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Parental Effect of DNA (Cytosine-5) Methyltransferase 1 on Grandparental-Origin-Dependent Transmission Ratio Distortion in Mouse Crosses and Human Families

机译:DNA(Cytosine-5)甲基转移酶1对小鼠杂交和人类家庭中祖父母-原始依赖性传递比率失真的父母效应

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摘要

Transmission ratio distortion (TRD) is a deviation from the expected Mendelian 1:1 ratio of alleles transmitted from parents to offspring and may arise by different mechanisms. Earlier we described a grandparental-origin-dependent sex-of-offspring-specific TRD of maternal chromosome 12 alleles closely linked to an imprinted region and hypothesized that it resulted from imprint resetting errors in the maternal germline. Here, we report that the genotype of the parents for loss-of-function mutations in the Dnmt1 gene influences the transmission of grandparental chromosome 12 alleles. More specifically, maternal Dnmt1 mutations restore Mendelian transmission ratios of chromosome 12 alleles. Transmission of maternal alleles depends upon the presence of the Dnmt1 mutation in the mother rather than upon the Dnmt1 genotype of the offspring. Paternal transmission mirrors the maternal one: live-born offspring of wild-type fathers display 1:1 transmission ratios, whereas offspring of heterozygous Dnmt1 mutant fathers tend to inherit grandpaternal alleles. Analysis of allelic transmission in the homologous region of human chromosome 14q32 detected preferential transmission of alleles from the paternal grandfather to grandsons. Thus, parental Dnmt1 is a modifier of transmission of alleles at an unlinked chromosomal region and perhaps has a role in the genesis of TRD.
机译:传播比率畸变(TRD)与从父母传递给后代的等位基因的预期孟德尔1:1比率存在偏差,并且可能由不同的机制引起。早先,我们描述了与印记区域紧密相连的母本染色体12等位基因的祖父母起源后代性别特异性TRD,并假设它是由母本种系中的印记重置错误引起的。在这里,我们报告为Dnmt1基因功能丧失突变的父母的基因型影响祖父母12号染色体等位基因的传递。更具体地说,母体Dnmt1突变可恢复12号染色体等位基因的孟德尔传递比率。母体等位基因的传播取决于母亲中Dnmt1突变的存在,而不取决于后代的Dnmt1基因型。父本传播反映了母本:野生型父亲的活产后代显示出1:1的传播比率,而杂合Dnmt1突变父亲的后代倾向于遗传祖父等位基因。分析人染色体14q32同源区域中的等位基因传播,可以检测到等位基因从祖父到孙子的优先传播。因此,亲本Dnmt1是等位基因在未连接的染色体区域的传递的修饰子,可能在TRD的发生中起作用。

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