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Publication : Cloning of a 5.8 kb cDNA for a mouse type 2 deiodinase.

First Author  Davey JC Year  1999
Journal  Endocrinology Volume  140
Issue  2 Pages  1022-5
PubMed ID  9927339 Mgi Jnum  J:52912
Mgi Id  MGI:1330654 Doi  10.1210/endo.140.2.6678
Citation  Davey JC, et al. (1999) Cloning of a 5.8 kb cDNA for a mouse type 2 deiodinase. Endocrinology 140(2):1022-5
abstractText  From studies with their cDNAs, the types 1 and 3 deiodinases (D1 and D3) have been shown unequivocally to be selenoproteins. Studies with recently cloned cDNAs for the mammalian type 2 deiodinase (D2) indicate that they also code for selenoproteins. However, these D2 cDNAs are not full length and they do not contain an essential selenocysteine insertion sequence (SECIS) in their 3'UTR; a heterologous SECIS had to be ligated to the coding region before expression of the D2 could be achieved. Thus their role as cDNAs for the native D2 is open to question. We now report the cloning of a 5.8kb cDNA for the mouse D2. This cDNA contains a SECIS in its 3'UTR located more than 4.5 kb from die coding region. When the mRNA transcribed in vitro from this cDNA is injected into X. Laevis oocytes, a deiodinase with characteristics of D2 is expressed.
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