The replicative bypass of base damage in DNA (translesion DNA synthesis [TLS]) is a ubiquitous mechanism for relieving arrested DNA replication. The process requires multiple polymerase switching events during which the high-fidelity DNA polymerase in the replication machinery arrested at the primer terminus is replaced by one or more polymerases that are specialized for TLS. When replicative bypass is fully completed, the primer terminus is once again occupied by high-fidelity polymerases in the replicative machinery. This review addresses recent advances in our understanding of DNA polymerase switching during TLS in bacteria such as E. coli and in lower and higher eukaryotes
Proofreading by replicative DNA polymerases is a fundamental mechanism ensuring DNA replication fide...
Translesion synthesis (TLS) DNA polymerases allow the bypass of unrepaired lesions during DNA replic...
Translesion synthesis (TLS) DNA polymerases allow the bypass of unrepaired lesions during DNA replic...
DNA replication is constantly challenged by DNA lesions, noncanonical DNA structures and difficult-t...
DNA replication is constantly challenged by DNA lesions, noncanonical DNA structures and difficult-t...
Translesion synthesis (TLS) by Y-family DNA polymerases alleviates replication stalling at DNA damag...
Translesion synthesis (TLS) alleviates replication stalling at DNA lesions. Bypass of lesions by spe...
In many bacterial species, DNA damage triggers the SOS response; a pathway that regulates the produc...
Replicative DNA polymerases are blocked at DNA lesions. Synthesis past DNA damage requires the repla...
Replicative DNA polymerases are blocked at DNA lesions. Synthesis past DNA damage requires the repla...
DNA damage is generated continually inside cells. In order to be able to replicate past damaged base...
Most types of DNA damage block the passage of the replication machinery. In order to bypass these bl...
DNA damage blocks the progression of the replication fork. In order to circumvent the damaged bases,...
AbstractMost types of DNA damage block the passage of the replication machinery. In order to bypass ...
SummaryE. coli DNA Pol II and eukaryotic Rev3 are B-family polymerases that can extend primers past ...
Proofreading by replicative DNA polymerases is a fundamental mechanism ensuring DNA replication fide...
Translesion synthesis (TLS) DNA polymerases allow the bypass of unrepaired lesions during DNA replic...
Translesion synthesis (TLS) DNA polymerases allow the bypass of unrepaired lesions during DNA replic...
DNA replication is constantly challenged by DNA lesions, noncanonical DNA structures and difficult-t...
DNA replication is constantly challenged by DNA lesions, noncanonical DNA structures and difficult-t...
Translesion synthesis (TLS) by Y-family DNA polymerases alleviates replication stalling at DNA damag...
Translesion synthesis (TLS) alleviates replication stalling at DNA lesions. Bypass of lesions by spe...
In many bacterial species, DNA damage triggers the SOS response; a pathway that regulates the produc...
Replicative DNA polymerases are blocked at DNA lesions. Synthesis past DNA damage requires the repla...
Replicative DNA polymerases are blocked at DNA lesions. Synthesis past DNA damage requires the repla...
DNA damage is generated continually inside cells. In order to be able to replicate past damaged base...
Most types of DNA damage block the passage of the replication machinery. In order to bypass these bl...
DNA damage blocks the progression of the replication fork. In order to circumvent the damaged bases,...
AbstractMost types of DNA damage block the passage of the replication machinery. In order to bypass ...
SummaryE. coli DNA Pol II and eukaryotic Rev3 are B-family polymerases that can extend primers past ...
Proofreading by replicative DNA polymerases is a fundamental mechanism ensuring DNA replication fide...
Translesion synthesis (TLS) DNA polymerases allow the bypass of unrepaired lesions during DNA replic...
Translesion synthesis (TLS) DNA polymerases allow the bypass of unrepaired lesions during DNA replic...