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Gene screening in Japanese families with complete deficiency of thyroxine‐binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation
Author(s) -
Takeda K.,
Iyota K.,
Mori Y.,
Tamura Y.,
Suehlro T.,
Kubo Y.,
Refetoff S.,
Hashimoto K.
Publication year - 1994
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 - 10.1111/j.1365-2265.1994.tb02472.x
Subject(s) - thyroxine binding globulin , biology , mutation , radioimmunoassay , allele , gene , medicine , genetics , microbiology and biotechnology , endocrinology , polymerase chain reaction , hormone , triiodothyronine
Summary OBJECTIVE Thyroxine‐binding globulin (TBG) is a serum protein that transports 75% of circulating thyroxine. Eleven naturally occurring mutations in the human TBG gene have been identified, ten of which alter the properties of the molecule. Three of these mutations produce complete deficiency of TBG (TBG‐CD) and four are associated with a second mutation in codon 283 (TBG‐poly) which is polymorphic in some ethnic groups but, when present alone, does not alter the properties of the TBG molecule. In this communication we investigate whether two unrelated Japanese families with TBG‐CD harboured the TBG‐CD J mutation in codon 352 associated with TBG‐CD in families residing in more distant locations of the Japanese Islands. In addition we examined the possible association with TBG‐poly and its incidence in the Japanese population. DESIGN Mutant alleles were identified by amplification of genomic DNAs by the polymerase chain reaction, using altele‐specific oligonucleotide primers. PATIENTS Eight family members and 25 normal subjects. MEASUREMENTS Serum free thyroxine and TBG concentration were measured by a conventional radioimmunoassay and a more sensitive enzyme immunoassay. Genomic DNAs were extracted from white blood cells and specific mutations at codons 352 and 283 were identified by allele‐specific amplification. RESULTS Three males and three females, whose serum TBG levels were decreased, had mutations at codon 352 as hemizygous and heterozygous, respectively. This mutation was not present in the DNA of any of the related or unrelated subjects with normal TBG concentration. The presence of TBG‐poly was demonstrated in only one heterozygous family member and in six out of 30 alleles (20%) in normal unrelated subjects. The frequency of this TBG polymorphism in the Japanese is similar to that of 16% reported in French Canadians. CONCLUSIONS We conclude that TBG‐CDJ might be a prevalent cause of complete deficiency of thyroxine‐binding globulin in the Japanese and that TBG‐poly probably appeared before the divergence of human races.