Identification of a novel frameshift mutation (383insT) in the RUNX2 (PEBP2 alpha/CBFA1/AML3) gene in a Japanese patient with cleidocranial dysplasia.

Abstract:

:Cleidocranial dysplasia (CCD) is an autosomal dominant disorder due to mutations in runt-related gene 2 (RUNX2)/polyomavirus enhancer-binding protein 2alphaA (PEBP2alphaA)/core-binding factor A1 (CBFA1)/acute myeloid leukemia 3 (AML3). To investigate the RUNX2 mutations in a Japanese patient with classic CCD, we analyzed the RUNX2 gene using polymerase chain reaction (PCR)-single-strand conformation polymorphism and PCR-restriction fragment length polymorphism. The patient had hypoplasia of the clavicles, patent fontanelles, short stature, supernumerary teeth, and retention of deciduous dentition. We identified a 1-bp insertion (383insT) at codon 128 of the RUNX2 gene. The 383T insertion affects the conserved residue in the runt domain and results in premature termination in the runt domain.

journal_name

J Bone Miner Metab

authors

Goseki-Sone M,Orimo H,Watanabe A,Hamatani R,Yokozeki M,Ohyama K,Kuroda T,Watanabe H,Miyazaki H,Shimada T,Oida S

doi

10.1007/s007740170030

subject

Has Abstract

pub_date

2001-01-01 00:00:00

pages

263-6

issue

4

eissn

0914-8779

issn

1435-5604

journal_volume

19

pub_type

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