DNA polymerase iota (polι) is a member of the Y-family, polymerases which are key components in translesion synthesis (TLS). As part of the DNA damage response, TLS allows cells to bypass damaged template DNA. Each member of the Y-family is capable of accurately replicating across from certain lesions. All Y-family polymerases are recruited by ubiquitination of the DNA sliding clamp, PCNA, by direct interaction with PCNA and ubiquitin. The mechanism of polymerase choice is not well understood, nor are the interactions between Ub-PCNA and the TLS polymerases. We studied the structure of the complex between the interacting region of polι and Ub-PCNA. Polι appears to be unable to bind all three monomers of homotrimeric Ub-PCNA simultaneously, ...
Y-family DNA polymerases carry out translesion synthesis past damaged DNA. DNA polymerases (pol) η a...
DNA polymerase eta is a Y family polymerase involved in translesion synthesis (TLS). Its action is i...
The variant form of the human syndrome xeroderma pigmentosum (XPV) is caused by a deficiency in DNA ...
It has been two decades since the discovery of the most mutagenic human DNA polymerase, polymerase i...
Y-family DNA polymerase κ (Pol κ) can replicate damaged DNA templates to rescue stalled replication ...
DNA damage blocks the progression of the replication fork. In order to circumvent the damaged bases,...
<p>Translesion synthesis (TLS) is a specialized type of DNA repair for bypassing DNA damage at the s...
DNA polymerase iota (Polι) belongs to the Y-family of DNA polymerases that are involved in DNA damag...
DNA polymerases are known to be responsible for the replication and maintenance of an organism’s gen...
In response to DNA damage, TLS (translesion synthesis) allows replicative bypass of various DNA lesi...
International audienceUbiquitin-binding domains (UBDs) provide specificity to the ubiquitin system, ...
DNA synthesis by classical polymerases can be blocked by many lesions. These blocks are overcome by ...
Summary: There are significant ambiguities regarding how DNA polymerase η is recruited to DNA lesion...
Human DNA polymerase iota (pol iota) is a unique member of Y-family polymerases, which preferentiall...
Most types of DNA damage block replication fork progression during DNA synthesis because replicative...
Y-family DNA polymerases carry out translesion synthesis past damaged DNA. DNA polymerases (pol) η a...
DNA polymerase eta is a Y family polymerase involved in translesion synthesis (TLS). Its action is i...
The variant form of the human syndrome xeroderma pigmentosum (XPV) is caused by a deficiency in DNA ...
It has been two decades since the discovery of the most mutagenic human DNA polymerase, polymerase i...
Y-family DNA polymerase κ (Pol κ) can replicate damaged DNA templates to rescue stalled replication ...
DNA damage blocks the progression of the replication fork. In order to circumvent the damaged bases,...
<p>Translesion synthesis (TLS) is a specialized type of DNA repair for bypassing DNA damage at the s...
DNA polymerase iota (Polι) belongs to the Y-family of DNA polymerases that are involved in DNA damag...
DNA polymerases are known to be responsible for the replication and maintenance of an organism’s gen...
In response to DNA damage, TLS (translesion synthesis) allows replicative bypass of various DNA lesi...
International audienceUbiquitin-binding domains (UBDs) provide specificity to the ubiquitin system, ...
DNA synthesis by classical polymerases can be blocked by many lesions. These blocks are overcome by ...
Summary: There are significant ambiguities regarding how DNA polymerase η is recruited to DNA lesion...
Human DNA polymerase iota (pol iota) is a unique member of Y-family polymerases, which preferentiall...
Most types of DNA damage block replication fork progression during DNA synthesis because replicative...
Y-family DNA polymerases carry out translesion synthesis past damaged DNA. DNA polymerases (pol) η a...
DNA polymerase eta is a Y family polymerase involved in translesion synthesis (TLS). Its action is i...
The variant form of the human syndrome xeroderma pigmentosum (XPV) is caused by a deficiency in DNA ...