Fluorescent dATP for DNA Synthesis In Vivo

ACS Chem Biol. 2020 Nov 20;15(11):2996-3003. doi: 10.1021/acschembio.0c00654. Epub 2020 Oct 27.

Abstract

Fluorescent nucleoside triphosphates are powerful probes of DNA synthesis, but their potential use in living animals has been previously underexplored. Here, we report the synthesis and characterization of 7-deaza-(1,2,3-triazole)-2'-deoxyadenosine-5'-triphosphate (dATP) derivatives of tetramethyl rhodamine ("TAMRA-dATP"), cyanine ("Cy3-dATP"), and boron-dipyrromethene ("BODIPY-dATP"). Upon microinjection into live zebrafish embryos, all three compounds were incorporated into the DNA of dividing cells; however, their impact on embryonic toxicity was highly variable, depending on the exact structure of the dye. TAMRA-EdATP exhibited superior characteristics in terms of its high brightness, low toxicity, and rapid incorporation and depletion kinetics in both a vertebrate (zebrafish) and a nematode (Caenorhabditis elegans). TAMRA-EdATP allows for unprecedented, real-time visualization of DNA replication and chromosome segregation in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Boron Compounds / chemical synthesis
  • Boron Compounds / chemistry
  • Caenorhabditis elegans / ultrastructure
  • Carbocyanines / chemical synthesis
  • Carbocyanines / chemistry
  • DNA / analysis*
  • DNA Replication*
  • Deoxyadenine Nucleotides / chemical synthesis
  • Deoxyadenine Nucleotides / chemistry*
  • Fluorescent Dyes / chemical synthesis
  • Fluorescent Dyes / chemistry*
  • Optical Imaging / methods
  • Rhodamines / chemical synthesis
  • Rhodamines / chemistry
  • Zebrafish / embryology

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Carbocyanines
  • Deoxyadenine Nucleotides
  • Fluorescent Dyes
  • Rhodamines
  • cyanine dye 3
  • DNA
  • 2'-deoxyadenosine triphosphate