Crow Timothy J
SANE POWIC, University Department of Psychiatry, Warneford Hospital, Oxford OX3 7JX, United Kingdom.
Schizophr Res. 2008 Jul;102(1-3):31-52. doi: 10.1016/j.schres.2008.03.010. Epub 2008 May 23.
To achieve a unified concept of the aetiology of psychosis.
The nuclear symptoms of "schizophrenia" occur with approximately the same age- and sex-specific incidence in all human populations. No substantive environmental precipitant has been identified, and yet these "illnesses" are associated with deviations in brain structure that are uniform across populations, are established late in development and relate to the capacity for language. No genes have been identified by linkage or association strategies.
It is postulated that the variation 1. relates precisely to the genetic mechanism that distinguishes the species Homo sapiens from its precursor. 2. constitutes a class of epigenetic diversity intrinsic to the genetic control of the species characteristic (the "specific mate recognition system" according to the theory of HEH Paterson). 3. reflects the role of the cerebral torque in the neuro-developmental re-organization that enabled the faculty of language. A genetic mechanism involving both the X and the Y chromosomes is suggested by 1) evidence for anomalies of asymmetry of brain structure and function in the sex chromosome aneuploidies, 2) a same sex concordance effect for handedness, 3) sex differences in lateralization, and verbal and spatial ability, and their inter-relationships. These three facts direct attention to the Xq21.3/Yp11.2 homology block that was established by an X to Y duplication 6 million years ago, ie at the time of origin of the hominid lineage. Within this block a gene pair (Protocadherin11X and Y) expressed as two cell surface adhesion molecules at axo-dendritic synapses has been subject to change (16 amino-acid substitutions in the Y, and critically 5 in the X sequence) in the hominid lineage. The X to Y duplication and its subsequent modification (4 deletions and a paracentric inversion) on the Y may have played a central role in hominid speciation with the most recent change (at around 160,000 years) representing the transition to language and modern Homo sapiens (the 'big bang'). The expression of genes within the homologous region is influenced by the extent to which the X and Y chromosomes pair in male meiosis (referred to as MSUC "meiotic suppression of unpaired chromosomes"). This mechanism generates epigenetic diversity relating to the species capacity for language; it is proposed as the basis of the genetic predisposition to psychosis.
Language and psychosis have a common origin in the genetic event (the 'big bang') that defined the species.
实现对精神病病因学的统一认识。
“精神分裂症”的核心症状在所有人群中出现的年龄和性别特异性发病率大致相同。尚未确定实质性的环境诱发因素,但这些“疾病”与全人群中一致的脑结构偏差有关,这些偏差在发育后期形成且与语言能力相关。通过连锁或关联策略尚未确定相关基因。
假定这种变异1. 精确地与将智人与其前身区分开来的遗传机制相关。2. 构成了物种特征遗传控制中固有的一类表观遗传多样性(根据HEH帕特森的理论为“特异性配偶识别系统”)。3. 反映了脑扭矩在实现语言能力的神经发育重组中的作用。涉及X和Y染色体的遗传机制由以下几点表明:1)性染色体非整倍体中脑结构和功能不对称异常的证据;2)利手的同性一致性效应;3)偏侧化、语言和空间能力的性别差异及其相互关系。这三个事实将注意力引向600万年前通过X向Y的复制而形成的Xq21.3/Yp11.2同源区段,即在人科谱系起源之时。在这个区段内,一对基因(原钙黏蛋白11X和Y)在轴突 - 树突突触处作为两种细胞表面黏附分子表达,在人科谱系中发生了变化(Y中有16个氨基酸替换,关键的是X序列中有5个)。X向Y的复制及其随后在Y上的修饰(4次缺失和1次臂间倒位)可能在人科物种形成中起了核心作用,最近的一次变化(约16万年前)代表了向语言和现代智人的转变(“大爆炸”)。同源区域内基因的表达受雄性减数分裂中X和Y染色体配对程度的影响(称为MSUC“未配对染色体的减数分裂抑制”)。这种机制产生了与物种语言能力相关的表观遗传多样性;它被提议作为精神病遗传易感性的基础。
语言和精神病在定义该物种的遗传事件(“大爆炸”)中有共同起源。