Biallelic FANCA variants detected in sisters with isolated premature ovarian insufficiency

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Tucker, Elena J. | F. Sharp, Michael | Lokchine, Anna | Bell, Katrina M | S. Palmer, Catherine | Kline, Brianna L | Robevska, Gorjana | van den Bergen, Jocelyn | Dulon, Jérôme | Stojanovski, Diana | Ayers, Katie | Touraine, Philippe | Crismani, Wayne | Jaillard, Sylvie | Sinclair, Andrew

Edité par CCSD ; Wiley -

International audience. Premature ovarian insufficiency is a common form of female infertility affecting up to 4% of women and characterised by amenorrhea with elevated gonadotropin before the age of 40. Oocytes require controlled DNA breakage and repair for homologous recombination and the maintenance of oocyte integrity. Biallelic disruption of the DNA damage repair gene, Fanconi anemia complementation group A (FANCA), is a common cause of Fanconi anaemia, a syndrome characterised by bone marrow failure, cancer predisposition, physical anomalies and POI. There is ongoing dispute about the role of heterozygous FANCA variants in POI pathogenesis, with insufficient evidence supporting causation. Here, we have identified biallelic FANCA variants in French sisters presenting with POI, including a novel missense variant of uncertain significance and a likely pathogenic deletion that initially evaded detection. Functional studies indicated no discernible effect on DNA damage sensitivity in patient lymphoblasts. These novel FANCA variants add evidence that heterozygous loss of one allele is insufficient to cause DNA damage sensitivity and POI. We propose that intragenic deletions, that are relatively common in FANCA, may be missed without careful analysis, and could explain the presumed causation of heterozygous variants. Accurate variant curation is critical to optimise patient care and outcomes.

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