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Copyright © 2004 by The Endocrine Society Familial PAX8 Small Deletion (c.989_992delACCC) Associated with Extreme Phenotype VariabilityLuisa de Sanctis, Andrea Corrias, Damiano Romagnolo, Tina DI Palma, Alessandra Biava, Gabriella Borgarello, Paola Gianino, Leandra Silvestro, Mariastella Zannini and Irma DianzaniDepartment of Pediatric Sciences (L.d.S., D.R., G.B., P.G., L.S.), University of Torino, 10126 Torino, Italy; Division of Pediatric Endocrinology (A.C.), Regina Margherita Children’s Hospital, 10126 Torino, Italy; Istituto di Endocrinologia e Oncologia Sperimentale-Centro Nazionale di Ricerca and Department of Cellular and Molecular Biology and Pathology (T.D.P., M.Z.), University of Naples Federico II, 80131 Naples, Italy; and Department of Medical Sciences (A.B., I.D.), Eastern Piedmont University, 28100 Novara, Italy Address all correspondence and requests for reprints to: Luisa de Sanctis, M.D., Ph.D., Centro Neonati a Rischio, Department of Pediatric Sciences, University of Torino, Piazza Polonia 94, 10126 Torino, Italy. E-mail: luisa.desanctis{at}unito.it. The PAX8 gene, mapped on 2q12-q14, encodes for a transcription factor involved in thyroid cell proliferation and differentiation. Five mutations in PAX8 have been so far described in both sporadic and rare familial forms of thyroid dysgenesis with proposed autosomal dominant inheritance, all associated with thyroid hypoplasia and/or dysfunction. Fifty-four subjects with congenital hypothyroidism detected during neonatal screening and associated with an ultrasound or scintiscan picture of thyroid dysgenesis were investigated for PAX8 mutations. The entire PAX8 coding region with exon-intron boundaries was amplified from genomic DNA, and a mutational screening was performed by denaturing HPLC followed by direct sequencing when denaturing HPLC elution abnormalities appeared. A new heterozygous deletion (c.989_992delACCC) in exon 7 causing a frameshift with premature stop codon after codon 277 was identified in a subject with thyroid hypoplasia. This mutation is the only one so far identified that lies outside the paired domain. The predicted mutant protein completely lacks the C-terminal region but contains the paired box, octapeptide, and homeodomain. It retains the ability to bind a paired-domain sequence in vitro but is transcriptionally inactive. These results provide evidence that the C-terminal region is essential for transcriptional activity. The new mutation has been inherited from the completely euthyroid mother. It was also present in a brother with slightly elevated TSH only. Thus, it is associated with thyroid dysgenesis in the proband and both euthyroidism and compensated hypothyroidism in her family. This suggests that other factors/genes may modulate phenotypic expression. This article has been cited by other articles:
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