Regulator of G protein signaling (RGS16) inhibits hepatic fatty acid oxidation in a carbohydrate response element-binding protein (ChREBP)-dependent manner (Q28306219)

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English	Regulator of G protein signaling (RGS16) inhibits hepatic fatty acid oxidation in a carbohydrate response element-binding protein (ChREBP)-dependent manner	scientific article

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scholarly article

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Regulator of G protein signaling (RGS16) inhibits hepatic fatty acid oxidation in a carbohydrate response element-binding protein (ChREBP)-dependent manner (English)

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author name string

Victor Pashkov

1

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Jie Huang

2

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Vinay K Parameswara

3

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Wojciech Kedzierski

4

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Deborah M Kurrasch

5

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Gregory G Tall

6

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Victoria Esser

7

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Robert D Gerard

8

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Kosaku Uyeda

9

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Howard C Towle

10

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Thomas M Wilkie

11

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language of work or name

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publication date

29 April 2011

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Journal of Biological Chemistry

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286

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17

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15116-25

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Rgs16 and Rgs8 in embryonic endocrine pancreas and mouse models of diabetes

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A fasting inducible switch modulates gluconeogenesis via activator/coactivator exchange

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A humble hexose monophosphate pathway metabolite regulates short- and long-term control of lipogenesis

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Alternative splicing of RGS8 gene determines inhibitory function of receptor type-specific Gq signaling

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Evolution of the regulators of G-protein signaling multigene family in mouse and human

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Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1

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RGS proteins provide biochemical control of agonist-evoked [Ca2+]i oscillations

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20 March 2017

Mechanisms governing subcellular localization and function of human RGS2

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20 March 2017

GTPase-activating proteins for heterotrimeric G proteins: regulators of G protein signaling (RGS) and RGS-like proteins

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20 March 2017

Plasma membrane localization is required for RGS4 function in Saccharomyces cerevisiae

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20 March 2017

GAIP and RGS4 are GTPase-activating proteins for the Gi subfamily of G protein alpha subunits

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Deficiency of carbohydrate response element-binding protein (ChREBP) reduces lipogenesis as well as glycolysis

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20 March 2017

Glucose induces FGF21 mRNA expression through ChREBP activation in rat hepatocytes

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20 March 2017

The glucagon receptor is required for the adaptive metabolic response to fasting

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A glucose-responsive transcription factor that regulates carbohydrate metabolism in the liver

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G proteins: transducers of receptor-generated signals

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3083217

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Hepatic fibroblast growth factor 21 is regulated by PPARalpha and is a key mediator of hepatic lipid metabolism in ketotic states

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Endocrine regulation of the fasting response by PPARalpha-mediated induction of fibroblast growth factor 21

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Generation of RGS8 null mutant mice by Cre/loxP system.

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G protein signaling governing cell fate decisions involves opposing Galpha subunits in Cryptococcus neoformans

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Feeding and fasting controls liver expression of a regulator of G protein signaling (Rgs16) in periportal hepatocytes

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RGS2 binds directly and selectively to the M1 muscarinic acetylcholine receptor third intracellular loop to modulate Gq/11alpha signaling

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G protein-dependent Ca2+ signaling complexes in polarized cells

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Functional specialization of different hepatocyte populations

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2 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3083217

2 June 2018

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2 June 2018

LXRs regulate the balance between fat storage and oxidation.

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https://api.crossref.org/works/10.1074%2FJBC.M110.216234

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Characteristics of fatty acid oxidation in rat liver homogenates and the inhibitory effect of malonyl-CoA

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https://api.crossref.org/works/10.1074%2FJBC.M110.216234

21 January 2018

ChREBP*Mlx is the principal mediator of glucose-induced gene expression in the liver.

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https://api.crossref.org/works/10.1074%2FJBC.M110.216234

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RGS4 binds to membranes through an amphipathic alpha -helix.

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https://api.crossref.org/works/10.1074%2FJBC.M110.216234

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Organotypic liver culture in a fluid-air interface using slices of neonatal rat and adult human tissue—a model of fibrosis in vitro

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https://pubmed.ncbi.nlm.nih.gov/21357625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutation in the N-terminal domain of RGS4 disrupts PA-conferred inhibitory effect on GAP activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/21357625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Promiscuous Coupling of Receptors to Gq Class α Subunits and Effector Proteins in Pancreatic and Submandibular Gland Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/21357625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The N-terminal domain of RGS4 confers receptor-selective inhibition of G protein signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21357625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kinetics of carnitine-dependent fatty acid oxidation: implications for human carnitine deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/21357625

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RGS Proteins Determine Signaling Specificity of Gq-coupled Receptors

1 reference

https://pubmed.ncbi.nlm.nih.gov/21357625

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M110.216234

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release_vtqq5iasa5c6diwyvzxhpyv4d4

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