Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking

Hum Mol Genet. 2011 Jan 15;20(2):301-11. doi: 10.1093/hmg/ddq465. Epub 2010 Oct 29.

Abstract

Renal tubular dysgenesis (RTD) is a recessive autosomal disease characterized by persistent fetal anuria and perinatal death. During the systematic screening of mutations of the different genes of the renin-angiotensin system associated with RTD, two missense mutations in the renin gene were previously identified, the first affects one of the two catalytic aspartates (D38N) of renin, and the second, S69Y, is located upstream of the 'flap', a mobile β-hairpin structure which covers the substrate-binding site of renin. Here we report a novel renin mutation leading to the duplication of the tyrosine residue Y15dup, homologous to Y9 in some other aspartyl proteases, which seems to play a crucial role along the activation pathway. The biochemical and cellular mechanisms underlying renin inactivation were investigated. We expressed prorenin constructs harboring the identified point mutations in two established cell lines, able (AtT-20 cells) or unable (CHO cells) to process prorenin to renin and we evaluated the cellular localization of renin mutants and their functional properties. All three mutants were misfolded to different levels, were enzymatically inactive and exhibited abnormal intracellular trafficking. We suggest a misfolding of Y15dup renin, a partial misfolding of D38N prorenin and a misfolding of S69Y prorenin leading to complete absence of secretion. The structural consequences of the renin mutations were estimated by molecular modeling, which suggested some important structural alterations. This is the first characterization of the mechanisms underlying loss of renin function in RTD.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CHO Cells
  • Cell Line
  • Cricetinae
  • Cricetulus
  • Female
  • Humans
  • Kidney Tubules, Proximal / abnormalities
  • Kidney Tubules, Proximal / pathology
  • Models, Molecular
  • Molecular Sequence Data
  • Point Mutation*
  • Pregnancy
  • Protein Structure, Tertiary
  • Protein Transport*
  • Recombinant Proteins / metabolism
  • Renin / analysis
  • Renin / chemistry
  • Renin / genetics*
  • Renin / metabolism*
  • Sequence Alignment
  • Urogenital Abnormalities / genetics*
  • Urogenital Abnormalities / pathology*

Substances

  • Recombinant Proteins
  • Renin

Supplementary concepts

  • Allanson Pantzar McLeod syndrome