Renal agenesis in Kallmann syndrome: a network approach

Ann Hum Genet. 2014 Nov;78(6):424-33. doi: 10.1111/ahg.12079. Epub 2014 Sep 17.

Abstract

Kallmann syndrome (KS) is defined by the combination of isolated hypogonadotrophic hypogonadism (IHH) and anosmia, with renal agenesis occurring in 30% of KS cases with KAL1 gene mutations. Unlike other KS-related disorders, renal agenesis cannot be directly associated with mutations in the KAL1 gene. We hypothesized that protein interaction networks may suggest a link between genes currently known to be associated with KS on the one hand and those associated with renal agenesis on the other hand. We created a STRING protein interaction network from KS-related genes and renal-agenesis-associated genes and analyzed it with Cytoscape 3.0.1 network software. The STRING protein interaction network provided a conceptual framework for current knowledge on the subject of renal morphogenesis in Kallmann syndrome. In addition, STRING and Cytoscape 3.0.1 software identified new potential KS renal-aplasia-associated genes (PAX2, BMP4, and SOX10). The use of protein-protein interaction networks and network analysis tools provided interesting insights and possible directions for future studies on the subject of renal aplasia in Kallmann syndrome.

Keywords: Kallmann syndrome; anosmin‐1; protein–protein interactions; renal agenesis.

MeSH terms

  • Cluster Analysis
  • Computational Biology
  • Congenital Abnormalities / genetics*
  • Humans
  • Kallmann Syndrome / genetics*
  • Kidney / abnormalities*
  • Kidney Diseases / congenital*
  • Kidney Diseases / genetics
  • Monte Carlo Method
  • Protein Interaction Maps*
  • Software

Supplementary concepts

  • Hereditary renal agenesis