首页> 外文期刊>Proceedings of the Japan Academy, Series B. Physical and Biological Sciences >Differential expression of DNA-dependent protein kinase catalytic subunit in the brain of neonatal mice and young adult mice
【24h】

Differential expression of DNA-dependent protein kinase catalytic subunit in the brain of neonatal mice and young adult mice

机译:新生儿小鼠脑中DNA依赖性蛋白激酶催化亚基的差异表达及幼年小鼠

获取原文
           

摘要

It is generally thought that younger people are more susceptible to cancer development after exposure to ionizing radiation in reference to epidemiological studies and animal experiments. However, little is known about the age-dependent alteration in DNA repair ability. In the present study, we examined the expression levels of proteins involved in the repair of DNA double-strand breaks through non-homologous end joining (NHEJ), i.e., DNA-dependent protein kinase catalytic subunit (DNA-PKcs), X-ray repair cross-complementing 4 (XRCC4) and XRCC4-like factor (XLF). We found that the expression of DNA-PKcs in brain tissues was higher in neonatal mice (1 week after birth) than in young adult mice (7 weeks after birth). In association with this, DNA double-strand breaks were repaired more rapidly in the brain tissues of neonatal mice than in those of young adult mice. The current results suggested a possible role for DNA-PKcs protecting developing brain tissues from DNA double-strand breaks.
机译:通常认为,在接触流行病学研究和动物实验后,暴露于电离辐射后,年轻人更容易受到癌症发育的影响。然而,关于DNA修复能力的年龄依赖性改变很少。在本研究中,我们检查了通过非同源末端接合(NHEJ),即DNA依赖性蛋白激酶催化亚基(DNA-PKC),X射线(DNA-PKC),X射线检查所涉及的DNA双链修复中所涉及的蛋白质的表达水平。修复交叉互补4(XRCC4)和XRCC4样因子(XLF)。我们发现,脑组织中DNA-PKCs的表达在新生儿小鼠(出生后1周)比年轻成年小鼠(出生后7周)较高。与此联合,在新生儿小鼠的脑组织中比在新生小鼠的脑组织中更快地修复DNA双链断裂。目前的结果表明DNA-PKCs保护从DNA双链断裂的发展脑组织的可能作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号