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

被引:10
|
作者
Yang, Lanjian [1 ]
Andrade, Moises Freitas [2 ,3 ]
Labialle, Stephane [2 ,3 ]
Moussette, Sanny [2 ,3 ]
Geneau, Genevive [4 ,5 ]
Sinnett, Donna [4 ,5 ]
Belisle, Alexandre [4 ,5 ]
Greenwood, Celia M. T. [6 ,7 ]
Naumova, Anna K. [1 ,2 ,3 ]
机构
[1] McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ H3A 1B1, Canada
[2] McGill Univ, Fac Med, Dept Obstet & Gynecol, Montreal, PQ H3A 1B1, Canada
[3] McGill Univ, Res Inst, Ctr Hlth, Montreal, PQ H3A 1B1, Canada
[4] McGill Univ, Montreal, PQ H3A 1A4, Canada
[5] Genome Quebec Innovat Ctr, Montreal, PQ H3A 1A4, Canada
[6] Hosp Sick Children, Res Inst, Program Genet & Genome Biol, Toronto, ON M5G 1L7, Canada
[7] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON M5T 3M7, Canada
关键词
D O I
10.1534/genetics.107.081562
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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 Dnnal 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.
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收藏
页码:35 / 45
页数:11
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