[PDF][PDF] Combined deficiency of Tet1 and Tet2 causes epigenetic abnormalities but is compatible with postnatal development

MM Dawlaty, A Breiling, T Le, G Raddatz, MI Barrasa… - Developmental cell, 2013 - cell.com
MM Dawlaty, A Breiling, T Le, G Raddatz, MI Barrasa, AW Cheng, Q Gao, BE Powell, Z Li…
Developmental cell, 2013cell.com
Summary Tet enzymes (Tet1/2/3) convert 5-methylcytosine (5mC) to 5-
hydroxymethylcytosine (5hmC) in various embryonic and adult tissues. Mice mutant for
either Tet1 or Tet2 are viable, raising the question of whether these enzymes have
overlapping roles in development. Here we have generated Tet1 and Tet2 double-knockout
(DKO) embryonic stem cells (ESCs) and mice. DKO ESCs remained pluripotent but were
depleted of 5hmC and caused developmental defects in chimeric embryos. While a fraction …
Summary
Tet enzymes (Tet1/2/3) convert 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) in various embryonic and adult tissues. Mice mutant for either Tet1 or Tet2 are viable, raising the question of whether these enzymes have overlapping roles in development. Here we have generated Tet1 and Tet2 double-knockout (DKO) embryonic stem cells (ESCs) and mice. DKO ESCs remained pluripotent but were depleted of 5hmC and caused developmental defects in chimeric embryos. While a fraction of double-mutant embryos exhibited midgestation abnormalities with perinatal lethality, viable and overtly normal Tet1/Tet2-deficient mice were also obtained. DKO mice had reduced 5hmC and increased 5mC levels and abnormal methylation at various imprinted loci. Nevertheless, animals of both sexes were fertile, with females having smaller ovaries and reduced fertility. Our data show that loss of both enzymes is compatible with development but promotes hypermethylation and compromises imprinting. The data also suggest a significant contribution of Tet3 to hydroxylation of 5mC during development.
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