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Staff Profile

Professor Jonathan Higgins

Professor of Eukaryotic Molecular Cell Biology; Director of Non Clinical Fellowships; Theme Lead for Cells, Genes and Molecules

  • Telephone: +44 (0) 191 208 7431
  • Address: Newcastle University Biosciences Institute,
    M2.043, Cookson Building,
    Framlington Place,
    Newcastle upon Tyne,
    Tyne and Wear
    NE2 4HH
Background

Education:

1987-1991 BA, Biochemistry, University of Oxford

1991-1995 DPhil, University of Oxford

Postdoctoral training:

1995-1997 Research Fellow in Medicine, Brigham and Women's Hospital, Harvard Medical School, USA

Previous Appointments:

1997-2002 Instructor in Medicine, Brigham and Women's Hospital, Harvard Medical School, USA

2003-2014 Assistant Professor of Medicine, Brigham and Women's Hospital, Harvard Medical School, USA

2003-2014 Member, Cancer Cell Biology Program, Dana-Farber/Harvard Cancer Center, USA

2006-2014 Member, Biological and Biomedical Sciences Graduate Program, Harvard Medical School, USA

2017-2019 Deputy Dean of Research and Innovation, Faculty of Medical Sciences, Newcastle University

Funding:

Over the years, our work has been funded by a Wellcome Trust Investigator Award, a Royal Society Wolfson Research Merit Award, and by the BBSRC, the MRC, Cancer Research UK/Children with Cancer UK, the National Institutes of Health (USA), the American Cancer Society, the Leukemia and Lymphoma Society, the Crohn's and Colitis Foundation, Worldwide Cancer Research, and the JGW Patterson Foundation.

Google Scholar: Click here.

Research

Our laboratory focuses on cell division, a process that requires a dramatic and highly orchestrated change in cell structure, including the condensation of chromosomes, their alignment on a bipolar spindle, the synchronous movement of exactly half of the chromosomes to opposite poles of the cell, and then cytokinesis (dividing the cell into two).

To accomplish cell division with high fidelity requires tight control of chromosome structure, including the displacement of proteins that might hinder chromosome segregation, and the recruitment of proteins that allow the chromosomes to condense and be “bi-oriented” on the spindle. Through all of this change, the cell also retains markers (“bookmarks”) on chromosomes that can “remember” whether genes are active or inactive so that they can be returned to their original states once cell division is complete. These events must be precisely controlled in location and timing. Our laboratory studies these control mechanisms. In particular, we study how chromatin modifications help determine where and when key regulatory factors can bind to chromosomes.

We are particularly interested in how histone kinases such as Haspin and Aurora B control cell division in human cells, how this process contributes to the generation of cancer and birth defects, and how it can be exploited for disease therapy. In the future, we aim to determine the roles of additional histone modifications in mitosis, to explore their functions in meiosis, and to develop a genome-wide understanding of how these marks are deposited to regulate both chromosome segregation and the inheritance of epigenetic information during cell division. As a spin off as this research, we are also interested in developing new approaches to identify kinases that are responsible for uncharacterised phosphorylation events in cells.

I am Theme Lead for Cells, Genes and Molecules, and a member of the Newcastle University Centre for Cancer.

Teaching


MRes Molecular Cell Biology and Cell Signalling in Health and Disease (Programme Lead)

MMB8008: MRes Cell Cycle Control and Signalling in Health and Disease (Module Lead)

MMB8099: MRes Research Projects

CMB3000: Undergraduate Research Projects

CMB4099: MSci Research Projects

BMS2002: BSc Cell Biology and Disease


Publications