DIS3 Variants are Associated with Primary Ovarian Insufficiency: Importance of Transcription/Translation in Oogenesis.
Erica Boiman JohnstoneBushra GorsiEmily CoelhoBarry MooreAshley M FarrAmber R CooperElaine R MardisAleksander RajkovicClement Y ChowMark YandellCorrine K WeltPublished in: The Journal of clinical endocrinology and metabolism (2023)
Compound heterozygous variants in highly conserved amino acids in DIS3 and failure of oocyte production in a functional model suggest that mutations in DIS3 cause POI. DIS3 is a 3' to 5' exoribonuclease that is the catalytic subunit of the exosome involved in RNA degradation and metabolism in the nucleus. The findings provide further evidence that mutations in genes important for transcription and translation are associated with POI.