Architecture of Y-Family DNA Polymerases Relevant to Translesion DNA Synthesis as Revealed in Structural and Molecular Modeling Studies. (9th August 2010)

• Record Type: Journal Article
• Authors: Chandani, Sushil; Jacobs, Christopher; Loechler, Edward L.
• Other Names: Basu Ashis Academic Editor.
• Is Part Of: Journal of nucleic acids. Volume 2010(2010)
• Publication Date: 2010-08-09
• Subjects: Nucleic acids -- Periodicals; 572.805
• DOI: 10.4061/2010/784081
• Languages: English
• ISSNs: 2090-0201

Abstract

Abstract : DNA adducts, which block replicative DNA polymerases (DNAPs), are often bypassed by lesion-bypass DNAPs, which are mostly in the Y-Family. Y-Family DNAPs can do non-mutagenic or mutagenic dNTP insertion, and understanding this difference is important, because mutations transform normal into tumorigenic cells. Y-Family DNAP architecture that dictates mechanism, as revealed in structural and modeling studies, is considered. Steps from adduct blockage of replicative DNAPs, to bypass by a lesion-bypass DNAP, to resumption of synthesis by a replicative DNAP are described. Catalytic steps and protein conformational changes are considered. One adduct is analyzed in greater detail: the major benzo[a]pyrene adduct( B [ a ] P-N 2 -dG ), which is bypassed non-mutagenically (dCTP insertion) by Y-family DNAPs in the IV/κ -class and mutagenically (dATP insertion) by V/η -class Y-Family DNAPs. Important architectural differences between IV/κ -class versus V/η -class DNAPs are discussed, including insights gained by analyzing ~400 sequences each for bacterial DNAPs IV and V, along with sequences from eukaryotic DNAPs kappa, eta and iota. The little finger domains of Y-Family DNAPs do not show sequence conservation; however, their structures are remarkably similar due to the presence of a core of hydrophobic amino acids, whose exact identity is less important than the hydrophobic amino acid spacing.