggest that the mechanisms of pathogenesis share common features. However, these diseases result in different anatomical distributions of the selective loss of neurons in the brain and spinal cord, and therefore the factors that distinguish them also need to be unraveled. Since the identification of the genetic defects, significant insights have been gained into the pathogenesis of these diseases. The field has progressed to the extent that the development of rational therapeutics is not only on the horizon but is already occurring. In order to increase the pace of the basic research, and at the same time set in place the contacts and clinical resources necessary to move the basic science into the clinic, a multidisciplinary research effort is required. It is essential that collaborative projects between scientists from diverse specialties ranging from organic chemistry, fruit fly genetics to clinical neurology can be established. The conference on CAG triplet repeat disorders will gather together young investigators and established senior scientists to deliver provoking lectures on the cutting-edge of science. In keeping with the Gordon Research Conference format, there will be generous time allocated for both structured discussions led by peers and for informal discussions and social interactions to facilitate collaborations. Strong emphasis is placed on training and mentoring of young scientists, and time will be devoted to career issues. All participants will be required to present posters. Priority will be given to women, minorities, and persons with disabilities when selecting participants.