Beijing Key Laboratory of DNA Damage Responses and College of Life Sciences, Capital Normal University, Beijing, 100048, China.
Department of Microbiology and Immunology, University of Saskatchewan, Saskatoon, S7N 5E5, Canada.
Apoptosis. 2018 Jan;23(1):16-26. doi: 10.1007/s10495-017-1433-8.
Ubiquitination of proliferating cell nuclear antigen (PCNA) plays an important role in DNA damage response. Ectopic expression of PCNA fused at either terminus with ubiquitin (Ub) lacking two C-terminal glycine residues induces translesion DNA synthesis which resembles synthesis mediated by PCNA monoubiquitination. PCNA fused with Ub containing the C-terminal Gly residues at the C-terminus can be further polyubiquitinated in a Gly-dependent manner, which inhibits cell proliferation and induces ATR-dependent replication checkpoint. In this study, we surprisingly found that PCNA fused to a head-to-tail linear Ub chain induces apoptosis in a Ub chain length-dependent manner. Further investigation revealed that the apoptotic effect is actually induced by the linear Ub chain independently from PCNA, as the Ub chain fused to GFP or an epitope tag still efficiently induces apoptosis. It is revealed that the artificial linear Ub chain differs from endogenously encoded linear Ub chains in that its Ubs contain a Ub-G76S substitution, making the Ub chain resistant to cleavage by deubiquitination enzymes. We demonstrated in this study that ectopic expression of the artificial Ub chain alone in cultured human cancer cells is sufficient to inhibit tumor growth in a xenograft mouse model, making the linear Ub chain a putative anti-cancer agent.
泛素化增殖细胞核抗原(PCNA)在 DNA 损伤反应中起着重要作用。PCNA 与缺乏两个 C 末端甘氨酸残基的泛素(Ub)在两端融合的异位表达诱导跨损伤 DNA 合成,类似于由 PCNA 单泛素化介导的合成。与在 C 末端具有 C 末端甘氨酸残基的 Ub 融合的 PCNA 可以以 Gly 依赖性方式进一步多泛素化,这抑制细胞增殖并诱导 ATR 依赖性复制检查点。在这项研究中,我们惊讶地发现,与从头至尾的线性 Ub 链融合的 PCNA 以 Ub 链长度依赖性方式诱导细胞凋亡。进一步的研究表明,凋亡效应实际上是由线性 Ub 链独立于 PCNA 诱导的,因为融合到 GFP 或表位标签的 Ub 链仍然有效地诱导凋亡。结果表明,人工线性 Ub 链与内源性编码的线性 Ub 链不同,因为其 Ubs 含有 Ub-G76S 取代,使 Ub 链不易被去泛素化酶切割。我们在这项研究中证明,在培养的人类癌细胞中单独表达外源线性 Ub 链足以抑制异种移植小鼠模型中的肿瘤生长,使线性 Ub 链成为一种潜在的抗癌药物。