Literature DB >> 15908950

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice.

William Davies1, Anthony Isles, Rachel Smith, Delicia Karunadasa, Doreen Burrmann, Trevor Humby, Obah Ojarikre, Carol Biggin, David Skuse, Paul Burgoyne, Lawrence Wilkinson.   

Abstract

Imprinted genes show differential expression between maternal and paternal alleles as a consequence of epigenetic modification that can result in 'parent-of-origin' effects on phenotypic traits. There is increasing evidence from mouse and human studies that imprinted genes may influence behavior and cognitive functioning. Previous work in girls with Turner syndrome (45,XO) has suggested that there are X-linked parent-of-origin effects on brain development and cognitive functioning, although the interpretation of these data in terms of imprinted gene effects has been questioned. We used a 39,XO mouse model to examine the influence of the parental origin of the X chromosome on cognitive behaviors and expression of X-linked genes in brain. Our findings confirm the existence of X-linked imprinted effects on cognitive processes and identify a new maternally expressed imprinted gene candidate on the X chromosome, Xlr3b, which may be of importance in mediating the behavioral effects.

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Year:  2005        PMID: 15908950     DOI: 10.1038/ng1577

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  75 in total

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Review 7.  Mouse model systems to study sex chromosome genes and behavior: relevance to humans.

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8.  XY sex chromosome complement, compared with XX, in the CNS confers greater neurodegeneration during experimental autoimmune encephalomyelitis.

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