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Originally published In Press as doi:10.1074/jbc.M707059200 on September 27, 2007

J. Biol. Chem., Vol. 282, Issue 48, 34653-34662, November 30, 2007
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Altered RNA Binding Activity Underlies Abnormal Thyroid Hormone Metabolism Linked to a Mutation in Selenocysteine Insertion Sequence-binding Protein 2*

Jodi L. Bubenik{ddagger} and Donna M. Driscoll{ddagger}§1

From the {ddagger}Department of Cell Biology, Lerner Research Institute, Cleveland Clinic and the §Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case Western University, Cleveland, Ohio 44195

The expression of selenoproteins requires the translational recoding of the UGA stop codon to selenocysteine. In eukaryotes, this requires an RNA stem loop structure in the 3'-untranslated region, termed a selenocysteine insertion sequence (SECIS), and SECIS-binding protein 2 (SBP2). This study implicates SBP2 in dictating the hierarchy of selenoprotein expression, because it is the first to show that SBP2 distinguishes between SECIS elements in vitro. Using RNA electrophoretic mobility shift assays, we demonstrate that a naturally occurring mutation in SBP2, which correlates with abnormal thyroid hormone function in humans, lies within a novel, bipartite RNA-binding domain. This mutation alters the RNA binding affinity of SBP2 such that it no longer stably interacts with a subset of SECIS elements. Assays performed under competitive conditions to mimic intracellular conditions suggest that the differential affinity of SBP2 for various SECIS elements will determine the expression pattern of the selenoproteome. We hypothesize that the selective loss of a subset of selenoproteins, including some involved in thyroid hormone homeostasis, is responsible for the abnormal thyroid hormone metabolism previously observed in the affected individuals.


Received for publication, August 22, 2007 , and in revised form, September 26, 2007.

* This work was supported by Public Health Services Grant HL29582 from the National Institutes of Health (to D. M. D.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 To whom correspondence should be addressed: Dept. of Cell Biology, Lerner Research Institute, 9500 Euclid Ave., NC10, Cleveland, OH 44195. Tel.: 216-445-9758; Fax: 216-444-9404; E-mail: driscod{at}ccf.org.


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