Crow T J, Delisi L E, Lofthouse R, Poulter M, Lehner T, Bass N, Shah T, Walsh C, Boccio-Smith A, Shields G
Division of Psychiatry, Northwick Park Hospital, Harrow, Middlesex, UK.
Br J Psychiatry. 1994 Feb;164(2):159-64. doi: 10.1192/bjp.164.2.159.
We investigated linkage between schizophrenia and the loci DXYS14, DXYS17, and MIC2 within the pseudoautosomal region in 85 families with two or more siblings suffering from schizophrenia or schizoaffective disorder. A maximum lod score of 2.44 was reached at MIC2, with a dominant model of inheritance at a recombination fraction of 0.367 in females and 0.046 in males (a F:M sex ratio > 1, i.e. opposite to that expected with a pseudoautosomal locus). Evidence consistent with linkage (P = 0.01) was also obtained with a sibling pair analysis at the MIC2 locus. These data do not support (although they do not definitively exclude) a locus within the pseudoautosomal region; they are consistent with the presence of a gene that predisposes to schizophrenia in the sex-specific regions of the X and Y chromosomes.
我们在85个有两个或更多患精神分裂症或分裂情感性障碍兄弟姐妹的家庭中,研究了精神分裂症与假常染色体区域内的DXYS14、DXYS17和MIC2基因座之间的连锁关系。在MIC2基因座处达到了最大对数优势分数2.44,在重组率为0.367时女性呈显性遗传模式,男性为0.046(F:M性别比>1,即与假常染色体基因座预期的相反)。在MIC2基因座进行同胞对分析时也获得了与连锁一致的证据(P = 0.01)。这些数据不支持(尽管没有明确排除)假常染色体区域内存在一个基因座;它们与X和Y染色体性别特异性区域中存在导致精神分裂症的基因一致。