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DNA(胞嘧啶-5)甲基转移酶1对小鼠杂交和人类家庭中祖父母来源依赖性传递比率畸变的亲本效应。

Parental effect of DNA (Cytosine-5) methyltransferase 1 on grandparental-origin-dependent transmission ratio distortion in mouse crosses and human families.

作者信息

Yang Lanjian, Andrade Moises Freitas, Labialle Stephane, Moussette Sanny, Geneau Geneviève, Sinnett Donna, Belisle Alexandre, Greenwood Celia M T, Naumova Anna K

机构信息

Department of Human Genetics, Faculty of Medicine, McGill University Montreal, Quebec, Canada.

出版信息

Genetics. 2008 Jan;178(1):35-45. doi: 10.1534/genetics.107.081562.

Abstract

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.

摘要

传递比率失真(TRD)是指从父母传递给后代的等位基因偏离预期的孟德尔1:1比率,可能由不同机制引起。此前我们描述了与一个印记区域紧密连锁的母本12号染色体等位基因存在依赖祖父母起源的后代性别特异性TRD,并推测这是由母本生殖系中的印记重置错误导致的。在此,我们报告Dnmt1基因功能丧失突变的亲本基因型会影响祖父母12号染色体等位基因的传递。更具体地说,母本Dnmt1突变可恢复12号染色体等位基因的孟德尔传递比率。母本等位基因的传递取决于母亲中Dnmt1突变的存在,而非后代的Dnmt1基因型。父本传递与母本传递情况相似:野生型父亲的活产后代显示1:1的传递比率,而异合子Dnmt1突变型父亲的后代倾向于继承祖父的等位基因。对人类染色体14q32同源区域的等位基因传递分析检测到从祖父到孙子的等位基因优先传递。因此,亲本Dnmt1是一个未连锁染色体区域上等位基因传递的修饰因子,可能在TRD的发生中起作用。

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