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

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: 7.500

Kód RIV

RIV/00216224:90242/23:00133755

Organizační jednotka

CIISB III

UT WoS

000964718900001

EID Scopus

2-s2.0-85147311380

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