Haracska L, Johnson R E, Unk I, Phillips B, Hurwitz J, Prakash L, Prakash S
Sealy Center for Molecular Science, University of Texas Medical Branch, Galveston, Texas 77555-1061, USA.
Mol Cell Biol. 2001 Nov;21(21):7199-206. doi: 10.1128/MCB.21.21.7199-7206.2001.
Human DNA polymerase eta (hPoleta) functions in the error-free replication of UV-damaged DNA, and mutations in hPoleta cause cancer-prone syndrome, the variant form of xeroderma pigmentosum. However, in spite of its key role in promoting replication through a variety of distorting DNA lesions, the manner by which hPoleta is targeted to the replication machinery stalled at a lesion site remains unknown. Here, we provide evidence for the physical interaction of hPoleta with proliferating cell nuclear antigen (PCNA) and show that mutations in the PCNA binding motif of hPoleta inactivate this interaction. PCNA, together with replication factor C and replication protein A, stimulates the DNA synthetic activity of hPoleta, and steady-state kinetic studies indicate that this stimulation accrues from an increase in the efficiency of nucleotide insertion resulting from a reduction in the apparent K(m) for the incoming nucleotide.
人类DNA聚合酶η(hPoleta)在紫外线损伤DNA的无差错复制中发挥作用,hPoleta的突变会导致易患癌症的综合征——着色性干皮病的变异型。然而,尽管hPoleta在促进通过各种扭曲DNA损伤的复制中起关键作用,但hPoleta被靶向到停滞在损伤位点的复制机器的方式仍不清楚。在这里,我们提供了hPoleta与增殖细胞核抗原(PCNA)发生物理相互作用的证据,并表明hPoleta的PCNA结合基序中的突变会使这种相互作用失活。PCNA与复制因子C和复制蛋白A一起刺激hPoleta的DNA合成活性,稳态动力学研究表明,这种刺激源于由于进入核苷酸的表观K(m)降低导致的核苷酸插入效率的提高。