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http://purl.uniprot.org/citations/33297935http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
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Background

FINCA disease is a pediatric cerebropulmonary disease caused by variants in the NHL repeat-containing 2 (NHLRC2) gene. Neurological symptoms are among the first manifestations of FINCA disease, but the consequences of NHLRC2 deficiency in the central nervous system are currently unexplored.

Methods

The orthologous mouse gene is essential for development, and its complete loss leads to early embryonic lethality. In the current study, we used CRISPR/Cas9 to generate an Nhlrc2 knockin (KI) mouse line, harboring the FINCA patient missense mutation (c.442G > T, p.Asp148Tyr). A FINCA mouse model, resembling the compound heterozygote genotype of FINCA patients, was obtained by crossing the KI and Nhlrc2 knockout mouse lines. To reveal NHLRC2-interacting proteins in developing neurons, we compared cortical neuronal precursor cells of E13.5 FINCA and wild-type mouse embryos by two-dimensional difference gel electrophoresis.

Results

Despite the significant decrease in NHLRC2, the mice did not develop severe early onset multiorgan disease in either sex. We discovered 19 altered proteins in FINCA neuronal precursor cells; several of which are involved in vesicular transport pathways and actin dynamics which have been previously reported in other cell types including human to have an association with dysfunctional NHLRC2. Interestingly, isoform C2 of hnRNP C1/C2 was significantly increased in both developing neurons and the hippocampus of adult female FINCA mice, connecting NHLRC2 dysfunction with accumulation of RNA binding protein.

Conclusions

We describe here the first NHLRC2-deficient mouse model to overcome embryonic lethality, enabling further studies on predisposing and causative mechanisms behind FINCA disease. Our novel findings suggest that disrupted RNA metabolism may contribute to the neurodegeneration observed in FINCA patients."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.org/dc/terms/identifier"doi:10.1186/s10020-020-00245-4"xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Tuominen H."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Ohlmeier S."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Tanila H."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"McKerlie C."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Hinttala R."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Uusimaa J."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Hallman M."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Hiltunen A.E."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Kaarteenaho R."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Govindan S."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Hiltunen J."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Kangas S.M."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/author"Pietila I."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/name"Mol Med"xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/pages"123"xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/title"Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCA disease."xsd:string
http://purl.uniprot.org/citations/33297935http://purl.uniprot.org/core/volume"26"xsd:string
http://purl.uniprot.org/citations/33297935http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33297935
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http://purl.uniprot.org/uniprot/#_A0A494BBH3-mappedCitation-33297935http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33297935
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