Schizophrenia as variation in the sapiens-specific epigenetic instruction to the embryo

作者：Crow T J^*

来源：Clinical Genetics, 2012, 81(4): 319-324.

DOI：10.1111/j.1399-0004.2012.01830.x

• bipolar disorder
• cerebral torque
• chromosome pairing
• epigenesis
• hominin lineage
• meiosis
• missing heritability
• MSUC
• PCDH11XY
• PRDM9
• sapiens
• schizophrenia
• sexual selection
• speciation
• Xq21
• 3
• Yp11
• 2

The psychoses (schizophrenia and bipolar disorder) occur in all populations with approximately uniform incidence and sex-dependent age of onset. Core symptoms involve aspects of language; brain structural deviations are sex and hemisphere-related. Genetic predisposition is unaccounted for by linkage or association. The hypothesis is proposed that the ` missing heritability' is epigenetic in form and generated in meiosis on a species-specific XY chromosomal template. A duplication from Xq21.3 to Yp11.2 that occurred 6 million years ago is proposed as critical to hominin evolution. Within this block of homology the Protocadherin11XY gene pair is expressed as a cell surface adhesion factor in both X and Y forms; it has undergone a series of coding changes (16 in the Y sequence and 5 in the X including two to cysteines) in the hominin lineage. According to the hypothesis these sequence changes, together with one or more deletions and a paracentric inversion in the Y block, were successively selected; late events in this series established cerebral asymmetry (the ` torque') as the defining characteristic of the human brain. Built around this reference frame, an epigenetic message channels early development of the embryo in a sapiens-specific format. Diversity in meiotic pairing is postulated as the basis for species-specific deviations in development associated with psychosis.

• 出版日期2012-4