Research Resource: Identification of Novel Coregulators Specific for Thyroid Hormone Receptor-β2
Author(s) -
Johnnie B. Hahm,
Martin L. Privalsky
Publication year - 2013
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/me.2012-1117
Subject(s) - gene isoform , biology , receptor , thyroid hormone receptor , nuclear receptor , thyroid hormone receptor beta , function (biology) , microbiology and biotechnology , transcription factor , computational biology , hormone receptor , biochemistry , genetics , gene , cancer , breast cancer
Thyroid hormone receptors (TRs) are expressed as a series of interrelated isoforms that perform distinct biological roles. The TRβ2 isoform is found predominantly in the hypothalamus, pituitary, retina, and cochlea and displays unique transcriptional properties relative to the other TR isoforms. To more fully understand the isoform-specific biological and molecular properties of TRβ2, we have identified a series of previously unrecognized proteins that selectively interact with TRβ2 compared with the more widely expressed TRβ1. Several of these proteins preferentially enhance the transcriptional activity of TRβ2 when coexpressed in cells and are likely to represent novel, isoform-specific coactivators. Additional proteins were also identified in our screen that bind equally to TRβ1 and TRβ2 and may function as isoform-independent auxiliary proteins for these and/or other nuclear receptors. We propose that a combination of isoform-specific recruitment and tissue-specific expression of these newly identified coregulator candidates serves to customize TR function for different biological purposes in different cell types.
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