Browsing by Author "Daly, Adrian F."

Now showing 1 - 1 of 1
  • Thumbnail Image
    Item
    Germline loss-of-function PAM variants are enriched in subjects with pituitary hypersecretion
    (Cold Spring Harbor Laboratory, 2023-01-20) Trivellin, Giampaolo; Daly, Adrian F.; Hernández-Ramírez, Laura C.; Araldi, Elisa; Tatsi, Christina; Dale, Ryan K.; Fridell, Gus; Mittal, Arjun; Faucz, Fabio R.; Iben, James R.; Li, Tianwei; Vitali, Eleonora; Stojilkovic, Stanko S.; Kamenicky, Peter; Villa, Chiara; Baussart, Bertrand; Chittiboina, Prashant; Toro, Camilo; Gahl, William A.; Eugster, Erica A.; Naves, Luciana A.; Jaffrain-Rea, Marie-Lise; de Herder, Wouter W.; Neggers, Sebastian Jcmm; Petrossians, Patrick; Beckers, Albert; Lania, Andrea G.; Mains, Richard E.; Eipper, Betty A.; Stratakis, Constantine A.; Pediatrics, School of Medicine
    Pituitary adenomas (PAs) are common, usually benign tumors of the anterior pituitary gland which, for the most part, have no known genetic cause. PAs are associated with major clinical effects due to hormonal dysregulation and tumoral impingement on vital brain structures. Following the identification of a loss-of-function variant (p.Arg703Gln) in the PAM gene in a family with pituitary gigantism, we investigated 299 individuals with sporadic PAs and 17 familial isolated pituitary adenomas kindreds for PAM variants. PAM encodes a multifunctional protein responsible for the essential C-terminal amidation of secreted peptides. Genetic screening was performed by germline and tumor sequencing and germline copy number variation (CNV) analysis. No germline CNVs or somatic single nucleotide variants (SNVs) were identified. We detected seven likely pathogenic heterozygous missense, truncating, and regulatory SNVs. These SNVs were found in sporadic subjects with GH excess (p.Gly552Arg and p.Phe759Ser), pediatric Cushing disease (c.−133T>C and p.His778fs), or with different types of PAs (c.−361G>A, p.Ser539Trp, and p.Asp563Gly). The SNVs were functionally tested in vitro for protein expression and trafficking by Western blotting, for splicing by minigene assays, and for amidation activity in cell lysates and serum samples. These analyses confirmed a deleterious effect on protein expression and/or function. By interrogating 200,000 exomes from the UK Biobank, we confirmed a significant association of the PAM gene and rare PAM SNVs to diagnoses linked to pituitary gland hyperfunction. Identification of PAM as a candidate gene associated with pituitary hypersecretion opens the possibility of developing novel therapeutics based on altering PAM function.