Contact information
Colleges
Nicholas Crump
Kay Kendall Leukaemia Fund Intermediate Research Fellow
I completed my DPhil in the lab of Louis Mahadevan, Department of Biochemistry, where I studied the role of dynamic histone acetylation in the control of gene expression. I joined the Milne lab in 2016, where my research is directed towards understanding the role of enhancers in leukaemia, focusing on MLL-AF4 ALL. I am interested in using this knowledge to identify novel targets to disrupt epigenetic regulation as a therapeutic intervention.
I use a variety of high-throughput techniques to understand the regulation of chromatin and gene expression, including ChIP-seq (and small cell number techniques such as ChIPmentation), ATAC-seq and RNA-seq. In addition, I use the 3C technology Next Generation Capture-C to investigate the physical association of enhancers and promoters, and how this is regulated. I also have an interest in the role of the immune system in cancer targeting, in collaboration with the Multi-dimensional Innate and Adaptive Immune Responses lab (HIU), particularly how cancer cells can manipulate the extracellular environment to suppress immune activity.
In addition to my research activities, I teach topics in molecular cell biology for Biochemistry undergraduates at Oxford. I was a stipendiary lecturer at Worcester College from 2014-2019, and I continue to be involved in tutorials and admissions at Worcester and a number of other colleges.
Recent publications
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PAF1 and FACT cooperate with MLL-AF4 to drive enhancer activity in leukemia
Preprint
Crump NT. et al, (2022)
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Alkaline nucleoplasm facilitates contractile gene expression in the mammalian heart.
Journal article
Hulikova A. et al, (2022), Basic Res Cardiol, 117
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Potent, p53-independent induction of NOXA sensitizes MLL-rearranged B-cell acute lymphoblastic leukemia cells to venetoclax.
Journal article
Fidyt K. et al, (2022), Oncogene, 41, 1600 - 1609
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A human fetal liver-derived infant MLL-AF4 acute lymphoblastic leukemia model reveals a distinct fetal gene expression program
Journal article
Rice S. et al, (2021), Nature Communications, 12
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Defining genome architecture at base-pair resolution.
Journal article
Hua P. et al, (2021), Nature, 595, 125 - 129