Identification of two novel splicing variants of human type II iodothyronine deiodinase mRNA

被引:22
作者
Ohba, KI [1 ]
Yoshioka, T [1 ]
Muraki, T [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Pharmacol, Sch Med, Shinjuku Ku, Tokyo 1628666, Japan
关键词
Type II iodothyronine deiodinase (DII); selenocysteine; thyroid hormone; alternative splicing; reverse transcription-polymerase chain; reaction (RT-PCR);
D O I
10.1016/S0303-7207(00)00368-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human type IT iodothyronine deiodinase (hDII) belongs to a family of selenoproteins. It catalyzes 5'-deiodination of thyroxine to generate an active thyroid hormone, 3,3',5-triiodothyronine. Two novel splice variants of hDII gene transcript; namely hDII-b and hDII-c, were identified. Three distinct DNA fragments (hDII-a-c) were amplified by a reverse transcription-polymerase chain reaction (RT-PCR) with hDII intron-spanning primers using total-RNA from human umbilical vein endothelial cell line, ECV304. The sequence of hDII-a was identical to that of previously reported hDII. hDII-b and hDII-c had an additional insertion of 108 and 242 bp, respectively. The insertion sequences were found in the intron of hDII gene, therefore, two novel exons exist between exons 1 and 2 of hDII gene. The splice sites of new exons (b and c) conserved the consensus sequences of splice acceptor and donor sites, hDII-b contains exon b with an in-frame TGA codon that may encode an extra selenocysteine. hDII-c contained exons b and c and the predicted open reading frame is interrupted by a stop codon (TAA) produced by a frame shift. RT-PCR analysis showed that hDII-a and hDII-b mRNAs are expressed in human tissues including brain, kidney, lung and trachea. The mRNA abundance of hDII-c was lower than that of hDII-a or hDII-b. Thus, the new variants of hDII transcripts suggest the presence of two short exons between exons 1 and 2 of hDII gene, and of functional Variant of hDII. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:169 / 175
页数:7
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