tetano
Editor, Senior Moderator
Nature
. 2026 Mar 4.
doi: 10.1038/s41586-026-10189-0. Online ahead of print.
Mechanism of co-transcriptional cap snatching by influenza polymerase
Alexander Helmut Rotsch[SUP] #[/SUP][SUP] 1 [/SUP], Delong Li[SUP] #[/SUP][SUP] 1 2 [/SUP], Maud Dupont[SUP] #[/SUP][SUP] 3 [/SUP], Tim Krischuns[SUP] 3 [/SUP], Ute Neef[SUP] 1 [/SUP], Christiane Oberthür[SUP] 1 [/SUP], Alice Stelfox[SUP] 4 [/SUP], Maria Lukarska[SUP] 4 5 [/SUP], Isaac Fianu[SUP] 1 6 [/SUP], Michael Lidschreiber[SUP] 1 [/SUP], Nadia Naffakh[SUP] 7 [/SUP], Christian Dienemann[SUP] 8 [/SUP], Stephen Cusack[SUP] 9 [/SUP], Patrick Cramer[SUP] 10 [/SUP]
Affiliations
Influenza virus mRNAs are stable and competent for nuclear export and translation because they receive a 5' cap(1) structure in a process called cap snatching[SUP]1[/SUP]. During cap snatching, the viral RNA-dependent RNA polymerase (FluPol) binds to host RNA polymerase II (Pol II) and the emerging transcript[SUP]2,3[/SUP]. The FluPol endonuclease then cleaves a capped RNA fragment that subsequently acts as a primer for the transcription of viral genes[SUP]4,5[/SUP]. Here we present the cryogenic electron microscopy structure of FluPol bound to a transcribing Pol II in complex with the elongation factor DSIF in the pre-cleavage state. The structure shows that FluPol directly interacts with both Pol II and DSIF, positioning the FluPol endonuclease domain near the RNA exit channel of Pol II. These interactions are important for the endonuclease activity of FluPol and FluPol activity in cells. A second structure, trapped after cap snatching, shows that the cleaved capped RNA rearranges within FluPol, directing the capped RNA 3' end toward the FluPol polymerase active site for viral transcription initiation. Together, our results provide the molecular mechanisms of co-transcriptional cap snatching by FluPol.
. 2026 Mar 4.
doi: 10.1038/s41586-026-10189-0. Online ahead of print.
Mechanism of co-transcriptional cap snatching by influenza polymerase
Alexander Helmut Rotsch[SUP] #[/SUP][SUP] 1 [/SUP], Delong Li[SUP] #[/SUP][SUP] 1 2 [/SUP], Maud Dupont[SUP] #[/SUP][SUP] 3 [/SUP], Tim Krischuns[SUP] 3 [/SUP], Ute Neef[SUP] 1 [/SUP], Christiane Oberthür[SUP] 1 [/SUP], Alice Stelfox[SUP] 4 [/SUP], Maria Lukarska[SUP] 4 5 [/SUP], Isaac Fianu[SUP] 1 6 [/SUP], Michael Lidschreiber[SUP] 1 [/SUP], Nadia Naffakh[SUP] 7 [/SUP], Christian Dienemann[SUP] 8 [/SUP], Stephen Cusack[SUP] 9 [/SUP], Patrick Cramer[SUP] 10 [/SUP]
Affiliations
- PMID: 41781612
- DOI: 10.1038/s41586-026-10189-0
Influenza virus mRNAs are stable and competent for nuclear export and translation because they receive a 5' cap(1) structure in a process called cap snatching[SUP]1[/SUP]. During cap snatching, the viral RNA-dependent RNA polymerase (FluPol) binds to host RNA polymerase II (Pol II) and the emerging transcript[SUP]2,3[/SUP]. The FluPol endonuclease then cleaves a capped RNA fragment that subsequently acts as a primer for the transcription of viral genes[SUP]4,5[/SUP]. Here we present the cryogenic electron microscopy structure of FluPol bound to a transcribing Pol II in complex with the elongation factor DSIF in the pre-cleavage state. The structure shows that FluPol directly interacts with both Pol II and DSIF, positioning the FluPol endonuclease domain near the RNA exit channel of Pol II. These interactions are important for the endonuclease activity of FluPol and FluPol activity in cells. A second structure, trapped after cap snatching, shows that the cleaved capped RNA rearranges within FluPol, directing the capped RNA 3' end toward the FluPol polymerase active site for viral transcription initiation. Together, our results provide the molecular mechanisms of co-transcriptional cap snatching by FluPol.