| Literature DB >> 28871137 |
A E Marneth1, K H M Prange2, A S A Al Hinai3, S M Bergevoet1, N Tesi2, E M Janssen-Megens2, B Kim2, N Sharifi2, M L Yaspo4, J Kuster2, M A Sanders3, E C G Stoetman3, J Knijnenburg5, T C J M Arentsen-Peters6, C M Zwaan6, H G Stunnenberg2, M M van den Heuvel-Eibrink6,7, T Haferlach8, M Fornerod6, J H Jansen1, P J M Valk3, B A van der Reijden1, J H A Martens2.
Abstract
Overexpression of the BRE (brain and reproductive organ-expressed) gene defines a distinct pediatric and adult acute myeloid leukemia (AML) subgroup. Here we identify a promoter enriched for active chromatin marks in BRE intron 4 causing strong biallelic expression of a previously unknown C-terminal BRE transcript. This transcript starts with BRE intron 4 sequences spliced to exon 5 and downstream sequences, and if translated might code for an N terminally truncated BRE protein. Remarkably, the new BRE transcript was highly expressed in over 50% of 11q23/KMT2A (lysine methyl transferase 2A)-rearranged and t(8;16)/KAT6A-CREBBP cases, while it was virtually absent from other AML subsets and normal tissues. In gene reporter assays, the leukemia-specific fusion protein KMT2A-MLLT3 transactivated the intragenic BRE promoter. Further epigenome analyses revealed 97 additional intragenic promoter marks frequently bound by KMT2A in AML with C-terminal BRE expression. The corresponding genes may be part of a context-dependent KMT2A-MLLT3-driven oncogenic program, because they were higher expressed in this AML subtype compared with other groups. C-terminal BRE might be an important contributor to this program because in a case with relapsed AML, we observed an ins(11;2) fusing CHORDC1 to BRE at the region where intragenic transcription starts in KMT2A-rearranged and KAT6A-CREBBP AML.Entities:
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Year: 2017 PMID: 28871137 DOI: 10.1038/leu.2017.280
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528