Mesoscale DNA Features Impact APOBEC3A and APOBEC3B Deaminase Activity and Shape Tumor Mutational Landscapes

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.