TY - JOUR
T1 - A Bioluminescence Reporter Assay for Retinoic Acid Control of Translation of the GluR1 Subunit of the AMPA Glutamate Receptor
AU - Khatib, Thabat
AU - Whiting, Andrew
AU - Chisholm, David R
AU - Redfern, Christopher
AU - Muller, Berndt
AU - McCaffery, Peter
N1 - Open access via Springer Compact
This study received support from BBSRC grant BB/P004806/1.
PY - 2019/10
Y1 - 2019/10
N2 - Retinoic acid (RA) regulates numerous aspects of central nervous system function through modulation of gene transcription via retinoic acid receptors (RARs). However, RA has important roles independent of gene transcription (non-genomic actions) and in the brain a crucial regulator of homeostatic plasticity is RAR control of glutamate receptor subunit 1 (GluR1) translation. An assay to quantify RAR regulation of GluR1 translation would be beneficial both to study the molecular components regulating this system and screen drugs that influence this critical mechanism for learning and memory in the brain. A bioluminescence reporter assay was developed that expresses firefly luciferase under the control of the GluR1 5′ untranslated region bound by RAR. This assay was introduced into SH-SY5Y cells and used to demonstrate the role of RARα in RA regulation of GluR1 translation. A screen of synthetic RAR and RXR ligands indicated that only a subset of these ligands activated GluR1 translation. The results demonstrate the practicality of this assay to explore the contribution of RARα to this pathway and that the capacity of RAR ligands to activate translation is a quality restricted to a limited number of compounds, with implications for their RAR selectivity and potentially their specificity in drug use.
AB - Retinoic acid (RA) regulates numerous aspects of central nervous system function through modulation of gene transcription via retinoic acid receptors (RARs). However, RA has important roles independent of gene transcription (non-genomic actions) and in the brain a crucial regulator of homeostatic plasticity is RAR control of glutamate receptor subunit 1 (GluR1) translation. An assay to quantify RAR regulation of GluR1 translation would be beneficial both to study the molecular components regulating this system and screen drugs that influence this critical mechanism for learning and memory in the brain. A bioluminescence reporter assay was developed that expresses firefly luciferase under the control of the GluR1 5′ untranslated region bound by RAR. This assay was introduced into SH-SY5Y cells and used to demonstrate the role of RARα in RA regulation of GluR1 translation. A screen of synthetic RAR and RXR ligands indicated that only a subset of these ligands activated GluR1 translation. The results demonstrate the practicality of this assay to explore the contribution of RARα to this pathway and that the capacity of RAR ligands to activate translation is a quality restricted to a limited number of compounds, with implications for their RAR selectivity and potentially their specificity in drug use.
KW - RAR
KW - Retinoic acid
KW - GluR1
KW - Non-genomic
UR - http://www.mendeley.com/research/bioluminescence-reporter-assay-retinoic-acid-control-translation-glur1-subunit-ampa-glutamate-recept
UR - https://abdn.pure.elsevier.com/en/en/researchoutput/a-bioluminescence-reporter-assay-for-retinoic-acid-control-of-translation-of-the-glur1-subunit-of-the-ampa-glutamate-receptor(a78ef07e-56a4-4bc5-975f-012dfb9e5cf5).html
UR - http://www.scopus.com/inward/record.url?scp=85068168562&partnerID=8YFLogxK
U2 - 10.1007/s12035-019-1571-9
DO - 10.1007/s12035-019-1571-9
M3 - Article
C2 - 35821473
SN - 0893-7648
VL - 56
SP - 7074
EP - 7084
JO - Molecular Neurobiology
JF - Molecular Neurobiology
IS - 10
ER -