Structure and function of the type 3 deiodinase gene

被引:71
作者
Hernandez, A [1 ]
机构
[1] Dartmouth Coll Sch Med, Dept Med, Lebanon, NH 03756 USA
关键词
D O I
10.1089/thy.2005.15.865
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thyroid hormones (TH) are essential for normal growth and development in vertebrates, and are important for the maintenance of normal metabolic activity in most tissues of the body. Because the actions of TH result from the binding of 3,3',5'-triiodothyronine (T-3) to specific nuclear receptors in the target cell, the extent of TH action in a given cell is dependent in part on the intracellular concentration of T-3. The type 3 deiodinase (D3) is a selenoenzyme that inactivates TH by catalyzing their conversion to biologically inactive metabolites. The findings that D3 activity is very high in the pregnant uterus and fetoplacental unit, and that D3-deficient mice exhibit deficits in growth, viability, and fertility strongly suggest that D3 plays an important role in development. The D3 gene (Dio3) is preferentially expressed from the paternally inherited allele and is associated with an overlapping gene transcribed from the opposite DNA strand (Dio3os). D3 mRNA expression and D3 activity are regulated by a number of hormones and growth factors as well as by genomic imprinting. Although some genomic structures appear to mediate some of these effects, many details concerning the function of the Dio3 gene are unresolved. These include the full characterization of the Dio3 and Dio3os genes, the elucidation of the mechanisms responsible for the developmental and tissue-specific patterns observed in Dio3 allelic expression, and the response of the genes to hormones and growth factors. Knowledge of these details will be important for understanding the physiologic function of an enzyme that appears to be critical for normal mammalian development.
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页码:865 / 874
页数:10
相关论文
共 113 条
[11]   MYOCARDIAL-FUNCTION IN HYPO-THYROIDISM - RELATION TO DISEASE SEVERITY AND RESPONSE TO TREATMENT [J].
BOUGH, EW ;
CROWLEY, WF ;
RIDGWAY, EC ;
WALKER, H ;
MALOOF, F ;
MYERS, GS ;
DANIELS, GH .
ARCHIVES OF INTERNAL MEDICINE, 1978, 138 (10) :1476-1480
[12]  
BRADLEY DJ, 1992, J NEUROSCI, V12, P2288
[13]  
BRENT GA, 1994, NEW ENGL J MED, V331, P847
[14]   ''Spot 14'' protein functions at the pretranslational level in the regulation of hepatic metabolism by thyroid hormone and glucose [J].
Brown, SB ;
Maloney, M ;
Kinlaw, WB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (04) :2163-2166
[15]   A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp [J].
Buiting, K ;
Lich, C ;
Cottrell, S ;
Barnicoat, A ;
Horsthemke, B .
HUMAN GENETICS, 1999, 105 (06) :665-666
[16]   The iodothyronine selenodeiodinases are thioredoxin-fold family proteins containing a glycoside hydrolase clan GH-A-like structure [J].
Callebaut, I ;
Curcio-Morelli, C ;
Mornon, JP ;
Gereben, B ;
Buettner, C ;
Huang, S ;
Castro, B ;
Fonseca, TL ;
Harney, JW ;
Larsen, PR ;
Bianco, AC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) :36887-36896
[17]   The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a [J].
Chamberlain, SJ ;
Brannan, CI .
GENOMICS, 2001, 73 (03) :316-322
[18]   Early expression of thyroid hormone deiodinases and receptors in human fetal cerebral cortex [J].
Chan, S ;
Kachilele, S ;
McCabe, CJ ;
Tannahill, LA ;
Boelaert, K ;
Gittoes, NJ ;
Visser, TJ ;
Franklyn, JA ;
Kilby, MD .
DEVELOPMENTAL BRAIN RESEARCH, 2002, 138 (02) :109-116
[19]  
CHIZZONITE RA, 1984, J BIOL CHEM, V259, P2628
[20]   Raf and fibroblast growth factor phosphorylate Elk1 and activate the serum response element of the immediate early gene pip92 by mitogen-activated protein kinase-independent as well as -dependent signaling pathways [J].
Chung, KC ;
Gomes, I ;
Wang, DH ;
Lau, LF ;
Rosner, MR .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :2272-2281