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7Q73

Structure of Pla1 apo

7Q73 の概要
エントリーDOI10.2210/pdb7q73/pdb
分子名称Poly(A) polymerase pla1, GLYCEROL (3 entities in total)
機能のキーワードpolya polymerase, transferase
由来する生物種Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast)
タンパク質・核酸の鎖数1
化学式量合計65472.95
構造登録者
Soni, K.,Wild, K.,Sinning, I. (登録日: 2021-11-09, 公開日: 2022-12-07, 最終更新日: 2024-02-07)
主引用文献Soni, K.,Sivadas, A.,Horvath, A.,Dobrev, N.,Hayashi, R.,Kiss, L.,Simon, B.,Wild, K.,Sinning, I.,Fischer, T.
Mechanistic insights into RNA surveillance by the canonical poly(A) polymerase Pla1 of the MTREC complex.
Nat Commun, 14:772-772, 2023
Cited by
PubMed Abstract: The S. pombe orthologue of the human PAXT connection, Mtl1-Red1 Core (MTREC), is an eleven-subunit complex that targets cryptic unstable transcripts (CUTs) to the nuclear RNA exosome for degradation. It encompasses the canonical poly(A) polymerase Pla1, responsible for polyadenylation of nascent RNA transcripts as part of the cleavage and polyadenylation factor (CPF/CPSF). In this study we identify and characterise the interaction between Pla1 and the MTREC complex core component Red1 and analyse the functional relevance of this interaction in vivo. Our crystal structure of the Pla1-Red1 complex shows that a 58-residue fragment in Red1 binds to the RNA recognition motif domain of Pla1 and tethers it to the MTREC complex. Structure-based Pla1-Red1 interaction mutations show that Pla1, as part of MTREC complex, hyper-adenylates CUTs for their efficient degradation. Interestingly, the Red1-Pla1 interaction is also required for the efficient assembly of the fission yeast facultative heterochromatic islands. Together, our data suggest a complex interplay between the RNA surveillance and 3'-end processing machineries.
PubMed: 36774373
DOI: 10.1038/s41467-023-36402-6
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 7q73
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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