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
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
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