...
首页> 外文期刊>Oncogene >Merkel cell polyomavirus small T antigen induces genome instability by E3 ubiquitin ligase targeting
【24h】

Merkel cell polyomavirus small T antigen induces genome instability by E3 ubiquitin ligase targeting

机译:默克尔细胞多瘤病毒小T抗原通过E3泛素连接酶靶向诱导基因组不稳定

获取原文
           

摘要

The formation of a bipolar mitotic spindle is an essential process for the equal segregation of duplicated DNA into two daughter cells during mitosis. As a result of deregulated cellular signaling pathways, cancer cells often suffer a loss of genome integrity that might etiologically contribute to carcinogenesis. Merkel cell polyomavirus (MCV) small T (sT) oncoprotein induces centrosome overduplication, aneuploidy, chromosome breakage and the formation of micronuclei by targeting cellular ligases through a sT domain that also inhibits MCV large T oncoprotein turnover. These results provide important insight as to how centrosome number and chromosomal stability can be affected by the E3 ligase targeting capacity of viral oncoproteins such as MCV sT, which may contribute to Merkel cell carcinogenesis.
机译:双极有丝分裂纺锤体的形成是在有丝分裂过程中将复制的DNA均等地分离成两个子细胞的必不可少的过程。由于细胞信号通路的失控,癌细胞经常遭受基因组完整性的丧失,这可能在病因上有助于癌变。默克尔细胞多瘤病毒(MCV)小T(sT)癌蛋白通过通过sT域靶向细胞连接酶来诱导中心体过度复制,非整倍性,染色体断裂和微核的形成,这也抑制了MCV大T癌蛋白的更新。这些结果提供了关于病毒癌蛋白(例如MCV sT)的E3连接酶靶向能力如何影响中心体数目和染色体稳定性的重要见解,这可能有助于默克尔细胞癌变。

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