Coordinating DNA polymerase traffic during high and low fidelity synthesis.
Biochimica et biophysica acta (2010), Volume 1804, Page 1167
Abstract:
With the discovery that organisms possess multiple DNA polymerases (Pols) displaying different fidelities, processivities, and activities came the realization that mechanisms must exist to manage the actions of these diverse enzymes to prevent gratuitous mutations. Although many of the Pols encoded by most organisms are largely accurate, and participate in DNA replication and DNA repair, a sizeable fraction display a reduced fidelity, and act to catalyze potentially error-prone translesion DNA synthesis (TLS) past lesions that persist in the DNA. Striking the proper balance between use of these different enzymes during DNA replication, DNA repair, and TLS is essential for ensuring accurate duplication of the cell's genome. This review highlights mechanisms that organisms utilize to manage the actions of their different Pols. A particular emphasis is placed on discussion of current models for how different Pols switch places with each other at the replication fork during high fidelity replication and potentially error-pone TLS.
Polymerases:
Sce Pol lamba,Sce Pol zeta,Human Pol theta,Human Pol gamma,Sce Rev1,Sce Pol epsilon,Sce Pol eta,Sce Pol delta,Sce pol gamma,Sce Pol alpha,Eco Pol V,Eco Pol IV,Eco Pol III,Eco Pol II,Eco Pol I,Human Pol nu,Human Pol alpha,Human Pol delta,Human Pol epsilon,Human Pol zeta,Human Pol beta,Human Pol lamba,Human Pol mu,Human Pol eta,Human Pol iota,Human Pol kappa,Human REV1
Topics:
Status:
new | topics/pols set | partial results | complete | validated |