首页> 外文期刊>Scientific reports. >The K167I variant of DNA polymerase β that is found in Esophageal Carcinoma patients impairs polymerase activity and BER
【24h】

The K167I variant of DNA polymerase β that is found in Esophageal Carcinoma patients impairs polymerase activity and BER

机译:食管癌患者中发现的DNA聚合酶β的K167I变体损害聚合酶活性和BER

获取原文
           

摘要

DNA polymerase β (pol β) is a key enzyme in DNA base excision repair, and an important factor for maintaining genomic integrity and stability. Esophageal carcinoma (EC) patients who have been identified as carrying the K167I variant of pol β have been shown to have decreased life expectancy. However, it is unknown if the variant affects pol β’s functions and/or how it contributes to the initiation and progression of cancer. In this study, we expressed and purified the K167I variant. Moreover, we found that K167I significantly reduced polymerase activity. As a result, the K167I substitution reduced base excision repair (BER) efficiency when assayed in a reconstitution assay or when using cellular extracts. Finally, we observed EC cells expressing the K167I variant to be sensitive to DNA damaging agents. These results suggest the K167I variant affected pol β biochemical activity resulting in impaired BER function, which might subsequently contribute to genomic instability and cancer development.
机译:DNA聚合酶β(polβ)是DNA碱基切除修复中的关键酶,并且是维持基因组完整性和稳定性的重要因素。食道癌(EC)患者被鉴定为携带polβ的K167I变体,已显示出预期寿命的缩短。但是,尚不清楚该变体是否影响polβ的功能和/或它如何促进癌症的发生和发展。在这项研究中,我们表达并纯化了K167I变体。此外,我们发现K167I大大降低了聚合酶活性。结果,当在重组测定中或使用细胞提取物进行测定时,K167I取代降低了碱基切除修复(BER)的效率。最后,我们观察到表达K167I变体的EC细胞对DNA破坏剂敏感。这些结果表明,K167I变体影响了polβ的生化活性,从而导致BER功能受损,从而可能继而导致基因组不稳定和癌症发展。

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