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Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth

机译:端粒长度与21号染色体不分离的类型有关:对唐氏综合症出生的母亲年龄影响的新见解

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Advanced maternal age is a well-documented risk factor of chromosome 21 nondisjunction in humans, but understanding of this association at the genetic level is still limited. In particular, the state of maternal genetic age is unclear. In the present study, we estimated maternal genetic age by measuring telomere length of peripheral blood lymphocytes among age-matched mothers of children with Down syndrome (cases: N = 75) and mothers of euploid children (controls: TV = 75) in an age range of 18-42 years. All blood samples were taken within 1 week of the birth of the child in both cases and controls. The telomere length estimation was performed by restriction digestion-Southern blot hybridization method. We stratified the cases on the basis of centromeric STR genotyping into maternal meiosis I (./V=48) and maternal meiosis II (N = 27) nondisjunction groups and used linear regression to compare telomere length as a function of age in the euploid, meiosis I and meiosis II groups. Our results show that all three groups have similar telomere length on average for younger mothers. As age increases, all groups show telomere loss, but that loss is largest in the meiosis II mother group and smallest in the euploid mother group with the meiosis I mother group in the middle. The regression lines for all three were statistically significantly different from each other (p < 0.001). Our results do not support the theory that younger women who have babies with Down syndrome do so because are 'genetically older' than their chronological age, but we provide the first evidence that older mothers who have babies with Down syndrome are "genetically older" than controls, who have euploid babies at the same age. We also show for the first time that telomere length attrition may be associated in some way with meiosis I and meiosis II nondisjunction of chromosome 21 and subsequent Down syndrome births at advanced maternal age.
机译:产妇高龄是人类21号染色体不分离的一个有据可查的危险因素,但在遗传水平上对这种关联的了解仍然有限。特别是,孕产妇遗传年龄的状态尚不清楚。在本研究中,我们通过测量年龄相匹配的唐氏综合症儿童(病例:N = 75)和整倍体儿童母亲(对照:TV = 75)的年龄相匹配的母亲外周血淋巴细胞的端粒长度,估算了母亲的遗传年龄。范围为18-42岁。无论是在病例还是对照中,所有血液样本均在孩子出生后的1周内采集。通过限制性消化-Southern印迹杂交法进行端粒长度估计。我们根据中心体STR基因分型将病例分层,分为母系减数分裂I(./V=48)和母体减数分裂II(N = 27)非分离组,并使用线性回归比较端粒长度与整倍体年龄的关系,减数分裂I和减数分裂II组。我们的结果表明,对于年轻母亲而言,所有三个组的端粒长度平均相似。随着年龄的增长,所有组均显示端粒丢失,但该丢失在减数分裂II型母亲组中最大,而在整倍体母亲组中最小,减数分裂I型母亲组在中间。这三个变量的回归线在统计学上均显着不同(p <0.001)。我们的结果不支持这样的理论,即患有唐氏综合症的婴儿的年轻女性之所以这样做是因为其“遗传上”比其年龄大,但我们提供的第一个证据表明,患有唐氏综合症的婴儿的年龄较大的母亲“比其年龄大”。对照,他们在同一年龄有整倍体婴儿。我们还首次显示端粒长度的减损可能与21号染色体的减数分裂I和减数分裂II不分离以及以后的高龄孕妇唐氏综合症有某种联系。

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