Laboratory of Mutagenesis and DNA Damage Tolerance, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Laboratory of Molecular and Cellular Neurobiology, International Institute of Molecular and Cell Biology, ul. Ks. Trojdena 4, 02-109 Warsaw, Poland.
Biochim Biophys Acta Mol Cell Res. 2024 Jun;1871(5):119743. doi: 10.1016/j.bbamcr.2024.119743. Epub 2024 May 3.
Human DNA polymerase ι (Polι) belongs to the Y-family of specialized DNA polymerases engaged in the DNA damage tolerance pathway of translesion DNA synthesis that is crucial to the maintenance of genome integrity. The extreme infidelity of Polι and the fact that both its up- and down-regulation correlate with various cancers indicate that Polι expression and access to the replication fork should be strictly controlled. Here, we identify RNF2, an E3 ubiquitin ligase, as a new interacting partner of Polι that is responsible for Polι stabilization in vivo. Interestingly, while we report that RNF2 does not directly ubiquitinate Polι, inhibition of the E3 ubiquitin ligase activity of RNF2 affects the cellular level of Polι thereby protecting it from destabilization. Additionally, we indicate that this mechanism is more general, as DNA polymerase η, another Y-family polymerase and the closest paralogue of Polι, share similar features.
人类 DNA 聚合酶 ι(Polι)属于 Y 家族的专门 DNA 聚合酶,参与跨损伤 DNA 合成的 DNA 损伤容忍途径,这对维持基因组完整性至关重要。Polι 的极端保真度以及其上调和下调都与各种癌症相关这一事实表明,Polι 的表达和对复制叉的访问应该受到严格控制。在这里,我们确定 RNF2(一种 E3 泛素连接酶)是 Polι 的一个新的相互作用伙伴,它负责 Polι 在体内的稳定。有趣的是,虽然我们报告 RNF2 并不直接泛素化 Polι,但抑制 RNF2 的 E3 泛素连接酶活性会影响细胞内 Polι 的水平,从而防止其不稳定。此外,我们还表明,这种机制更为普遍,因为另一种 Y 家族聚合酶 DNA 聚合酶 η(Polι 的最接近的旁系同源物)也具有类似的特征。