Global DNA Methylation Patterns and Gene Expression Associated with Obesity-Susceptibility in Offspring of Pregnant Sprague-Dawley Rats Exposed to BDE-47 and BDE-209
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Persistent organic pollutants (POPs) can affect epigenetic mechanisms and obesity development. Polybrominated diphenyl ethers (PBDEs)-widely used to make flames-are one of the important POPs. Prenatal exposure to endocrine disrupting chemicals (EDCs), such as POPs, may affect global DNA methylation in long interspersed nuclear elements (LINE-1), increasing the risk of obesity later in life. Therefore, pregnant Sprague-Dawley (SD) rats were used to elucidate whether BDE-47 and BDE-209 transferred through placenta and breast milk cause epigenetic changes in LINE-1 and increase genetic susceptibility to obesity as obesogen during the developmental periods. Global DNA methylation in LINE-1 and gene expression related to obesity were measured in dams and offspring, using a methylation-sensitive high resolution melting analysis (MS-HRM) and direct bisulfite sequencing and quantitative real time polymerase chain reaction (qPCR), respectively. The results of MS-HRM showed global DNA hypomethylation patterns in LINE-1 of exposed offspring (2 of total 4) at PND 4, but bisulfite sequencing showed no difference in both the exposed and non-exposed groups. Gene expression in dams related to β-oxidation pathway and those related to adipokines showed different patterns between the two groups. On the contrary, gene expressions of offspring showed a similar pattern. Gene expressions related to β-oxidation pathway and obesity were significantly increased when compared with `at birth`, but not PPAR-α. In conclusion, this study demonstrated the possibility that co-exposure to BDE-47 and BDE-209- via the placenta and breast milk-may affect epigenetic changes and modulate gene expression levels related to obesity.
Abstract
Persistent organic pollutants (POPs) can affect epigenetic mechanisms and obesity development. Polybrominated diphenyl ethers (PBDEs)-widely used to make flames-are one of the important POPs. Prenatal exposure to endocrine disrupting chemicals (EDCs), such as POPs, may affect global DNA methylation in long interspersed nuclear elements (LINE-1), increasing the risk of obesity later in life. Therefore, pregnant Sprague-Dawley (SD) rats were used to elucidate whether BDE-47 and BDE-209 transferred through placenta and breast milk cause epigenetic changes in LINE-1 and increase genetic susceptibility to obesity as obesogen during the developmental periods. Global DNA methylation in LINE-1 and gene expression related to obesity were measured in dams and offspring, using a methylation-sensitive high resolution melting analysis (MS-HRM) and direct bisulfite sequencing and quantitative real time polymerase chain reaction (qPCR), respectively. The results of MS-HRM showed global DNA hypomethylation patterns in LINE-1 of exposed offspring (2 of total 4) at PND 4, but bisulfite sequencing showed no difference in both the exposed and non-exposed groups. Gene expression in dams related to β-oxidation pathway and those related to adipokines showed different patterns between the two groups. On the contrary, gene expressions of offspring showed a similar pattern. Gene expressions related to β-oxidation pathway and obesity were significantly increased when compared with `at birth`, but not PPAR-α. In conclusion, this study demonstrated the possibility that co-exposure to BDE-47 and BDE-209- via the placenta and breast milk-may affect epigenetic changes and modulate gene expression levels related to obesity.
참고문헌 (40)
- Schell LM, "Effects of pollution on human growth and development: an introduction", J Physiol Anthropol, 25(1), pp.103~112 (2006)
- Jaraczewska K, "Distribution of polychlorinated biphenyls, organochlorine pesticides and polybrominated diphenyl ethers in human umbilical cord serum, maternal serum and milk from Wielkopolska region, Poland", Sci Total Environ, 372(1), pp.20~31 (2006)
- Stapleton HM, "Identification of flame retardants in polyurethane foam collected from baby products", Environ Sci Technol, 45(12), pp.5323~5231 (2011)
- Costa LG, "Polybrominated diphenyl ether (PBDE) flame retardants: environmental contamination, human body burden and potential adverse health effects", Acta Biomed : Atenei Parmensis, 79(3), pp.172~183 (2008)
- Aschebrook-Kilfoy B, "Polybrominated diphenyl ethers and thyroid cancer risk in the prostate, colorectal, lung, and ovarian cancer screening trial cohort", Am J Epidemiol, 181(11), pp.883~888 (2015)
- Schug TT, "Endocrine disrupting chemicals and disease susceptibility", J Steroid Biochem Mol Biol, 127(3-5), pp.204~215 (2011)
- Tang-Peronard JL, "Endocrine-disrupting chemicals and obesity development in humans: a review", Obes Rev, 12(8), pp.622~636 (2011)
- Romano ME, "Challenges and future directions to evaluating the association between prenatal exposure to endocrine disrupting chemicals and childhood obesity", Curr Epidemiol Rep, 1(2), pp.57~66 (2014)
- Janesick A, "Obesogens, stem cells and the developmental programming of obesity", Int J Androl, 35(3), pp.437~448 (2012)
- Jin B, "DNA methylation: superior or subordinate in the epigenetic hierarchy?", Genes Cancer, 2(6), pp.607~617 (2011)
- Herrera BM, "Genetics and epigenetics of obesity", Maturitas, 69(1), pp.41~49 (2011)
- Beck CR, "LINE-1 elements in structural variation and disease", Annu Rev Genomics Hum Genet, 12, pp.187~215 (2011)
- An W, "Characterization of a synthetic human LINE-1 retrotransposon ORFeus-Hs", Mob DNA, 2(1), pp.2~ (2011)
- Ostertag EM, "Biology of mammalian L1retrotransposons", Annu Rev Genet, 35(1), pp.501~538 (2001)
- Inamura K, "Tumor LINE-1 methylation level and microsatellite instability in relation to colorectal cancer prognosis", J Natl Cancer Inst, 106(9), pp.dju195~ (2014)[DOI]
- Martin SL, "The ORF1 protein encoded by LINE-1: structure and function during L1 retrotransposition", J Biomed Biotechnol, 2006(1), pp.45621~ (2006)
- Byun HM, "Epigenetic effects of low perinatal doses of flame retardant BDE-47 on mitochondrial and nuclear genes in rat offspring", Toxicology, 328, pp.152~159 (2015)
- Wojdacz TK, "Limitations and advantages of MS-HRM and bisulfite sequencing for single locus methylation studies", Expert Rev Mol Diagn, 10(5), pp.575~580 (2010)
- Welshons WV, "Large Effects from Small Exposures. I. Mechanisms for Endocrine-Disrupting Chemicals with Estrogenic Activity", Environ Health Perspect, 111(8), pp.994~1006 (2003)
- 이덕희, "내분비교란물질과 환경성질환", 대한의사협회지, 55(3), pp.243~249 (2012), 대한의사협회
- Kersten S, "Roles of PPARs in health and disease", Nature, 405(6785), pp.421~424 (2000)
- Tugwood JD, "The mouse peroxisome proliferator activated receptor recognizes a response element in the 5' flanking sequence of the rat acyl coa oxidase gene", Embo J, 11(2), pp.433~439 (1992)
- Rosen ED, "PPAR gamma is required for the differentiation of adipose tissue in vivo and in vitro", Mol Cell, 4(4), pp.611~617 (1999)
- Memon RA, "Up-regulation of peroxisome proliferatoractivated receptors (PPAR-alpha) and PPAR-gamma messenger ribonucleic acid expression in the liver in murine obesity: troglitazone induces expression of PPAR-gamma-responsive adipose tissue-specific genes in the liver of obese diabetic mice", Endocrinology, 141(11), pp.4021~4031 (2000)
- Peraldi P, "TNF-α and insulin resistance: summary and future prospects", Mol Cell Biochem, 182(1-2), pp.169~175 (1998)
- Ogai K, "Increased level of tumor necrosis factor-alpha (TNF-alpha) on the skin of Japanese obese males: measured by quantitative skin blotting", Int J Cosmet Sci, 38, pp.462~469 (2016)
- Gelinas DS, "PPAR-alpha expression inversely correlates with inflammatory cytokines IL-1beta and TNF-alpha in aging rats", Neurochem Res, 30(11), pp.1369~1375 (2005)
- Beier K, "TNF-α downregulates the peroxisome proliferator activated receptor-α and the mRNAs encoding peroxisomal proteins in rat liver", FEBS Lett, 412(2), pp.385~387 (1997)
- Kern PA, "Adiponectin expression from human adipose tissue: relation to obesity, insulin resistance, and tumor necrosis factor-alpha expression", Diabetes, 52(7), pp.1779~1785 (2003)
- Yan WJ, "Plasma levels of adiponectin and tumor necrosis factor-alpha in children with obesity", Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 11(1), pp.47~50 (2009)
- Balistreri CR, "The role of adipose tissue and adipokines in obesity-related inflammatory diseases", Mediators Inflamm, 2010, pp.802078~ (2010)
- Dolinoy DC, "Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development", Proc Natl Acad Sci USA, 104(32), pp.13056~13061 (2007)
- Jones PA, "Functions of DNA methylation: islands, start sites, gene bodies and beyond", Nat Rev Genet, 13(7), pp.484~492 (2012)
- Kamstra JH, "Transcriptional and epigenetic mechanisms underlying enhanced in vitro adipocyte differentiation by the brominated flame retardant BDE-47", Environ Sci Techno, 48(7), pp.4110~4119 (2014)
- Dao T, "Aberrant 5'-CpG methylation of cord blood TNF alpha associated with maternal exposure to polybrominated diphenyl ethers", PloS one, 10(9), pp.e0138815~ (2015)
- Kim AY, "Obesity-induced DNA hypermethylation of the adiponectin gene mediates insulin resistance", Nat Commun, 6, pp.7585~ (2015)
- Skinner MK, "Environmental epigenetic transgenerational inheritance and somatic epigenetic mitotic stability", Epigenetics, 6(7), pp.838~842 (2011)
- Buiting K, "Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect", Am J Hum Genet, 72(3), pp.571~577 (2003)
- Perera F, "Prenatal environmental exposures, epigenetics, and disease", Reprod Toxicol, 31(3), pp.363~373 (2011)
- Waterland RA, "Epigenetic epidemiology of the developmental origins hypothesis", Annu Rev Nutr, 27, pp.363~388 (2007)
