Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • News & Views
  • Published:

GENETICS

Glomerular and tubulointerstitial eQTLs for genomic discovery

A new study discovered thousands of expression quantitative trait loci (eQTLs) in the renal glomerular and tubulointerstitial compartments and integrated these data with other omics data sets to identify genes with roles in the pathogenesis of chronic kidney disease. This report reinforces the necessity of using compartment-derived eQTLs to advance kidney genomic discovery.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Compartment-based eQTL discovery.

References

  1. Qiu, C. et al. Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. Nat. Med. 24, 1721–1731 (2018).

    Article  CAS  Google Scholar 

  2. Varshney, A. et al. Genetic regulatory signatures underlying islet gene expression and type 2 diabetes. Proc. Natl Acad. Sci. USA 114, 2301–2306 (2017).

    Article  CAS  Google Scholar 

  3. Bhalala, O. G. et al. Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue. PLOS Genet. 14, e1007607 (2018).

    Article  Google Scholar 

  4. GTEx Consortium. Genetic effects on gene expression across human tissues. Nature 550, 204–213 (2017).

    Article  Google Scholar 

  5. Gamazon, E. R. et al. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nat. Genet. 50, 956–967 (2018).

    Article  CAS  Google Scholar 

  6. Wheeler, H. E. et al. Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging. PLOS Genet. 5, e1000685 (2009).

    Article  Google Scholar 

  7. Sandholm, N. et al. New susceptibility loci associated with kidney disease in type 1 diabetes. PLOS Genet. 8, e1002921 (2012).

    Article  CAS  Google Scholar 

  8. Ko, Y. A. et al. Genetic-variation-driven gene-expression changes highlight genes with important functions for kidney disease. Am. J. Hum. Genet. 100, 940–953 (2017).

    Article  CAS  Google Scholar 

  9. Gillies, C. E. et al. An eQTL landscape of kidney tissue in human nephrotic syndrome. Am. J. Hum. Genet. 103, 232–244 (2018).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The author’s work is supported by the Charles Woodson Clinical Research Fund, the Ravitz Foundation and by National Institutes of Health RO1-DK108805.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Matthew G. Sampson.

Ethics declarations

Competing interests

The author declares no competing interests.

Additional information

Related links

NephQTL: http://nephqtl.org

Human kidney eQTL atlas: http://susztaklab.com/eqtl

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sampson, M.G. Glomerular and tubulointerstitial eQTLs for genomic discovery. Nat Rev Nephrol 15, 3–4 (2019). https://doi.org/10.1038/s41581-018-0089-0

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41581-018-0089-0

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing