A novel thrombocytopenia-4-causing CYCS gene variant decreases caspase activity: Three-generation study
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
NU20-08-00137
Ministry of Health, Czech Republic
LX22NPO5102
European Union-Next Generation EU
MUNI/A/1224/2022
Masaryk University
MUNI/11/SUP/22/2020
Masaryk University
CZ.02.1.01/0.0/0.0/16_026/0008448
European Regional Development Fund
FNBr,65269705
Ministry of Health, Czech Republic-conceptual development of research organization
PubMed
39191490
PubMed Central
PMC11637729
DOI
10.1111/bjh.19694
Knihovny.cz E-zdroje
- Klíčová slova
- CRISPR/Cas9, CYCS, caspase, cytochrome c, mitochondria, thrombocytopenia,
- MeSH
- kaspasy * metabolismus genetika MeSH
- lidé MeSH
- rodokmen MeSH
- trombocytopenie * genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- kaspasy * MeSH
The CYCS gene is highly evolutionarily conserved, with only a few pathogenic variants that cause thrombocytopenia-4 (THC4). Here, we report a novel CYCS variant NM_018947.6: c.59C>T [NP_061820.1:p.(Thr20Ile)] segregating with thrombocytopenia in three generations of a Czech family. The phenotype of the patients corresponds to THC4 with platelets of normal size and morphology and dominant inheritance. Intriguingly, a gradual decline in platelet counts was observed across generations. CRISPR/Cas9-mediated gene editing was used to introduce the new CYCS gene variant into a megakaryoblast cell line (MEG-01). Subsequently, the adhesion, shape, size, ploidy, viability, mitochondrial respiration, cytochrome c protein (CYCS) expression, cell surface antigen expression and caspase activity were analysed in cells carrying the studied variant. Interestingly, the variant decreases the expression of CYCS while increasing mitochondrial respiration and the expression of CD9 cell surface antigen. Surprisingly, the variant abates caspase activation, contrasting with previously known effects of other CYCS variants. Some reports indicate that caspases may be involved in thrombopoiesis; thus, the observed dysregulation of caspase activity might contribute to thrombocytopenia. The findings significantly enhance our understanding of the molecular mechanisms underlying inherited thrombocytopenia and may have implications for diagnosis, prognosis and future targeted therapies.
Department of Biology Faculty of Medicine Masaryk University Brno Czechia
Department of Pediatric Hematology and Biochemistry University Hospital Brno Brno Czechia
International Clinical Research Center St Anne's University Hospital Brno Czechia
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