催化亚单位
DNA修复
细胞生物学
蛋白质亚单位
同源重组
DNA
非同源性末端接合
生物
DNA修复蛋白XRCC4
分子生物学
V(D)J复合
化学
遗传学
基因
重组
核苷酸切除修复
作者
Ye-Rim Lee,Gi-Sue Kang,Taerim Oh,Hye-Ju Jo,Hye-Joon Park,G‐One Ahn
出处
期刊:Molecules and Cells
[Korean Society for Molecular and Cellular Biology]
日期:2023-02-09
卷期号:46 (4): 200-205
被引量:9
标识
DOI:10.14348/molcells.2023.2164
摘要
DNA-dependent protein kinase catalytic subunit (DNA-PKcs), a member of the phosphatidylinositol 3-kinase related kinase family is a well-known player in repairing DNA double strand break through non-homologous end joining pathway. This mechanism has allowed us to understand its critical role in T and B cell development through V(D)J recombination and class switch recombination, respectively. We have also learned that the defects in these mechanisms lead to severely combined immunodeficiency (SCID). Here we highlight some of the latest evidence where DNA-PKcs has been shown to localize not only in the nucleus but also in the cytoplasm, phosphorylating various proteins involved in cellular metabolism and cytokine production. While it is an exciting time to unveil novel functions of DNA-PKcs, one should carefully choose experimental models to study DNA-PKcs as the experimental evidence has been shown to differ between cells of defective DNA-PKcs and those of
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