CBFA2T3-GLIS2 mediates transcriptional regulation of developmental pathways through a gene regulatory network

CBFA2T3-GLIS2 is a fusion oncogene found in pediatric acute megakaryoblastic leukemia that is associated with a poor prognosis. We establish a model of CBFA2T3-GLIS2 driven acute megakaryoblastic leukemia that allows the distinction of fusion specific changes from those that reflect the megakaryoblast lineage of this leukemia. Using this model, we map fusion genome wide binding that in turn imparts the characteristic transcriptional signature. A network of transcription factor genes bound and upregulated by the fusion are found to have downstream effects that result in dysregulated signaling of developmental pathways including NOTCH, Hedgehog, TGFβ, and WNT. Transcriptional regulation is mediated by homo-dimerization and binding of the ETO transcription factor through the nervy homology region 2. Loss of nerve homology region 2 abrogated the development of leukemia, leading to downregulation of JAK/STAT, Hedgehog, and NOTCH transcriptional signatures. These data contribute to the understanding of CBFA2T3-GLIS2 mediated leukemogenesis and identify potential therapeutic vulnerabilities for future studies.

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Publication Details

Journal
Nature Communications
Published
2024-10-09
DOI
https://doi.org/10.1038/s41467-024-53158-9
Citations
4
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.94

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article

CBFA2T3-GLIS2 mediates transcriptional regulation of developmental pathways through a gene regulatory network

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4 citations
Nature Communications
Ubiquitin and proteasome pathways
0.94
article

CBFA2T3-GLIS2 mediates transcriptional regulation of developmental pathways through a gene regulatory network

Binay K. Sahoo, Anitria Cotton, Tanja A. Grüber, Jinjun Dang, Taylor L. Wilson, Elizabeth A.R. Garfinkle, Sharnise Mitchell, Mohammad Balood, Pratima Nallagatla, Camryn Franke
article en
4 citations

Abstract

CBFA2T3-GLIS2 is a fusion oncogene found in pediatric acute megakaryoblastic leukemia that is associated with a poor prognosis. We establish a model of CBFA2T3-GLIS2 driven acute megakaryoblastic leukemia that allows the distinction of fusion specific changes from those that reflect the megakaryoblast lineage of this leukemia. Using this model, we map fusion genome wide binding that in turn imparts the characteristic transcriptional signature. A network of transcription factor genes bound and upregulated by the fusion are found to have downstream effects that result in dysregulated signaling of developmental pathways including NOTCH, Hedgehog, TGFβ, and WNT. Transcriptional regulation is mediated by homo-dimerization and binding of the ETO transcription factor through the nervy homology region 2. Loss of nerve homology region 2 abrogated the development of leukemia, leading to downregulation of JAK/STAT, Hedgehog, and NOTCH transcriptional signatures. These data contribute to the understanding of CBFA2T3-GLIS2 mediated leukemogenesis and identify potential therapeutic vulnerabilities for future studies.

Nature CommunicationsVol. 15(1)
St. Jude Children's Research Hospital (US), Stanford Medicine (US), Stanford University (US)
Vanderbilt University, St. Jude Children's Research Hospital, American Lebanese Syrian Associated Charities, Vanderbilt University Medical Center, Universiteit Gent
Openalex Percentile: Top 25%
Ubiquitin and proteasome pathways
0.94
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