MLL-AF4 cooperates with PAF1 and FACT to drive high-density enhancer interactions in leukemia

Author:

Crump Nicholas T.ORCID,Smith Alastair L.ORCID,Godfrey Laura,Dopico-Fernandez Ana M.ORCID,Denny Nicholas,Harman Joe R.ORCID,Hamley Joseph C.,Jackson Nicole E.ORCID,Chahrour CatherineORCID,Riva Simone,Rice Siobhan,Kim JaehoonORCID,Basrur Venkatesha,Fermin Damian,Elenitoba-Johnson Kojo,Roeder Robert G.ORCID,Allis C. DavidORCID,Roberts Irene,Roy AninditaORCID,Geng Huimin,Davies James O. J.,Milne Thomas A.ORCID

Abstract

AbstractAberrant enhancer activation is a key mechanism driving oncogene expression in many cancers. While much is known about the regulation of larger chromosome domains in eukaryotes, the details of enhancer-promoter interactions remain poorly understood. Recent work suggests co-activators like BRD4 and Mediator have little impact on enhancer-promoter interactions. In leukemias controlled by the MLL-AF4 fusion protein, we use the ultra-high resolution technique Micro-Capture-C (MCC) to show that MLL-AF4 binding promotes broad, high-density regions of enhancer-promoter interactions at a subset of key targets. These enhancers are enriched for transcription elongation factors like PAF1C and FACT, and the loss of these factors abolishes enhancer-promoter contact. This work not only provides an additional model for how MLL-AF4 is able to drive high levels of transcription at key genes in leukemia but also suggests a more general model linking enhancer-promoter crosstalk and transcription elongation.

Funder

RCUK | MRC | Medical Research Foundation

RCUK | Medical Research Council

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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