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Biography

Rachel studied for her PhD with Dr Patrick Varga-Weisz at the Babraham Institute. Her research focussed on histone crotonylation, a type of epigenetic switch that promotes gene expression and is chemically related to metabolites in the cell gut microbiome. Bacteria in our gut ferment fibre in our diet to produce short chain fatty acids that can be added onto histones to produce epigenetic switches such as histone crotonylation and acetylation. Together with her colleagues, she found that when the gut microbiome was depleted in mice by antibiotics, histone crotonylation and related modifications were reduced in intestinal epithelial cells along with changes to which genes were expressed. This suggested that the gut bacteria, could use these biproducts of digesting fibre to influence the function of the cells lining our intestine. As part of this project, Rachel spent 6-months at the University of Campinas in Brazil, at Marco Aurélio Ramirez Vinolo's group that had expertise in short chain fatty acids and the gut immune system.

After her PhD, Rachel did a short research project on sperm production with Dr Kazuyuki Ohbo, at the Yokohama City University in Japan, where she investigated how knock-out of the protein Wfdc5a resulted in infertile male mice. Rachel then did a Post-doctoral scholarship at the University of California Irvine, where she helped to identify that in mice with loss of one copy of Apc clock disruption drives loss of both copies of the Apc gene which hyperactivates Wnt signalling and accelerates tumour progression. She also compared gut microbiome composition between clock disrupted and cancer mice, finding that common groups of bacteria present in the gut microbiome including Bacteroides, Helicobacter and Megasphaera are altered in both conditions. After working as a Senior Scientist on intestinal ageing at Altos Labs, Rachel joined the Unit in November 2024 and is currently working to share MRC Toxicology Unit science and research to people of all ages and backgrounds. She is passionate about sharing scientific knowledge to increase the impact of research and encourage people to be excited about biology!

Rachel is responsible for the Unit's communication activities, including news, press, digital, social media, website and branding. She also leads on the public engagement strategy for the Unit to increase public awareness and understanding of the Unit’s research.

Unit news | Public Engagement

 

Publications

Key publications: 

Key publications

Fellows, R. C.*, Chun, S. K., Larson, N., ... Masri, S., (2024) Disruption of the Intestinal Clock drives Dysbiosis and Impaired Barrier Function in Colorectal Cancer. Science Advances. https://doi.org/10.1126/sciadv.ado1458

Tomizawa, S., Fellows, R. C., … Ohbo, K., (2024) A non-canonical bivalent gene Wfdc15a controls spermatogenic protease and immune homeostasis. Development. https://doi.org/10.1242/dev.202834

Chun, S. K.*, Fortin, B. M.*, Fellows, R. C.*, … Masri, S. (2022). Disruption of the circadian clock drives Apc loss of heterozygosity to accelerate colorectal cancer. Science Advances, 1–20. https://doi.org/10.1126/sciadv.abo2389

Fellows, R.*, … Vinolo, M. A. R., Varga-Weisz, P. (2018). Microbiota derived short chain fatty acids promote histone crotonylation in the colon through histone deacetylases. Nature Communications, 9(105), 1–15. https://doi.org/10.1038/s41467-017-02651-5

 

Science Communication and Public Engagement Manager

Contact Details

MRC Toxicology Unit
Gleeson Building
Tennis Court Road
Cambridge

CB2 1QR

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