...
首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Cytoplasmically sequestered wild-type p53 protein in neuroblastoma is relocated to the nucleus by a C-terminal peptide
【24h】

Cytoplasmically sequestered wild-type p53 protein in neuroblastoma is relocated to the nucleus by a C-terminal peptide

机译:神经母细胞瘤中被细胞质隔离的野生型p53蛋白通过C末端肽重新定位到细胞核

获取原文
获取原文并翻译 | 示例
           

摘要

Cytoplasmic sequestration of wild-type p53 protein occurs in a subset of primary human tumors including breast cancer, colon cancer, and neuroblastoma (NB). The sequestered p53 localizes to punctate cytoplasmic structures that represent large protein aggregates. One functional con- sequence of this blocked nuclear access is impairment of the p53-mediated G1 checkpoint after DNA damage. Here we show that cytoplasmic p53 from NB cells is incompetent for specific DNA binding, probably due to its sequestration.
机译:野生型p53蛋白的细胞质隔离发生在包括乳腺癌,结肠癌和神经母细胞瘤(NB)在内的原发性人类肿瘤的子集中。螯合的p53定位于代表大蛋白聚集体的点状细胞质结构。这种被阻止的核通路的功能性后果是DNA损伤后p53介导的G1检查点的损伤。在这里,我们显示来自NB细胞的胞质p53不适合特定的DNA结合,可能是由于其螯合。

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