GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ Twins.

IF 1 4区 医学 Q4 GENETICS & HEREDITY
Scott D Gordon, David L Duffy, David C Whiteman, Catherine M Olsen, Kerrie McAloney, Jessica M Adsett, Natalie A Garden, Simone M Cross, Susan E List-Armitage, Joy Brown, Jeffrey J Beck, Hamdi Mbarek, Sarah E Medland, Grant W Montgomery, Nicholas G Martin
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引用次数: 1

Abstract

Female fertility is a complex trait with age-specific changes in spontaneous dizygotic (DZ) twinning and fertility. To elucidate factors regulating female fertility and infertility, we conducted a genome-wide association study (GWAS) on mothers of spontaneous DZ twins (MoDZT) versus controls (3273 cases, 24,009 controls). This is a follow-up study to the Australia/New Zealand (ANZ) component of that previously reported (Mbarek et al., 2016), with a sample size almost twice that of the entire discovery sample meta-analysed in the previous article (and five times the ANZ contribution to that), resulting from newly available additional genotyping and representing a significant increase in power. We compare analyses with and without male controls and show unequivocally that it is better to include male controls who have been screened for recent family history, than to use only female controls. Results from the SNP based GWAS identified four genomewide significant signals, including one novel region, ZFPM1 (Zinc Finger Protein, FOG Family Member 1), on chromosome 16. Previous signals near FSHB (Follicle Stimulating Hormone beta subunit) and SMAD3 (SMAD Family Member 3) were also replicated (Mbarek et al., 2016). We also ran the GWAS with a dominance model that identified a further locus ADRB2 on chr 5. These results have been contributed to the International Twinning Genetics Consortium for inclusion in the next GWAS meta-analysis (Mbarek et al., in press).

在澳大利亚DZ双胞胎母亲的扩大样本中异卵双胞胎的GWAS。
女性生育能力是一种复杂的特征,随年龄的变化而发生异卵(DZ)双胞胎和生育能力。为了阐明调节女性生育能力和不孕症的因素,我们对自发性DZ双胞胎(MoDZT)的母亲与对照组(3273例,24009例对照)进行了全基因组关联研究(GWAS)。这是之前报道的澳大利亚/新西兰(ANZ)部分的后续研究(Mbarek等人,2016年),样本量几乎是上一篇文章中分析的整个发现样本荟萃分析的两倍(是ANZ贡献的五倍),这是由于新获得的额外基因分型,并且代表了显著的力量增加。我们比较了有和没有男性对照的分析,明确地表明,包括最近家族史筛查的男性对照比只使用女性对照更好。基于SNP的GWAS鉴定了4个全基因组显著信号,包括16号染色体上的一个新区域ZFPM1(锌指蛋白,FOG家族成员1)。FSHB(促卵泡激素β亚基)和SMAD3 (SMAD家族成员3)附近的先前信号也被复制(Mbarek et al., 2016)。我们还用显性模型进行了GWAS,在chr 5上发现了另一个ADRB2位点。这些结果已提交给国际双胞胎遗传学联合会,以便纳入下一个GWAS荟萃分析(Mbarek等人,已出版)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Twin Research and Human Genetics
Twin Research and Human Genetics 医学-妇产科学
CiteScore
1.50
自引率
11.10%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Twin Research and Human Genetics is the official journal of the International Society for Twin Studies. Twin Research and Human Genetics covers all areas of human genetics with an emphasis on twin studies, genetic epidemiology, psychiatric and behavioral genetics, and research on multiple births in the fields of epidemiology, genetics, endocrinology, fetal pathology, obstetrics and pediatrics. Through Twin Research and Human Genetics the society aims to publish the latest research developments in twin studies throughout the world.
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