Organization of the pronephric kidney revealed by large-scale gene expression mapping

Daniela Raciti, Luca Reggiani, Lars Geffers, Qiuhong Jiang, Francesca Bacchion, Astrid E Subrizi, Dave Clements, Christopher Tindal, Duncan R Davidson, Brigitte Kaissling, André W Brändli

Research output: Contribution to journalArticleResearchpeer-review

94 Citations (Scopus)


BACKGROUND: The pronephros, the simplest form of a vertebrate excretory organ, has recently become an important model of vertebrate kidney organogenesis. Here, we elucidated the nephron organization of the Xenopus pronephros and determined the similarities in segmentation with the metanephros, the adult kidney of mammals.

RESULTS: We performed large-scale gene expression mapping of terminal differentiation markers to identify gene expression patterns that define distinct domains of the pronephric kidney. We analyzed the expression of over 240 genes, which included members of the solute carrier, claudin, and aquaporin gene families, as well as selected ion channels. The obtained expression patterns were deposited in the searchable European Renal Genome Project Xenopus Gene Expression Database. We found that 112 genes exhibited highly regionalized expression patterns that were adequate to define the segmental organization of the pronephric nephron. Eight functionally distinct domains were discovered that shared significant analogies in gene expression with the mammalian metanephric nephron. We therefore propose a new nomenclature, which is in line with the mammalian one. The Xenopus pronephric nephron is composed of four basic domains: proximal tubule, intermediate tubule, distal tubule, and connecting tubule. Each tubule may be further subdivided into distinct segments. Finally, we also provide compelling evidence that the expression of key genes underlying inherited renal diseases in humans has been evolutionarily conserved down to the level of the pronephric kidney.

CONCLUSION: The present study validates the Xenopus pronephros as a genuine model that may be used to elucidate the molecular basis of nephron segmentation and human renal disease.

Original languageEnglish
Pages (from-to)R84
JournalGenome Biology
Issue number5
Publication statusPublished - 2008
Externally publishedYes


  • Adult
  • Animals
  • Biomarkers
  • Cell Differentiation
  • Chloride-Bicarbonate Antiporters/genetics
  • Gene Expression Regulation, Developmental
  • Humans
  • Kidney/anatomy & histology
  • Kidney Diseases/genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Xenopus Proteins/genetics
  • Xenopus laevis/genetics


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