Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene

Genes (Basel). 2022 Aug 29;13(9):1558. doi: 10.3390/genes13091558.

Abstract

Pathogenic variants of zinc finger C4H2-type containing (ZC4H2) on the X chromosome cause a group of genetic diseases termed ZC4H2-associated rare disorders (ZARD), including Wieacker-Wolff Syndrome (WRWF) and Female-restricted Wieacker-Wolff Syndrome (WRWFFR). In the current study, a de novo c.352C>T (p.Gln118*) mutation in ZC4H2 (NM_018684.4) was identified in a female neonate born with severe arthrogryposis multiplex congenita (AMC) and Pierre-Robin sequence (cleft palate and micrognathia). Plasmids containing the wild-type (WT), mutant-type (MT) ZC4H2, or GFP report gene (N) were transfected in 293T cell lines, respectively. RT-qPCR and western blot analysis showed that ZC4H2 protein could not be detected in the 293T cells transfected with MT ZC4H2. The RNA seq results revealed that the expression profile of the MT group was similar to that of the N group but differed significantly from the WT group, indicating that the c.352C>T mutation resulted in the loss of function of ZC4H2. Differentially expressed genes (DEGs) enrichment analysis showed that c.352C>T mutation inhibited the expression levels of a series of genes involved in the oxidative phosphorylation pathway. Subsequently, expression levels of ZC4H2 were knocked down in neural stem cells (NSCs) derived from induced pluripotent stem cells (iPSCs) by lentiviral-expressed small hairpin RNAs (shRNAs) against ZC4H2. The results also demonstrated that decreasing the expression of ZC4H2 significantly reduced the growth of NSCs by affecting the expression of genes related to the oxidative phosphorylation signaling pathway. Taken together, our results strongly suggest that ZC4H2 c.352C>T (p.Gln118*) mutation resulted in the loss of protein function and caused WRWFFR.

Keywords: WRWF; WRWFFR; ZC4H2; nonsense mutation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apraxias
  • Carrier Proteins / genetics
  • Codon, Nonsense*
  • Contracture
  • Female
  • Genetic Diseases, X-Linked
  • Intracellular Signaling Peptides and Proteins / genetics
  • Muscular Atrophy
  • Nuclear Proteins* / genetics
  • Ophthalmoplegia
  • Phenotype

Substances

  • Carrier Proteins
  • Codon, Nonsense
  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins

Supplementary concepts

  • Wieacker syndrome

Grants and funding

This research was funded by the National Key Research and Development Program of China, Grand/Award number: (2019YFA0801402, 2016YFC1000503 and 2016YFC0905102); the National Basic Research Program of China, Grand/Award number: (2014CB964700); the National Natural Science Foundation of China, Grant/Award number: (31871484); Shanghai key clinical specialty project, Grand/Award number: (shslczdzk05705); Shanghai Top Priority Key Discipline Project, Grant/Award number: (2017ZZ02019); Innovative Research Team of High-Level Local Universities in Shanghai, Grand/Award number: (SHSMU-ZDCX20212200).