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  RNA-therapeutic approaches for metabolic pathologies


   MRC Laboratory of Medical Sciences (LMS)

This project is no longer listed on FindAPhD.com and may not be available.

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  Dr S Vernia  No more applications being accepted  Funded PhD Project (Students Worldwide)

About the Project

Analysis of the proteome and transcriptome has demonstrated the existence of a far greater transcriptomic complexity than previously catalogued. RNA alternative splicing contributes significantly to this transcriptional complexity by allowing the generation of multiple splicing variants or isoforms. However, the contribution of specific splicing variants to metabolic homeostasis or to metabolic pathologies has been largely overlooked.

The successful candidate will use both experimental and computational approaches to explore the role of the RNA alternative splicing in metabolic homeostasis in health and in metabolic pathologies such as non-alcoholic fatty liver disease (NAFLD) and hepatocellular carcinoma (HCC).

Projects will involve the use of primary cultures and mouse models of NAFLD and HCC, and multidisciplinary approaches including metabolic phenotyping, in vivo imaging, TMT/MS proteomics and RNA-seq.

Our long-term goal is to identify and characterize RNA alternative splicing programmes and isoforms relevant for human metabolic pathologies to uncover novel targets for the design of diagnostic and therapeutic strategies. 

Further information will be available on the web:

https://lms.mrc.ac.uk/research-group/metabolism-gene-regulation/



Funding Notes

This funding covers tuition fees and also a stipend amounting to £21,000pa paid directly to the student, for 3.5 years in total.
Whilst there are no residency restriction for these studentships, there is more funding available for Home Fee students (including UK nationals and those with settled and pre-settled status until at least April 2026), which make the international studentships highly competitive

References

Vernia S, et al. “An alternative splicing program promotes adipose tissue thermogenesis”. eLife, 2016;5:e17672
Vernia S*, Morel C*, et al. “Excitatory transmission onto AgRP neurons is regulated by cJun NH2-terminal kinase 3 in response to metabolic stress”. eLife, 2016;5:e10031
Vernia S, et al. “Fibroblast growth factor 21 mediates glycemic regulation by hepatic JNK”. Cell Reports. 2016. 14, 1-8, March 15, 2016.
Vernia S, et al. “The PPARα-FGF21 Hormone Axis Contributes to Metabolic Regulation by the Hepatic JNK Signaling Pathway”. Cell Metabolism 20, 1-14, Sept 2, 2014.
Vernia S, et al. “Diet-induced obesity mediated by the JNK/DIO2 signal transduction pathway”. Genes and Development. 2013 Nov 1;27(21):2345-55.