TY - JOUR T1 - Variants of <em>DNMT3A</em> cause transcript-specific DNA methylation patterns and affect hematopoiesis JF - Life Science Alliance JO - Life Sci. Alliance DO - 10.26508/lsa.201800153 VL - 1 IS - 6 SP - e201800153 AU - Tanja Božić AU - Joana Frobel AU - Annamarija Raic AU - Fabio Ticconi AU - Chao-Chung Kuo AU - Stefanie Heilmann-Heimbach AU - Tamme W Goecke AU - Martin Zenke AU - Edgar Jost AU - Ivan G Costa AU - Wolfgang Wagner Y1 - 2018/12/01 UR - https://www.life-science-alliance.org/content/1/6/e201800153.abstract N2 - De novo DNA methyltransferase 3A (DNMT3A) plays pivotal roles in hematopoietic differentiation. In this study, we followed the hypothesis that alternative splicing of DNMT3A has characteristic epigenetic and functional sequels. Specific DNMT3A transcripts were either down-regulated or overexpressed in human hematopoietic stem and progenitor cells, and this resulted in complementary and transcript-specific DNA methylation and gene expression changes. Functional analysis indicated that, particularly, transcript 2 (coding for DNMT3A2) activates proliferation and induces loss of a primitive immunophenotype, whereas transcript 4 interferes with colony formation of the erythroid lineage. Notably, in acute myeloid leukemia expression of transcript 2 correlates with its in vitro DNA methylation and gene expression signatures and is associated with overall survival, indicating that DNMT3A variants also affect malignancies. Our results demonstrate that specific DNMT3A variants have a distinct epigenetic and functional impact. Particularly, DNMT3A2 triggers hematopoietic differentiation and the corresponding signatures are reflected in acute myeloid leukemia. ER -