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Heritability of DNA-damage-induced apoptosis and its relationship with age in lymphocytes from female twins

机译:双胞胎淋巴细胞中DNA损伤诱导的细胞遗传力及其与年龄的关系

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摘要

Apoptosis is a physiological form of cell death important in normal processes such as morphogenesis and the functioning of the immune system. In addition, defects in the apoptotic process play a major role in a number of important areas of disease, such as autoimmune diseases and cancer. DNA-damage-induced apoptosis plays a vital role in the maintenance of genomic stability by the removal of damaged cells. Previous studies of the apoptotic response (AR) to radiation-induced DNA damage of lymphoid cells from individuals carrying germline TP53 mutations have demonstrated a defective AR compared with normal controls. We have also previously demonstrated that AR is reduced as individuals age. Results from the current study on 108 twins aged 18–80 years confirm these earlier findings that the AR of lymphoid cells to DNA damage is significantly reduced with increasing age. In addition this twin study shows, for the first time, that DNA-damage-induced AR has a strong degree of heritability of 81% (95% confidence interval 67–89%). The vital role of DNA-damage-induced apoptosis in maintaining genetic stability, its relationship with age and its strong heritability underline the importance of this area of biology and suggest areas for further study.
机译:凋亡是细胞死亡的一种生理形式,在正常过程中非常重要,例如形态发生和免疫系统的功能。另外,凋亡过程中的缺陷在许多重要的疾病领域如自身免疫性疾病和癌症中起着重要作用。通过损伤细胞的去除,DNA损伤诱导的细胞凋亡在维持基因组稳定性中起着至关重要的作用。以前对携带种系TP53突变的个体对淋巴样细胞的辐射诱导的DNA损伤的凋亡反应(AR)的研究表明,与正常对照相比,AR有缺陷。先前我们还证明,随着年龄的增长,AR会降低。目前对108位年龄在18-80岁的双胞胎的研究结果证实了这些较早的发现,即随着年龄的增长,淋巴样细胞对DNA损伤的AR显着降低。此外,这项双生子研究首次表明,DNA损伤诱导的AR具有81%的高度遗传力(95%的置信区间67-89%)。 DNA损伤诱导的细胞凋亡在维持遗传稳定性,与年龄的关系及其强大的遗传力中起着至关重要的作用,突显了这一生物学领域的重要性,并提出了需要进一步研究的领域。

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