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Wilms' tumour 1 (WT1) in development, homeostasis and disease.

Nicholas D Hastie
Published in: Development (Cambridge, England) (2017)
The study of genes mutated in human disease often leads to new insights into biology as well as disease mechanisms. One such gene is Wilms' tumour 1 (WT1), which plays multiple roles in development, tissue homeostasis and disease. In this Primer, I summarise how this multifaceted gene functions in various mammalian tissues and organs, including the kidney, gonads, heart and nervous system. This is followed by a discussion of our current understanding of the molecular mechanisms by which WT1 and its two major isoforms regulate these processes at the transcriptional and post-transcriptional levels.
Keyphrases
  • gene expression
  • genome wide
  • heart failure
  • endothelial cells
  • copy number
  • genome wide identification
  • dna methylation
  • atrial fibrillation
  • oxidative stress