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Expression of FMRpolyG in peripheral blood mononuclear cells of women with fragile X mental retardation 1 gene premutation

Fragile X-associated primary ovarian insufficiency (FXPOI) is characterized by oligo/amenorrhea and hypergonadotropic hypogonadism and is caused by the expansion of the CGG repeat in the 5′UTR of Fragile X Mental Retardation 1 (FMR1). Approximately 20% of women carrying an FMR1 premutation (PM) alle...

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Hauptverfasser: Nguyen, Xuan Phuoc (VerfasserIn) , Vilkaite, Adriana (VerfasserIn) , Messmer, Birgitta (VerfasserIn) , Dietrich, Jens Erik (VerfasserIn) , Hinderhofer, Katrin (VerfasserIn) , Schäkel, Knut (VerfasserIn) , Strowitzki, Thomas (VerfasserIn) , Rehnitz, Julia (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1 March 2022
In: Genes
Year: 2022, Jahrgang: 13, Heft: 3, Pages: 1-3
ISSN:2073-4425
DOI:10.3390/genes13030451
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.3390/genes13030451
Verlag, kostenfrei, Volltext: https://www.mdpi.com/2073-4425/13/3/451
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Verfasserangaben:Xuan Phuoc Nguyen, Adriana Vilkaite, Birgitta Messmer, Jens E. Dietrich, Katrin Hinderhofer, Knut Schäkel, Thomas Strowitzki and Julia Rehnitz
Beschreibung
Zusammenfassung:Fragile X-associated primary ovarian insufficiency (FXPOI) is characterized by oligo/amenorrhea and hypergonadotropic hypogonadism and is caused by the expansion of the CGG repeat in the 5′UTR of Fragile X Mental Retardation 1 (FMR1). Approximately 20% of women carrying an FMR1 premutation (PM) allele (55-200 CGG repeat) develop FXPOI. Repeat Associated Non-AUG (RAN)-translation dependent on the variable CGG-repeat length is thought to cause FXPOI, due to the production of a polyglycine-containing FMR1 protein, FMRpolyG. Peripheral blood monocyte cells (PBMCs) and granulosa cells (GCs) were collected to detect FMRpolyG and its cell type-specific expression in FMR1 PM carriers by immunofluorescence staining (IF), Western blotting (WB), and flow cytometric analysis (FACS). For the first time, FMRpolyG aggregates were detected as ubiquitin-positive inclusions in PBMCs from PM carriers, whereas only a weak signal without inclusions was detected in the controls. The expression pattern of FMRpolyG in GCs was comparable to that in the lymphocytes. We detected FMRpolyG as a 15- to 25-kDa protein in the PBMCs from two FMR1 PM carriers, with 124 and 81 CGG repeats. Flow cytometric analysis revealed that FMRpolyG was significantly higher in the T cells from PM carriers than in those from non-PM carriers. The detection of FMRpolyG aggregates in the peripheral blood and granulosa cells of PM carriers suggests that it may have a toxic potential and an immunological role in ovarian damage in the development of FXPOI.
Beschreibung:Gesehen am 05.04.2022
Beschreibung:Online Resource
ISSN:2073-4425
DOI:10.3390/genes13030451

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