PUBLICATION

DNA template strand segregation in developing zebrafish

Authors
Glasauer, S.M.K., Triemer, T., Neef, A.B., Neuhauss, S.C.F., Luedtke, N.W.
ID
ZDB-PUB-211001-12
Date
2021
Source
Cell chemical biology   28(11): 1638-1647.e4 (Journal)
Registered Authors
Neuhauss, Stephan
Keywords
DNA metabolic labeling, azide-alkyne "click" cycloaddition, cell division, developmental biology, eye development, fluorescence microscopy, stem cells
MeSH Terms
  • Animals
  • DNA/metabolism*
  • Zebrafish/growth & development
PubMed
34592171 Full text @ Cell Chem Biol
Abstract
Asymmetric inheritance of sister chromatids has long been predicted to be linked to discordant fates of daughter cells and even hypothesized to minimize accumulation of mutations in stem cells. Here, we use (2'S)-2'-deoxy-2'-fluoro-5-ethynyluridine (F-ara-EdU), bromodeoxyuridine (BrdU), and light sheet microscopy to track embryonic DNA in whole zebrafish. Larval development results in rapid depletion of older DNA template strands from stem cell niches in the retina, brain, and intestine. Prolonged label retention occurs in quiescent progenitors that resume replication in later development. High-resolution microscopy reveals no evidence of asymmetric template strand segregation in >100 daughter cell pairs, making it improbable that asymmetric DNA segregation prevents mutational burden according to the immortal strand hypothesis in developing zebrafish.
Genes / Markers
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping