J 2023

Direct observation of backtracking by influenza A and B polymerases upon consecutive incorporation of the nucleoside analog T1106

KOUBA, Tomas, Anna DUBANKOVA, Petra DRNCOVA, Elisa DONATI, Pietro VIDOSSICH et. al.

Základní údaje

Originální název

Direct observation of backtracking by influenza A and B polymerases upon consecutive incorporation of the nucleoside analog T1106

Autoři

KOUBA, Tomas, Anna DUBANKOVA, Petra DRNCOVA, Elisa DONATI, Pietro VIDOSSICH, Valentina SPERANZINI, Alex PFLUG, Johanna HUCHTING, Chris MEIER, De Vivo MARCO a Stephen CUSACK (garant)

Vydání

Cell Reports, CAMBRIDGE, Cell Press, 2023, 2211-1247

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10601 Cell biology

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 8.800 v roce 2022

Kód RIV

RIV/00216224:90242/23:00133755

Organizační jednotka

CIISB III

UT WoS

000964718900001

Klíčová slova anglicky

T-705 FAVIPIRAVIR; TRANSCRIPTION; RNA polymerase; REPLICATION; INFECTIONS; CryoEM; pyr-azinecarboxamide base analogs

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 11. 4. 2024 23:16, Mgr. Michal Petr

Anotace

V originále

The antiviral pseudo-base T705 and its de-fluoro analog T1106 mimic adenine or guanine and can be compet-itively incorporated into nascent RNA by viral RNA-dependent RNA polymerases. Although dispersed, single pseudo-base incorporation is mutagenic, consecutive incorporation causes polymerase stalling and chain termination. Using a template encoding single and then consecutive T1106 incorporation four nucleotides later, we obtained a cryogenic electron microscopy structure of stalled influenza A/H7N9 polymerase. This shows that the entire product-template duplex backtracks by 5 nt, bringing the singly incorporated T1106 to the +1 position, where it forms an unexpected T1106:U wobble base pair. Similar structures show that influ-enza B polymerase also backtracks after consecutive T1106 incorporation, regardless of whether prior single incorporation has occurred. These results give insight into the unusual mechanism of chain termination by pyr-azinecarboxamide base analogs. Consecutive incorporation destabilizes the proximal end of the product -template duplex, promoting irreversible backtracking to a more energetically favorable overall configuration.

Návaznosti

90242, velká výzkumná infrastruktura
Název: CIISB III