Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia
Document Type
Article
Abstract
Background: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal-dominant vascular disorder, characterized by recurrent epistaxis, mucocutaneous telangiectases, and arteriovenous malformations (AVMs) in various visceral organs. Endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1; ALK1), receptors for transforming growth factor-β (TGF-β) superfamily, have been identified as the principal HHT-causing genes.Methods: Three unrelated Korean HHT patients and their asymptomatic as well as symptomatic family members were genetically diagnosed by sequencing whole exons and their flanking regions of ENG and ACVRL1. Functionality of an aberrant translation start codon, which is created by a substitution mutation at the 5'-untranslated region (UTR) of ENG found in a HHT family, was tested by transient in vitro transfection assay. Decay of the mutant transcripts was also assessed by allele-specific expression analysis.Results: Two ENG and one ACVRL1 mutations were identified: a known ENG mutation (c.360+1G > A; p.Gly74_Tyr120del); a novel ENG mutation (c.1-127C > T); and a novel ACVRL1 mutation (c.252_253insC; p.Val85fsX168). We further validated that the 5'-UTR ENG mutation prevents translation of ENG from the biological translation initiation site of the mutant allele, and leads to degradation of the mutant transcripts.Conclusions: This is the first experimental demonstration that a 5'-UTR mutation can prevent translation of ENG among HHT patients, and further supports the previous notion that haploinsufficiency is the primary mechanism of HHT1. Our data also underscore the importance of including exons encoding 5' UTR for HHT mutation screening. © 2011 Kim et al; licensee BioMed Central Ltd.
Publication Date
10-3-2011
Publication Title
BMC Medical Genetics
E-ISSN
14712350
Volume
12
PubMed ID
21967607
Digital Object Identifier (DOI)
10.1186/1471-2350-12-130
Recommended Citation
Kim, Mi Jung; Kim, Seon Tae; Lee, Hyoung Doo; Lee, Kyu Yong; Seo, Jiyoung; Lee, Jae Bom; Lee, Young Jae; and Oh, Suk P., "Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia" (2011). Translational Neuroscience. 679.
https://scholar.barrowneuro.org/neurobiology/679