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

被引:151
作者
Davies, W
Isles, A
Smith, R
Karunadasa, D
Burrmann, D
Humby, T
Ojarikre, O
Biggin, C
Skuse, D
Burgoyne, P
Wilkinson, L
机构
[1] Babraham Inst, Lab Cognit & Behav Neurosci, Cambridge CB2 4AT, England
[2] Babraham Inst, Lab Dev Genet & Imprinting, Cambridge CB2 4AT, England
[3] Natl Inst Med Res, MRC, Div Dev Genet, London NW7 1AA, England
[4] Inst Child Hlth, Behav Sci Unit, London WC1N 1EH, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/ng1577
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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(1). There is increasing evidence from mouse and human studies that imprinted genes may influence behavior and cognitive functioning(2). Previous work in girls with Turner syndrome (45,XO) has suggested that there are X-linked parent-of-origin effects on brain development(3) and cognitive functioning(4), although the interpretation of these data in terms of imprinted gene effects has been questioned(5). 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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页码:625 / 629
页数:5
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