Cell Reports
Volume 13, Issue 8, 24 November 2015, Pages 1692-1704
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Article
Combined Loss of Tet1 and Tet2 Promotes B Cell, but Not Myeloid Malignancies, in Mice

https://doi.org/10.1016/j.celrep.2015.10.037Get rights and content
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Highlights

  • TET1 and TET2 are often concomitantly downregulated in acute B-lymphocytic leukemia

  • Tet1 is required for Tet2-deletion-mediated HSC dysregulation and myeloid malignancy

  • Deletion of both Tet1 and Tet2 in mice leads to lethal B cell malignancies

  • Tet2−/− and DKO HSC/HPCs display distinct DNA 5hmC/5mC signatures

Summary

TET1/2/3 are methylcytosine dioxygenases that regulate cytosine hydroxymethylation. Tet1/2 are abundantly expressed in HSC/HPCs and are implicated in hematological malignancies. Tet2 deletion in mice causes myeloid malignancies, while Tet1-null mice develop B cell lymphoma after an extended period of latency. Interestingly, TET1/2 are often concomitantly downregulated in acute B-lymphocytic leukemia. Here, we investigated the overlapping and non-redundant functions of Tet1/2 using Tet1/2 double-knockout (DKO) mice. DKO and Tet2−/− HSC/HPCs show overlapping and unique 5hmC and 5mC profiles. DKO mice exhibit strikingly decreased incidence and delayed onset of myeloid malignancies in comparison to Tet2−/− mice and in contrast develop lethal B cell malignancies. Transcriptome analysis of DKO tumors reveals expression changes in many genes dysregulated in human B cell malignancies, including LMO2, BCL6, and MYC. These results highlight the critical roles of TET1/2 individually and together in the pathogenesis of hematological malignancies.

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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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Co-first author