PLEIOTROPIC EFFECTS OF GENES LINKED TO SCHIZOPHRENIA

与精神分裂症相关的基因的多效性

• 批准号: 7032078
• 负责人: DEBORAH L LEVY
• 金额: $ 60.8万
• 依托单位: MCLEAN HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-02-01 至 2010-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7032078
• 关键词: behavioral genetics; clinical research; family genetics; gene expression; genetic markers; genetic screening; genetic susceptibility; human subject; linkage mapping; method development; molecular genetics; pleiotropism; schizophrenia; statistics /biometry

DESCRIPTION (provided by applicant): For many years this laboratory has focused intensively on characterizing schizophrenia-related traits (SRTs) as qualitative and quantitative phenotypes for schizophrenia. Three of these SRTs - thought disorder with schizophrenic features, eye tracking dysfunction and a craniofacial anomaly involving the frontonasal-maxilllary junction - stand out as especially probative for clarifying the neurobiological interpretation of schizophrenia susceptibility loci. Each of these traits has a much higher recurrence in relatives of schizophrenics than in schizophrenics. Moreover, unlike schizophrenia, which is generally thought to involve a number of co-acting genes, the family data on the SRTs are consistent with monogenic transmission models, and may therefore clarify the complex genetics of schizophrenia. The massive investment by NIMH in searching for genes for schizophrenia has resulted in an impressive number of promising candidate genes and chromosomal regions. Our progress in characterizing SRTs places us in an ideal position to determine whether any of these SRTs is linked to identified genes and "warm spot" regions for schizophrenia. We recognize, of course, that not all of the reported linkages will be replicable, but the probability is high that some of them are authentic, and the added cost of taking an inclusive view of the candidate loci is modest. Our power analyses show that the density of individuals affected with the SRTs in families of a schizophrenic proband is sufficiently high that, given a candidate locus associated with the SRT, the probability of our being able to detect that relationship is very high. If any of the genetic loci that have been linked to schizophrenia can be shown to be linked to any of the SRTs, it would open the way for building a neurobiological bridge between the disease phenotype and its genetic underpinnings, and it would add considerably to the confidence one can have in the reported linkages. Because of our laboratory's long involvement in investigating schizophrenia-related traits, the substantial number of families already acquired and thoroughly studied with respect to these traits and the expertise of our statistical and molecular genetics collaborators, our laboratory is uniquely positioned to carry out these studies.

描述（由申请人提供）：多年来，该实验室一直专注于将精神分裂症相关性状（SRT）作为精神分裂症的定性和定量表型。其中三个SRT-思维障碍与精神分裂症的特点，眼跟踪功能障碍和颅面异常涉及额鼻-上颌交界处-站出来，特别是证明澄清精神分裂症易感基因座的神经生物学解释。这些特征中的每一个在精神分裂症患者的亲属中的复发率都比精神分裂症患者高得多。此外，与精神分裂症，这通常被认为是涉及一些共同作用的基因，SRT的家庭数据与单基因传播模型是一致的，因此可能澄清精神分裂症的复杂遗传学。NIMH在寻找精神分裂症基因方面的大量投资已经产生了令人印象深刻的有希望的候选基因和染色体区域。我们在表征SRT方面的进展使我们处于一个理想的位置，以确定这些SRT中的任何一个是否与已识别的基因和精神分裂症的“热点”区域有关。当然，我们认识到，并非所有已报道的连锁都是可复制的，但其中一些连锁是真实的可能性很高，并且对候选基因座采取包容性观点的额外成本是适度的。我们的力量分析表明，密度的个人影响与SRT在家庭中的精神分裂症先证者是足够高的，给定的候选位点与SRT，我们能够检测到这种关系的概率是非常高的。如果任何与精神分裂症相关的基因位点都能被证明与任何一种SRT相关，这将为在疾病表型及其遗传基础之间建立神经生物学桥梁开辟道路，并将大大增加人们对所报道的联系的信心。由于我们实验室长期参与调查精神分裂症相关性状，大量家庭已经获得并彻底研究了这些性状以及我们统计和分子遗传学合作者的专业知识，我们实验室具有独特的优势来开展这些研究。