» Articles » PMID: 24499025

The Effect of Dietary Fat Intake on Hepatic Gene Expression in LG/J AND SM/J Mice

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2014 Feb 7
PMID 24499025
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The liver plays a major role in regulating metabolic homeostasis and is vital for nutrient metabolism. Identifying the genetic factors regulating these processes could lead to a greater understanding of how liver function responds to a high-fat diet and how that response may influence susceptibilities to obesity and metabolic syndrome. In this study we examine differences in hepatic gene expression between the LG/J and SM/J inbred mouse strains and how gene expression in these strains is affected by high-fat diet. LG/J and SM/J are known to differ in their responses to a high-fat diet for a variety of obesity- and diabetes-related traits, with the SM/J strain exhibiting a stronger phenotypic response to diet.

Results: Dietary intake had a significant effect on gene expression in both inbred lines. Genes up-regulated by a high-fat diet were involved in biological processes such as lipid and carbohydrate metabolism; protein and amino acid metabolic processes were down regulated on a high-fat diet. A total of 259 unique transcripts exhibited a significant diet-by-strain interaction. These genes tended to be associated with immune function. In addition, genes involved in biochemical processes related to non-alcoholic fatty liver disease (NAFLD) manifested different responses to diet between the two strains. For most of these genes, SM/J had a stronger response to the high-fat diet than LG/J.

Conclusions: These data show that dietary fat impacts gene expression levels in SM/J relative to LG/J, with SM/J exhibiting a stronger response. This supports previous data showing that SM/J has a stronger phenotypic response to high-fat diet. Based upon these findings, we suggest that SM/J and its cross with the LG/J strain provide a good model for examining non-alcoholic fatty liver disease and its role in metabolic syndrome.

Citing Articles

Use of a ferroptosis-related gene signature to construct diagnostic and prognostic models for assessing immune infiltration in metabolic dysfunction-associated fatty liver disease.

Lian X, Tang X Front Cell Dev Biol. 2023; 11:1199846.

PMID: 37928903 PMC: 10622674. DOI: 10.3389/fcell.2023.1199846.


Maternal exposure to high-fat diet during pregnancy and lactation predisposes normal weight offspring mice to develop hepatic inflammation and insulin resistance.

Saengnipanthkul S, Noh H, Friedline R, Suk S, Choi S, Acosta N Physiol Rep. 2021; 9(6):e14811.

PMID: 33769706 PMC: 7995551. DOI: 10.14814/phy2.14811.


Hepatocyte expression of the micropeptide adropin regulates the liver fasting response and is enhanced by caloric restriction.

Banerjee S, Ghoshal S, Stevens J, McCommis K, Gao S, Castro-Sepulveda M J Biol Chem. 2020; 295(40):13753-13768.

PMID: 32727846 PMC: 7535914. DOI: 10.1074/jbc.RA120.014381.


RNA-seq analysis of chondrocyte transcriptome reveals genetic heterogeneity in LG/J and SM/J murine strains.

Duan X, Cai L, Schmidt E, Shen J, Tycksen E, OKeefe R Osteoarthritis Cartilage. 2020; 28(4):516-527.

PMID: 31945456 PMC: 7108965. DOI: 10.1016/j.joca.2020.01.001.


Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.

Hernandez Cordero A, Gonzales N, Parker C, Sokolof G, Vandenbergh D, Cheng R Am J Hum Genet. 2019; 105(6):1222-1236.

PMID: 31761296 PMC: 6904802. DOI: 10.1016/j.ajhg.2019.10.014.


References
1.
Fernandez M, Semela D, Bruix J, Colle I, Pinzani M, Bosch J . Angiogenesis in liver disease. J Hepatol. 2009; 50(3):604-20. DOI: 10.1016/j.jhep.2008.12.011. View

2.
Turner C . Paxillin interactions. J Cell Sci. 2000; 113 Pt 23:4139-40. DOI: 10.1242/jcs.113.23.4139. View

3.
Stunkard A, Sorensen T, Hanis C, Teasdale T, Chakraborty R, Schull W . An adoption study of human obesity. N Engl J Med. 1986; 314(4):193-8. DOI: 10.1056/NEJM198601233140401. View

4.
Heymsfield S . How large is the energy gap that accounts for the obesity epidemic?. Am J Clin Nutr. 2009; 89(6):1717-8. DOI: 10.3945/ajcn.2009.27889. View

5.
Lyly A, Marjavaara S, Kyttala A, Uusi-Rauva K, Luiro K, Kopra O . Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism. Hum Mol Genet. 2008; 17(10):1406-17. DOI: 10.1093/hmg/ddn028. View