School of Life Sciences

Alpha-defensin haplotypes and IgA nephropathy risk

 

Fact file

Duration Three to four years full-time
Eligibility Self-funded; Home, EU or International Students
Supervisor(s)

Professor John Armour

Professor Olivier Hanotte

Application deadline  No deadline
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Research Division

Find out more about our cells, organisms and molecular genetics research division

 


About the project

The human alpha-defensin genes DEFA1 and DEFA3 encode short antimicrobial peptides that are important components of the innate immune system, and are subject to copy number variation (CNV) with individuals having between 3 and 18 copies. Association studies have demonstrated that genetic variants near to DEFA1 and DEFA3 are associated with the serious kidney disease IgA nephropathy. In collaboration with groups in Guangzhou and Singapore, Prof Armour’s group have shown that the association signal can be attributed to the CNV region, with two specific variants implicated: one variant provides protection against IgA nephropathy and is specific to Asian populations; the second variant predisposes to IgA nephropathy in both Europeans and Asians. The structures of the variants implicated in IgA nephropathy, and the features leading to the associations with disease, are currently unknown. This project will combine detailed analysis of publicly available sequence data (from the 1000 Genomes Project), novel approaches to long-read sequencing (using Nanopore devices) and examination of datasets from affected individuals to understand how alpha-defensin variants predispose to IgA nephropathy. This project would give the student experience in the analysis of genetic variation relevant to disease, high-resolution characterisation of copy number variation, and manipulation of large datasets.

Funding notes

This project is available to self-funded students. Home applicants should contact the supervisor to determine the current funding status for this project. EU applicants should visit the Graduate School webpages for information on specific EU scholarships. International applicants should visit our International Research Scholarships page for information regarding fees and funding at the University.

References

  • Ai, Z., Li, M., Liu, W., Foo, J.N., Mansouri, O., Yin, P., Zhou, Q., Tang, X., Dong, X., Feng, S., Xu, R., Zhong, Z., Chen, J., Wan, J., Lou, T., Yu, J., Zhou, Q., Fan, J., Mao, H., Gale, D., Barratt, J., Armour, J.A., Liu, J. and Yu, X. (2016). Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction. Science Translational Medicine. 8, 345ra88.

  • Black H.A., Khan, F.F., Tyson, J. and Armour, J.A.L. (2014) Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus. BMC Genomics 15, 614

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Alpha-defensin haplotypes and IgA nephropathy risk

School of Life Sciences

University of Nottingham
Medical School
Queen's Medical Centre
Nottingham NG7 2UH

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