|Appears in Collections:||Aquaculture Journal Articles|
|Peer Review Status:||Refereed|
|Title:||Mapping of AF1 transactivation domains in duplicated rainbow trout glucocorticoid receptors|
Bury, Nicholas R
|Citation:||Sturm A, Bron J, Green D & Bury NR (2010) Mapping of AF1 transactivation domains in duplicated rainbow trout glucocorticoid receptors. Journal of Molecular Endocrinology, 45 (6), pp. 391-404. https://doi.org/10.1677/JME-09-0152|
|Abstract:||The glucocorticoid receptor (GR) is a ligand-dependent transcription factor mediating the genomic effects of glucocorticoids. Two activation functions (AFs) are present in the GR. While the N-terminal AF1 is ligand independent, the C-terminal AF2 overlaps with the ligand-binding domain and is ligand dependent. In this study, we have mapped AF1 in duplicated rainbow trout GRs, called rtGR1 and rtGR2, showing a limited homology (24.5%) in the N-terminal domain. Ablation of this domain from rtGR1 or rtGR2 resulted in a marked decrease (>97%) in maximal hormone-dependent transactivation, but did not affect dexamethasone-binding activity or expression levels. This suggested that, similar to the situation in the human GR (hGR), AF1 is the main AF in the trout GRs. Sequence alignments with hGR suggested a localisation of AF1 to residues 70–230 of rtGR1 and 1–119 of rtGR2. These assignments were generally confirmed in the transactivation experiments with rtGR1- and rtGR2-derived mutants showing partial deletions of their N-terminal domains. In dexamethsone-treated cells (10^-7 M, 2 h), the subcellular distribution of rtGR1 and rtGR2 mutants lacking the entire N-terminal domain, as well that of an rtGR1 mutant lacking the most N-terminal 234 amino acids, was similar to that of the corresponding wild-type GRs, suggesting that the disruption of transactivation activity was not caused by impairment of nuclear access of the mutants. Bioinformatic analyses predicted the presence of potential helical segments in the core of AF1 of rtGR1 and rtGR2, and further revealed that AF1 in rtGR1, rtGR2, and hGR shares a motif composed of hydrophobic and acidic amino acids.|
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