TY - JOUR
T1 - Splice variants of metabolic nuclear receptors
T2 - Relevance for metabolic disease and therapeutic targeting
AU - Mukha, Anna
AU - Kalkhoven, Eric
AU - van Mil, Saskia W.C.
N1 - Funding Information:
This work was financially supported by the Netherlands Organisation for Health Research and Development (ZonMW; VICI grant, grant no: 09150181910029 and Aspasia, grant 015.015.013 ).
Publisher Copyright:
© 2021 The Authors
Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Metabolic nuclear receptors are ligand-activated transcription factors which control a wide range of metabolic processes and signaling pathways in response to nutrients and xenobiotics. Targeting these NRs is at the forefront of our endeavours to generate novel treatment options for diabetes, metabolic syndrome and fatty liver disease. Numerous splice variants have been described for these metabolic receptors. Structural changes, as a result of alternative splicing, lead to functional differences among NR isoforms, resulting in the regulation of different metabolic pathways by these NR splice variants. In this review, we describe known splice variants of FXR, LXRs, PXR, RXR, LRH-1, CAR and PPARs. We discuss their structure and functions, and elaborate on the regulation of splice variant abundance by nutritional signals. We conclude that NR splice variants pose an intriguing new layer of complexity in metabolic signaling, which needs to be taken into account in the development of treatment strategies for metabolic diseases.
AB - Metabolic nuclear receptors are ligand-activated transcription factors which control a wide range of metabolic processes and signaling pathways in response to nutrients and xenobiotics. Targeting these NRs is at the forefront of our endeavours to generate novel treatment options for diabetes, metabolic syndrome and fatty liver disease. Numerous splice variants have been described for these metabolic receptors. Structural changes, as a result of alternative splicing, lead to functional differences among NR isoforms, resulting in the regulation of different metabolic pathways by these NR splice variants. In this review, we describe known splice variants of FXR, LXRs, PXR, RXR, LRH-1, CAR and PPARs. We discuss their structure and functions, and elaborate on the regulation of splice variant abundance by nutritional signals. We conclude that NR splice variants pose an intriguing new layer of complexity in metabolic signaling, which needs to be taken into account in the development of treatment strategies for metabolic diseases.
KW - Alternative splicing
KW - Isoforms
KW - Metabolic disease
KW - Metabolism
KW - Nuclear receptors
UR - http://www.scopus.com/inward/record.url?scp=85107624974&partnerID=8YFLogxK
U2 - 10.1016/j.bbadis.2021.166183
DO - 10.1016/j.bbadis.2021.166183
M3 - Article
C2 - 34058349
AN - SCOPUS:85107624974
SN - 0925-4439
VL - 1867
SP - 1
EP - 13
JO - Biochimica et Biophysica Acta - Molecular Basis of Disease
JF - Biochimica et Biophysica Acta - Molecular Basis of Disease
IS - 10
M1 - 166183
ER -