Pold4 is dispensable for mouse development, DNA replication and DNA repair

文献类型： 外文期刊

第一作者： Gu, Xueping

作者： Gu, Xueping;Dai, Qinjin;Du, Peng;Li, Ning;Li, Jiahui;Zeng, Simiao;Peng, Shuyi;Tang, Shengjun;Zhou, Zhongcheng;Wang, Lei

作者机构：

关键词： Pold4; DNA replication; DNA damage; DNA repair; CRISPR

期刊名称：GENE （ 影响因子：3.5； 五年影响因子：3.3 ）

ISSN： 0378-1119

年卷期： 2023 年 851 卷

页码：

收录情况： SCI

摘要： The DNA polymerase delta (Pol delta), a heterotetramer of four subunits (Pol delta 4), plays a pivotal role in DNA replication, as well as in DNA damage repair. Pold4, as the smallest subunit of Pol delta, is degraded in response to DNA damage or when entering into S-phase. This leads to the conversion of Pol delta 4 to the trimeric complex Pol delta 3. However, the contribution of Pold4 has not been fully elucidated in mammals. Cdm1, the Pold4 ortholog in Schizosaccharomyces pombe, is dispensable for cell growth and DNA damage repair, and there are no Pold4 orthologs in Saccharomyces cerevisiae. We previously generated a knockout mouse model of Pold3 and revealed its essential role in genome stability. Unexpectedly, we here found that Pold4 knockout mice are viable and fertile. In addition, Pold4 knockout mice do not exhibit any pathologic changes in the lung and spleen, tissues with the most abundant expression of Pold4. Moreover, Pold4 knockout mouse tail tip fibroblasts (TTF) exhibited normal cell growth, cell cycle, DNA replication, DNA damage and DNA repair capacity. These results suggested that Pol delta 3 but not Pol delta 4 may be responsible for these processes in normal cells. Interestingly, 19-month-old wild-type (WT) mice had tumors in the liver, while Pold4 knockout mice did not, and Pold4 knockout mice showed increased longevity. In further, this provided evidence suggested that Pold4 could be a potential novel target for lung carcinoma because its depletion does not affect normal cells but does affect cancer cells.

分类号：

  • 相关文献
作者其他论文 更多>>

微信小程序