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Mesoscale DNA Features Impact APOBEC3A and APOBEC3B Deaminase Activity and Shape Tumor Mutational Landscapes
Abstract:
Antiviral DNA cytosine deaminases APOBEC3A and APOBEC3B are major sources of mutations in cancer by catalyzing cytosine-to-uracil deamination. APOBEC3A preferentially targets singlestranded DNAs, with a noted affinity for DNA regions that adopt stem-loop secondary structures. However, the detailed substrate preferences of APOBEC3A and APOBEC3B have been fully established, and the specific influence of the DNA sequence on APOBEC3A APOBEC3B deaminase activity remains to be investigated. Here, we find that APOBEC3B selectively targets DNA stem-loop structures, and they are distinct from those subjected deamination by APOBEC3A. We develop Oligo-seq, a novel in vitro sequencing-based to identify specific sequence contexts promoting APOBEC3A and APOBEC3B activity. Through this approach, we demonstrate that APOBEC3A an APOBEC3B deaminase activity is strongly regulated by specific sequences surrounding the targeted cytosine. Moreover, we identify structural features of APOBEC3B and APOBEC3A responsible for their substrate preferences. Importantly, we determine that APOBEC3B-induced mutations in hairpin-forming sequences within tumor genomes differ from the DNA stem-loop sequences mutated by APOBEC3A. Together, our study provides evidence that APOBEC3A and APOBEC3B can generate mutation landscapes in cancer genomes, driven by their unique substrate selectivity.
Insights
The DNA-editing enzymes APOBEC3A (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A) and APOBEC3B (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3B) generate distinct cancer mutation patterns. Their unique sequence preferences dictate where these mutations occur in DNA.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Antiviral DNA cytosine deaminases, APOBEC3A and APOBEC3B, are significant contributors to cancer mutations via cytosine-to-uracil deamination.
- APOBEC3A shows a preference for single-stranded DNA, particularly in stem-loop structures, but detailed substrate specificities remain unclear.
Approach:
- Developed Oligo-seq, a novel in vitro sequencing-based method to identify sequence contexts influencing APOBEC3A and APOBEC3B activity.
- Investigated the distinct substrate preferences and sequence specificities of APOBEC3A and APOBEC3B.
Key Points:
- APOBEC3B selectively targets DNA stem-loop structures, distinct from those targeted by APOBEC3A.
- Both enzymes' deaminase activity is strongly regulated by specific DNA sequences surrounding the target cytosine.
- Identified structural features responsible for the substrate preferences of APOBEC3A and APOBEC3B.
Conclusions:
- APOBEC3A and APOBEC3B exhibit unique substrate selectivity, leading to distinct mutation patterns in cancer genomes.
- APOBEC3B-induced mutations in hairpin-forming DNA sequences differ from those induced by APOBEC3A.
- These findings elucidate how APOBEC3A and APOBEC3B shape cancer mutation landscapes through their specific DNA targeting mechanisms.

