Mutation-induced LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome

Cell Rep. 2024 Jul 23;43(7):114448. doi: 10.1016/j.celrep.2024.114448. Epub 2024 Jul 13.

Abstract

Noonan syndrome patients harboring causative variants in LZTR1 are particularly at risk to develop severe and early-onset hypertrophic cardiomyopathy. In this study, we investigate the mechanistic consequences of a homozygous variant LZTR1L580P by using patient-specific and CRISPR-Cas9-corrected induced pluripotent stem cell (iPSC) cardiomyocytes. Molecular, cellular, and functional phenotyping in combination with in silico prediction identify an LZTR1L580P-specific disease mechanism provoking cardiac hypertrophy. The variant is predicted to alter the binding affinity of the dimerization domains facilitating the formation of linear LZTR1 polymers. LZTR1 complex dysfunction results in the accumulation of RAS GTPases, thereby provoking global pathological changes of the proteomic landscape ultimately leading to cellular hypertrophy. Furthermore, our data show that cardiomyocyte-specific MRAS degradation is mediated by LZTR1 via non-proteasomal pathways, whereas RIT1 degradation is mediated by both LZTR1-dependent and LZTR1-independent pathways. Uni- or biallelic genetic correction of the LZTR1L580P missense variant rescues the molecular and cellular disease phenotype, providing proof of concept for CRISPR-based therapies.

Keywords: CP: Cell biology; CP: Metabolism; CRISPR/Cas9; LZTR1; Noonan syndrome; RAS-MAPK signaling; cardiomyocytes; disease modeling; hypertrophic cardiomyopathy; iPSCs; protein polymerization.

MeSH terms

  • CRISPR-Cas Systems / genetics
  • Cardiomyopathy, Hypertrophic / genetics
  • Cardiomyopathy, Hypertrophic / metabolism
  • Cardiomyopathy, Hypertrophic / pathology
  • Genes, Recessive
  • Humans
  • Induced Pluripotent Stem Cells* / metabolism
  • Induced Pluripotent Stem Cells* / pathology
  • Mutation / genetics
  • Mutation, Missense
  • Myocytes, Cardiac* / metabolism
  • Myocytes, Cardiac* / pathology
  • Noonan Syndrome* / genetics
  • Noonan Syndrome* / metabolism
  • Noonan Syndrome* / pathology
  • Phenotype
  • Polymerization
  • Protein Multimerization
  • Proteolysis
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • ras Proteins* / genetics
  • ras Proteins* / metabolism

Substances

  • LZTR1 protein, human
  • RIT1 protein, human
  • ras Proteins
  • Transcription Factors
  • MRAS protein, human