Kohn Y, Lerer B
Department of Psychiatry, Biological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Mol Psychiatry. 2005 Dec;10(12):1062-73. doi: 10.1038/sj.mp.4001738.
The search for genes that are implicated in the pathogenesis of schizophrenia (SCZ), bipolar disorder (BPD) and other complex neuropsychiatric phenotypes has yielded a plethora of positive findings, but has also engendered a substantial degree of confusion. Exciting findings include positive linkage results in a number of chromosomal regions and the identification of several genes that have been associated with SCZ and to a lesser extent with BPD. Confusing aspects include the difference between studies in localization of linkage peaks in the same chromosomal regions, raising the possibility that these regions may harbor more than one gene, the fact that positive linkage findings as well as associated genes appear in several cases to be shared by more than one disorder, and the failure to identify thus far the precise pathogenic variants in associated genes. Recent findings of linkage and association studies on chromosome 6q illustrate the current status of neuropsychiatric genetics in intriguing microcosm. Positive findings from linkage and association studies are reviewed in order to identify approaches that may help to settle apparent contradictions and allow an interpretation of the results that may prove useful in application to findings from other chromosomal regions. Not only SCZ and BPD but also other psychiatric and neurological phenotypes are considered. Taking a topographic approach, we identify five foci of positive findings on chromosome 6q and suggest that each may harbor gene(s) that confer susceptibility to SCZ or BPD or may modify their onset or clinical course. We further suggest that in searching for these genes the possibility that they may be implicated in more than one disorder should be taken into account. We also discuss the potential contribution of rare genetic variants identified in homogeneous, isolated populations to the subsequent identification of common variants in the same gene that contribute to disease susceptibility in outbred populations.
对与精神分裂症(SCZ)、双相情感障碍(BPD)及其他复杂神经精神疾病表型发病机制相关基因的研究已取得了大量阳性结果,但也引发了相当程度的困惑。令人兴奋的发现包括在多个染色体区域获得的阳性连锁结果,以及鉴定出一些与SCZ相关且在较小程度上与BPD相关的基因。令人困惑的方面包括同一染色体区域连锁峰定位研究之间的差异,这增加了这些区域可能存在不止一个基因的可能性;在一些情况下,阳性连锁发现以及相关基因似乎为不止一种疾病所共有;以及迄今为止未能鉴定出相关基因中确切的致病变异。6号染色体长臂(6q)连锁和关联研究的最新发现以一种引人入胜的微观视角阐明了神经精神遗传学的现状。本文对连锁和关联研究的阳性结果进行了综述,以确定可能有助于解决明显矛盾并对结果做出解释的方法,这些解释可能对应用于其他染色体区域的研究结果有用。研究对象不仅包括SCZ和BPD,还包括其他精神和神经疾病表型。采用一种拓扑学方法,我们确定了6q染色体上五个阳性发现的焦点,并提出每个焦点可能包含赋予SCZ或BPD易感性或可能改变其发病或临床病程的基因。我们进一步提出,在寻找这些基因时,应考虑到它们可能与不止一种疾病相关的可能性。我们还讨论了在同质、隔离人群中鉴定出的罕见遗传变异对随后在远交人群中鉴定出导致疾病易感性的同一基因中的常见变异的潜在贡献。