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-Structure paper
タイトル | Structural insights into human co-transcriptional capping. |
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ジャーナル・号・ページ | Mol Cell, Vol. 83, Issue 14, Page 2464-22477.e5, Year 2023 |
掲載日 | 2023年7月20日 |
著者 | Gaurika Garg / Christian Dienemann / Lucas Farnung / Juliane Schwarz / Andreas Linden / Henning Urlaub / Patrick Cramer / |
PubMed 要旨 | Co-transcriptional capping of the nascent pre-mRNA 5' end prevents degradation of RNA polymerase (Pol) II transcripts and suppresses the innate immune response. Here, we provide mechanistic insights ...Co-transcriptional capping of the nascent pre-mRNA 5' end prevents degradation of RNA polymerase (Pol) II transcripts and suppresses the innate immune response. Here, we provide mechanistic insights into the three major steps of human co-transcriptional pre-mRNA capping based on six different cryoelectron microscopy (cryo-EM) structures. The human mRNA capping enzyme, RNGTT, first docks to the Pol II stalk to position its triphosphatase domain near the RNA exit site. The capping enzyme then moves onto the Pol II surface, and its guanylyltransferase receives the pre-mRNA 5'-diphosphate end. Addition of a GMP moiety can occur when the RNA is ∼22 nt long, sufficient to reach the active site of the guanylyltransferase. For subsequent cap(1) methylation, the methyltransferase CMTR1 binds the Pol II stalk and can receive RNA after it is grown to ∼29 nt in length. The observed rearrangements of capping factors on the Pol II surface may be triggered by the completion of catalytic reaction steps and are accommodated by domain movements in the elongation factor DRB sensitivity-inducing factor (DSIF). |
リンク | Mol Cell / PubMed:37369200 |
手法 | EM (単粒子) |
解像度 | 3.2 - 4.0 Å |
構造データ | EMDB-17403, PDB-8p4a: EMDB-17404, PDB-8p4b: EMDB-17405, PDB-8p4c: EMDB-17406, PDB-8p4d: EMDB-17407, PDB-8p4e: EMDB-17408, PDB-8p4f: |
化合物 | ChemComp-MG: ChemComp-ZN: ChemComp-MGT: ChemComp-SAM: |
由来 |
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キーワード | TRANSCRIPTION / rna polymerase II / capping |