+検索条件
-Structure paper
タイトル | Structures of the human leading strand Polε-PCNA holoenzyme. |
---|---|
ジャーナル・号・ページ | Nat Commun, Vol. 15, Issue 1, Page 7847, Year 2024 |
掲載日 | 2024年9月8日 |
著者 | Qing He / Feng Wang / Nina Y Yao / Michael E O'Donnell / Huilin Li / |
PubMed 要旨 | In eukaryotes, the leading strand DNA is synthesized by Polε and the lagging strand by Polδ. These replicative polymerases have higher processivity when paired with the DNA clamp PCNA. While the ...In eukaryotes, the leading strand DNA is synthesized by Polε and the lagging strand by Polδ. These replicative polymerases have higher processivity when paired with the DNA clamp PCNA. While the structure of the yeast Polε catalytic domain has been determined, how Polε interacts with PCNA is unknown in any eukaryote, human or yeast. Here we report two cryo-EM structures of human Polε-PCNA-DNA complex, one in an incoming nucleotide bound state and the other in a nucleotide exchange state. The structures reveal an unexpected three-point interface between the Polε catalytic domain and PCNA, with the conserved PIP (PCNA interacting peptide)-motif, the unique P-domain, and the thumb domain each interacting with a different protomer of the PCNA trimer. We propose that the multi-point interface prevents other PIP-containing factors from recruiting to PCNA while PCNA functions with Polε. Comparison of the two states reveals that the finger domain pivots around the [4Fe-4S] cluster-containing tip of the P-domain to regulate nucleotide exchange and incoming nucleotide binding. |
リンク | Nat Commun / PubMed:39245668 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.95 - 5.01 Å |
構造データ | EMDB-44357, PDB-9b8s: EMDB-44358, PDB-9b8t: |
化合物 | ChemComp-SF4: ChemComp-TTP: ChemComp-MG: |
由来 |
|
キーワード | DNA Binding Protein/DNA / DNA polymerase / DNA / DNA Binding Protein-DNA complex |