Open AccessIdentification and Functional Characterization of Three NoLS (Nucleolar Localisation Signals) Mutations of the CDC73 Gene
Author(s) -
Valerio Pazienza,
Annamaria la Torre,
Filomena Baorda,
Michela Alfarano,
Massimiliano Chetta,
Lucia Anna Muscarella,
Claudia Battista,
Massimiliano Copetti,
Dieter Kotzot,
Klaus Kapelari,
Dalia AlAbdulrazzaq,
Kusiel Perlman,
Etienne Sochett,
David E. C. Cole,
Fabio Pellegrini,
Lucie Canaff,
Geoffrey N. Hendy,
Leonardo D’Agruma,
Leopoldo Zelante,
Massimo Carella,
Alfredo Scillitani,
Vito Guarnieri
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0082292
Subject(s) - primary hyperparathyroidism , biology , mutation , germline mutation , microbiology and biotechnology , parathyroid carcinoma , transfection , somatic cell , gene mutation , mutant , cancer research , germline , gene , genetics , endocrinology
Hyperparathyroidism Jaw-Tumour Syndrome (HPT-JT) is characterized by primary hyperparathyroidism (PHPT), maxillary/mandible ossifying fibromas and by parathyroid carcinoma in 15% of cases. Inactivating mutations of the tumour suppressor CDC73/HRPT2 gene have been found in HPT-JT patients and also as genetic determinants of sporadic parathyroid carcinoma/atypical adenomas and, rarely, typical adenomas, in familial PHPT. Here we report the genetic and molecular analysis of the CDC73/HRPT2 gene in three patients affected by PHPT due to atypical and typical parathyroid adenomas, in one case belonging to familial PHPT. Flag-tagged WT and mutant CDC73/HRPT2 proteins were transiently transfected in HEK293 cells and functional assays were performed in order to investigate the effect of the variants on the whole protein expression, nuclear localization and cell overgrowth induction. We identified four CDC73/HRPT2 gene mutations, three germline (c.679_680delAG, p.Val85_Val86del and p.Glu81_Pro84del), one somatic (p.Arg77Pro). In three cases the mutation was located within the Nucleolar Localisation Signals (NoLS). The three NoLS variants led to instability either of the corresponding mutated protein or mRNA or both. When transfected in HEK293 cells, NoLS mutated proteins mislocalized with a predeliction for cytoplasmic or nucleo-cytoplasmic localization and, finally, they resulted in overgrowth, consistent with a dominant negative interfering effect in the presence of the endogenous protein.