Summary information and primary citation
- PDB-id
-
3t5l;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- DNA-transferase
- Method
- X-ray (2.9 Å)
- Summary
- Ternary complex of hne adduct modified DNA (5'-cxg-3'
vs 14-mer) with dpo4 and incoming ddgt
- Reference
-
Banerjee S, Christov PP, Kozekova A, Rizzo CJ, Egli M,
Stone MP (2012): "Replication
bypass of the trans-4-Hydroxynonenal-derived
(6S,8R,11S)-1,N(2)-deoxyguanosine DNA adduct by the
sulfolobus solfataricus DNA polymerase IV."
Chem.Res.Toxicol., 25, 422-435.
doi: 10.1021/tx200460j.
- Abstract
- trans-4-Hydroxynonenal (HNE) is the major peroxidation
product of ω-6 polyunsaturated fatty acids in vivo. Michael
addition of the N(2)-amino group of dGuo to HNE followed by
ring closure of N1 onto the aldehyde results in four
diastereomeric 1,N(2)-dGuo (1,N(2)-HNE-dGuo) adducts. The
(6S,8R,11S)-HNE-1,N(2)-dGuo adduct was incorporated into
the 18-mer templates 5'-d(TCATXGAATCCTTCCCCC)-3' and
d(TCACXGAATCCTTCCCCC)-3', where X =
(6S,8R,11S)-HNE-1,N(2)-dGuo adduct. These differed in the
identity of the template 5'-neighbor base, which was either
Thy or Cyt, respectively. Each of these templates was
annealed with either a 13-mer primer 5'-d(GGGGGAAGGATTC)-3'
or a 14-mer primer 5'-d(GGGGGAAGGATTCC)-3'. The addition of
dNTPs to the 13-mer primer allowed analysis of dNTP
insertion opposite to the (6S,8R,11S)-HNE-1,N(2)-dGuo
adduct, whereas the 14-mer primer allowed analysis of dNTP
extension past a primed (6S,8R,11S)-HNE-1,N(2)-dGuo:dCyd
pair. The Sulfolobus solfataricus P2 DNA polymerase IV
(Dpo4) belongs to the Y-family of error-prone polymerases.
Replication bypass studies in vitro reveal that this
polymerase inserted dNTPs opposite the
(6S,8R,11S)-HNE-1,N(2)-dGuo adduct in a sequence-specific
manner. If the template 5'-neighbor base was dCyt, the
polymerase inserted primarily dGTP, whereas if the template
5'-neighbor base was dThy, the polymerase inserted
primarily dATP. The latter event would predict low levels
of Gua → Thy mutations during replication bypass when the
template 5'-neighbor base is dThy. When presented with a
primed (6S,8R,11S)-HNE-1,N(2)-dGuo:dCyd pair, the
polymerase conducted full-length primer extension.
Structures for ternary (Dpo4-DNA-dNTP) complexes with all
four template-primers were obtained. For the 18-mer:13-mer
template-primers in which the polymerase was confronted
with the (6S,8R,11S)-HNE-1,N(2)-dGuo adduct, the
(6S,8R,11S)-1,N(2)-dGuo lesion remained in the ring-closed
conformation at the active site. The incoming dNTP, either
dGTP or dATP, was positioned with Watson-Crick pairing
opposite the template 5'-neighbor base, dCyt or dThy,
respectively. In contrast, for the 18-mer:14-mer
template-primers with a primed
(6S,8R,11S)-HNE-1,N(2)-dGuo:dCyd pair, ring opening of the
adduct to the corresponding N(2)-dGuo aldehyde species
occurred. This allowed Watson-Crick base pairing at the
(6S,8R,11S)-HNE-1,N(2)-dGuo:dCyd pair.