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The chemokine (C-C-motif) receptor 3 (CCR3) gene is linked and associated with age at menarche in Caucasian females

机译:趋化因子(C-C-基序)受体3(CCR3)基因与白人女性初潮年龄相关并相关

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摘要

Chemokine (C-C-motif) receptor 3 (CCR3), playing an important role in endometrium related metabolic pathways, may influence the onset of menarche. To test linkage and/or association between CCR3 polymorphisms with the variation of age at menarche (AAM) in Caucasian females, we recruited a sample of 1,048 females from 354 Caucasian nuclear families and genotyped 16 SNPs spanning the entire CCR3 gene. Linkage disequilibrium and haplotype blocks were inferred by Haploview. Both single-SNP markers and haplotypes were tested for linkage and/or association with AAM using QTDT (quantitative transmission disequilibrium test). We also tested associations between CCR3 polymorphisms and AAM in a selected random sample of daughters using ANOVA (analysis of variance). We identified two haplotype blocks. Only block two showed significant results. After correction for multiple testing, significant total associations of SNP7, SNP9 with AAM were detected (P = 0.009 and 0.006, respectively). We also detected significant within-family association of SNP9 (P = 0.01). SNP14 was linked to AAM (P = 0.02) at the nominal level. In addition, there was evidence of significant total association and nominal significant linkage (P = 0.008 and 0.03, respectively) with AAM for the haplotype AGA reconstructed by SNP7, SNP9 and SNP13. ANOVA confirmed the results by QTDT. For the first time we reported that CCR3 is linked and associated with AAM variation in Caucasian women. However, further studies are necessary to substantiate our conclusions.
机译:趋化因子(C-C-基序)受体3(CCR3)在子宫内膜相关的代谢途径中起重要作用,可能会影响月经初潮的发生。为了测试CCR3多态性与白人女性月经初潮(AAM)年龄之间的联系和/或关联,我们从354个白人核心家庭中招募了1,048名女性样本,并对16个SNP进行了基因分型,涉及整个CCR3基因。 Haploview推断出连锁不平衡和单体型模块。使用QTDT(定量传递不平衡测试)测试了单SNP标记和单倍型与AAM的连锁和/或缔合。我们还使用ANOVA(方差分析)在选定的女儿随机样本中测试了CCR3多态性与AAM之间的关联。我们确定了两个单元型模块。仅第二块显示了显着结果。经过多次测试校正后,检测到SNP7,SNP9与AAM的显着总关联(分别为P = 0.009和0.006)。我们还发现SNP9的家庭内部显着关联(P = 0.01)。 SNP14在名义水平上与AAM(P = 0.02)关联。此外,有证据表明,由SNP7,SNP9和SNP13重建的单倍型AGA与AAM具有显着的总关联和名义上的显着联系(分别为P = 0.008和0.03)。方差分析通过QTDT确认了结果。我们首次报道,CCR3与白人女性的AAM变异相关并相关。但是,需要进一步的研究来证实我们的结论。

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  • 来源
    《Human Genetics》 |2007年第1期|35-42|共8页
  • 作者单位

    Laboratory of Molecular and Statistical Genetics College of Life Sciences Hunan Normal University Changsha Hunan 410081 People’s Republic of China;

    Osteoporosis Research Center and Department of Biomedical Sciences Creighton University Omaha NE 68131 USA;

    The Key Laboratory of Biomedical Information Engineering of Ministry of Education and Institute of Molecular Genetics School of Life Science and Technology Xi’an Jiaotong University Xi’an 710049 People’s Republic of China;

    Osteoporosis Research Center and Department of Biomedical Sciences Creighton University Omaha NE 68131 USA;

    Osteoporosis Research Center and Department of Biomedical Sciences Creighton University Omaha NE 68131 USA;

    The Key Laboratory of Biomedical Information Engineering of Ministry of Education and Institute of Molecular Genetics School of Life Science and Technology Xi’an Jiaotong University Xi’an 710049 People’s Republic of China;

    Laboratory of Molecular and Statistical Genetics College of Life Sciences Hunan Normal University Changsha Hunan 410081 People’s Republic of China;

    Osteoporosis Research Center and Department of Biomedical Sciences Creighton University Omaha NE 68131 USA;

    Laboratory of Molecular and Statistical Genetics College of Life Sciences Hunan Normal University Changsha Hunan 410081 People’s Republic of China;

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  • 入库时间 2022-08-18 01:51:34

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