Sabl J F, Laird C D
Department of Zoology, University of Washington, Seattle 98195.
Am J Hum Genet. 1992 Jun;50(6):1171-7.
Epigenetic modification of DNA is now recognized as a potentially important factor in the inheritance and expression of some mutations; its ability to complicate human genetic analysis is concurrently becoming apparent. One unusual form of epigenetic modification, dominant position-effect variegation (PEV), has been used as a model for Huntington disease. In dominant PEV, a fully dominant mutant phenotype results from stable epigenetic inactivation of an allele adjacent to the structural alteration (cis-inactivation) combined with a complementary inactivation of the homologous normal allele (trans-inactivation). We now propose that trans-inactivation of the normal allele may occasionally persist through meiosis. Such "epigene conversion" occurring at the Huntington disease locus in a few percent of meioses would largely account for the published anomalies in that region's genetic map. This concept could also explain anomalous linkage map data for other disease-causing alleles in humans.
DNA的表观遗传修饰如今被认为是某些突变的遗传和表达中一个潜在的重要因素;其使人类遗传分析复杂化的能力也正日益显现。一种不寻常的表观遗传修饰形式,即显性位置效应斑驳(PEV),已被用作亨廷顿病的模型。在显性PEV中,完全显性的突变表型源于与结构改变相邻的等位基因的稳定表观遗传失活(顺式失活),并伴有同源正常等位基因的互补失活(反式失活)。我们现在提出,正常等位基因的反式失活偶尔可能会通过减数分裂持续存在。在少数减数分裂中发生在亨廷顿病基因座的这种“表观基因转换”,将很大程度上解释该区域遗传图谱中已公布的异常情况。这一概念也可以解释人类其他致病等位基因的异常连锁图谱数据。