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The known genetic loci for telomere length may be involved in the modification of telomeres length after birth

机译:用于端粒长度的已知遗传基因座可参与出生后立端性长度的修饰

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Telomere length varies considerably among individuals. It is highly heritable and decreases with ageing or ageing related diseases. Recently, genome-wide association studies (GWAS) have identified several genetic loci associated with telomere length in adults. However, it is unclear whether these loci represent the genetic basis of telomere length or determine the individual susceptibility to shortening during growth process. Using DNA extracted from peripheral and cord blood of 444 mother-newborn pairs from a Chinese population, we measured relative telomere length (RTL) and genotyped eight known telomere length related variants that were initially identified in populations of European descent. We observed the T allele of rs10936599 and the T allele of rs2736100 were norminally associated with shorter RTL (P?=?0.041 and 0.046, respectively) in maternal samples. Furthermore, the Weighted genetic score (WGS) of eight variants was significantly associated with RTL in maternal samples (R(2)?=?0.012, P?=?0.025). However, we didn't detect any significant associations for any individual variant or the combined WGS with RTL in newborns. These findings didn't support the hypothesis that telomere length related loci may affect telomere length at birth, and we suggested that these loci may play a role in telomere length modification during life course.
机译:端粒长度在个人之间变化很大。随着衰老或衰老的相关疾病是高度遗传和降低。最近,基因组 - 宽协会研究(GWAS)已经确定了几种与成人端粒长度相关的遗传基因座。然而,目前尚不清楚这些基因座是否代表端粒长度的遗传基础,或者确定在生长过程中对缩短的个体易感性。使用从中国人群的444母新生儿对的外周血和脐带血中提取的DNA,我们测量了相对端粒长度(RTL)和基因分型的八个已知的端粒长度相关变体,最初在欧洲血统的群体中鉴定。我们观察到RS10936599的T等位基因,RS2736100的T等位基因常与母体样品中的rTL(P?= 0.041和0.046分别)。此外,八个变体的加权遗传分数(WGS)与母体样品中的RTL显着相关(R(2)?=Δ= 0.012,p?= 0.025)。然而,我们没有检测到任何单独变体或与新生儿的RTL组合的WG的任何重要关联。这些发现并不支持那些端粒长度相关基因座可能影响出生时的端粒长度的假设,我们建议这些基因座可能在生命过程中以端粒长度修改发挥作用。

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