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Two novel mutations in the gene encoding thyroxine‐binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan
Author(s) -
Su ChingChieh,
Wu YiChi,
Chiu ChihYang,
Won Justin GingShing,
Jap TjinShing
Publication year - 2003
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1046/j.1365-2265.2003.01730.x
Subject(s) - medicine , endocrinology , missense mutation , thyroxine binding globulin , nonsense mutation , biology , gene mutation , mutation , gene , genetics , thyroid , triiodothyronine
Summary objective Thyroxine‐binding globulin (TBG) encoded by the TBG gene on chromosome Xq22 is the major transport protein, carrying approximately 75% of circulating T4. Inherited defects in TBG are associated with three phenotypes based on the level of TBG in serum of affected hemizygous males: complete TBG deficiency (TBG‐CD), partial TBG deficiency (TBG‐PD) and TBG excess (TBG‐E). In this study, we report two unrelated Han Chinese males with complete TBG deficiency who carry different mutations in the TBG gene. patients Two index cases of Han males who were diagnosed as having TBG deficiency on the basis of undetectable serum TBG and an additional 75 (50 males and 25 females) normal Han Chinese. measurement Serum thyroid hormones were measured by chemiluminescent immunoassay, thyroid autoantibodies by an agglutination test, and TSH receptor antibody and TBG by radioimmunoassay. Genomic DNA extraction, polymerase chain reaction (PCR) and DNA sequence analysis of the TBG gene were performed with standard methods. results One index case had one missense mutation in his copy of the gene, a G → A transition in codon 52 that results in the replacement of serine by asparagine, and a known polymorphism in codon 283 (TTG → TTt) that results in the replacement of leucine by phenylalanine. The allelic frequency of TBG‐Poly allele in 75 normal Han Chinese (100 chromosomes) was 31%. A second index case was hemizygous for a nonsense mutation in codon 280 of exon 3 (TGG → TGa). This mutation, located in the C‐terminal of TBG, predicts a markedly truncated protein. conclusions This is the first report of complete thyroxine‐binding globulin deficiency (TBG‐CDT1 and TBG‐CDT2) due to TBG gene mutations in Taiwan.