Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT)

Yasmine Neirijnck, Antoine Reginensi, Kirsten Y. Renkema, Filippo Massa, Vladimir M. Kozlov, Haroun Dhib, Ernie M.H.F. Bongers, Wout F. Feitz, Albertien M. van Eerde, Veronique Lefebvre, Nine V.A.M. Knoers, Mansoureh Tabatabaei, Herbert Schulz, Helen McNeill, Franz Schaefer, Michael Wegner, Elisabeth Sock, Andreas Schedl

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Congenital abnormalities of the kidney and the urinary tract (CAKUT) belong to the most common birth defects in human, but the molecular basis for the majority of CAKUT patients remains unknown. Here we show that the transcription factor SOX11 is a crucial regulator of kidney development. SOX11 is expressed in both mesenchymal and epithelial components of the early kidney anlagen. Deletion of Sox11 in mice causes an extension of the domain expressing Gdnf within rostral regions of the nephrogenic cord and results in duplex kidney formation. On the molecular level SOX11 directly binds and regulates a locus control region of the protocadherin B cluster. At later stages of kidney development, SOX11 becomes restricted to the intermediate segment of the developing nephron where it is required for the elongation of Henle's loop. Finally, mutation analysis in a cohort of patients suffering from CAKUT identified a series of rare SOX11 variants, one of which interferes with the transactivation capacity of the SOX11 protein. Taken together these data demonstrate a key role for SOX11 in normal kidney development and may suggest that variants in this gene predispose to CAKUT in humans.

Original languageEnglish
Pages (from-to)1142-1153
Number of pages12
JournalKidney International
Volume93
Issue number5
DOIs
StatePublished - May 2018
Externally publishedYes

Keywords

  • CAKUT
  • Sox11
  • duplex kidneys
  • kidney induction
  • nephron

Fingerprint Dive into the research topics of 'Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT)'. Together they form a unique fingerprint.

  • Cite this

    Neirijnck, Y., Reginensi, A., Renkema, K. Y., Massa, F., Kozlov, V. M., Dhib, H., Bongers, E. M. H. F., Feitz, W. F., van Eerde, A. M., Lefebvre, V., Knoers, N. V. A. M., Tabatabaei, M., Schulz, H., McNeill, H., Schaefer, F., Wegner, M., Sock, E., & Schedl, A. (2018). Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT). Kidney International, 93(5), 1142-1153. https://doi.org/10.1016/j.kint.2017.11.026