Related Experiment Video
Updated: Jan 23, 2026

DNA Stable-Isotope Probing DNA-SIP
Published on: August 2, 2010
Protection of abasic sites during DNA replication by a stable thiazolidine protein-DNA cross-link
Petria S Thompson1, Katherine M Amidon2, Kareem N Mohni1
1Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, USA.
Abstract:
Abasic (AP) sites are one of the most common DNA lesions that block replicative polymerases. 5-hydroxymethylcytosine binding, embryonic stem cell-specific protein (HMCES) recognizes and processes these lesions in the context of single-stranded DNA (ssDNA). A HMCES DNA-protein cross-link (DPC) intermediate is thought to shield the AP site from endonucleases and error-prone polymerases. The highly evolutionarily conserved SOS-response associated peptidase (SRAP) domain of HMCES and its Escherichia coli ortholog YedK mediate lesion recognition. Here we uncover the basis of AP site protection by SRAP domains from a crystal structure of the YedK DPC. YedK forms a stable thiazolidine linkage between a ring-opened AP site and the α-amino and sulfhydryl substituents of its amino-terminal cysteine residue. The thiazolidine linkage explains the remarkable stability of the HMCES DPC, its resistance to strand cleavage and the proteolysis requirement for resolution. Furthermore, its structure reveals that HMCES has specificity for AP sites in ssDNA at junctions found when replicative polymerases encounter the AP lesion.
Insights
The study reveals how a protein called HMCES protects DNA from damage by forming a stable link with abasic (AP) sites. This DNA-protein cross-link prevents harmful enzymes from accessing the lesion, ensuring DNA repair.
Area of Science:
- Molecular Biology
- Structural Biology
- DNA Repair Mechanisms
Background:
- Abasic (AP) sites are frequent DNA lesions that impede DNA replication.
- 5-hydroxymethylcytosine binding, embryonic stem cell-specific protein (HMCES) processes AP sites in single-stranded DNA (ssDNA).
- HMCES forms a DNA-protein cross-link (DPC) intermediate to shield AP sites.
Purpose of the Study:
- To elucidate the structural basis of AP site protection by SRAP domains.
- To understand the mechanism of DNA-protein cross-link formation and stability.
Main Methods:
- X-ray crystallography of the YedK DPC complex.
- Structural analysis of the YedK protein-DNA interaction.
Main Results:
- The crystal structure of the YedK DPC reveals a stable thiazolidine linkage.
- This linkage forms between a ring-opened AP site and YedK's N-terminal cysteine.
- The thiazolidine bond confers stability to the DPC, resisting strand cleavage.
Conclusions:
- The SRAP domain's thiazolidine linkage explains the stability of HMCES DPCs.
- HMCES DPCs require proteolysis for resolution.
- HMCES specifically recognizes AP sites in ssDNA at replication fork junctions.
More Related Videos
09:31Amplification, Next-generation Sequencing, and Genomic DNA Mapping of Retroviral Integration Sites
Published on: March 22, 2016
08:53Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
Published on: May 2, 2025
Related Concept Videos
DNA Replication
Replication in Prokaryotes
DNA replication...
The DNA Replication Fork
The DNA Replication Fork
Translesion DNA Polymerases
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
From DNA to Protein
DNA Helicases