Naumova A K, Olien L, Bird L M, Slamka C, Fonseca M, Verner A E, Wang M, Leppert M, Morgan K, Sapienza C
Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Dev Genet. 1995;17(3):198-205. doi: 10.1002/dvg.1020170304.
We have begun a search for heritable variation in X-chromosome inactivation pattern in normal females to determine whether there is a genetic effect on the imprinting of X-chromosome inactivation in humans. We have performed a quantitative analysis of X-chromosome inactivation in lymphocytes from mothers in normal, three-generation families. Eight mothers and 12 grandmothers exhibited evidence of highly skewed patterns of X-chromosome inactivation. We observed that the male offspring of females with skewed X-inactivation patterns were three times more likely to inherit alleles at loci that were located on the inactive X chromosome (Xi) than the active X chromosome (Xa). The region of the X chromosome for which this phenomenon was observed extends from Xp11 to -Xq22. We have also examined X-chromosome inactivation patterns in 21 unaffected mothers of male bilateral sporadic retinoblastoma patients. Six of these mothers had skewed patterns of X-chromosome inactivation. In contrast to the tendency for male offspring of skewed mothers from nondisease families to inherit alleles from the inactive X chromosome, five of the six affected males inherited the androgen receptor alleles from the active X chromosome of their mother.
我们已开始在正常女性中寻找X染色体失活模式的可遗传变异,以确定人类X染色体失活的印记是否存在遗传效应。我们对来自正常三代家庭中母亲淋巴细胞的X染色体失活进行了定量分析。8位母亲和12位祖母表现出X染色体高度偏态失活模式的证据。我们观察到,X染色体失活模式偏态的女性的男性后代在位于失活X染色体(Xi)上的基因座继承等位基因的可能性是位于活性X染色体(Xa)上的三倍。观察到这种现象的X染色体区域从Xp11延伸至-Xq22。我们还检查了21名男性双侧散发性视网膜母细胞瘤患者未受影响的母亲的X染色体失活模式。其中6位母亲有X染色体偏态失活模式。与非疾病家庭中失活模式偏态的母亲的男性后代倾向于从失活X染色体继承等位基因不同,这6名受影响男性中的5名从其母亲的活性X染色体继承了雄激素受体等位基因。