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Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function | | D H Skuse
; R S James
; D V Bishop
; B Coppin
; P Dalton
; G Aamodt-Leeper
; M Bacarese-Hamilton
; C Creswell
; R McGurk
; P A Jacobs
; | | Date: |
12 Jun 1997 | | Journal: | Nature, 387 (6634), 705-8 | | Abstract: | Turner’s syndrome is a sporadic disorder of human females in which all or part of one X chromosome is deleted. Intelligence is usually normal but social adjustment problems are common. Here we report a study of 80 females with Turner’s syndrome and a single X chromosome, in 55 of which the X was maternally derived (45,X[m]) and in 25 it was of paternal origin (45,X[p]). Members of the 45,X[p] group were significantly better adjusted, with superior verbal and higher-order executive function skills, which mediate social interactions. Our observations suggest that there is a genetic locus for social cognition, which is imprinted and is not expressed from the maternally derived X chromosome. Neuropsychological and molecular investigations of eight females with partial deletions of the short arm of the X chromosome indicate that the putative imprinted locus escapes X-inactivation, and probably lies on Xq or close to the centromere on Xp. If expressed only from the X chromosome of paternal origin, the existence of this locus could explain why 46,XY males (whose single X chromosome is maternal) are more vulnerable to developmental disorders of language and social cognition, such as autism, than are 46,XX females. | | Source: | PubMed, pmid9192895 doi: 10.1038/42706 | | Services: | Forum | Review | Favorites | |
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